Severe acute pancreatitis-associated cardiac injury – review | JIR – Dove Medical Press

Introduction

AP is a rapid onset of abdominal inflammation, which is the most common gastrointestinal cause of hospitalization or death in China and many other countries. Most patients with mild AP recover completely after conservative treatment. However, about 20% of patients may advance to SAP,1 with rapid and persistent progression to SIRS and MODS, poor prognosis and mortality as high as 30% (Figure 1).2 The heart is one of the target organs vulnerable to pancreatic inflammation.3 Studies have shown that AP, regardless of its severity, is accompanied by cardiac injury, and the degree of injury is correlated with the clinical type of AP. Mild acute pancreatitis (MAP) is accompanied by slight myocardial injury, which is transient and can recover by itself. SAP is usually complicated with severe myocardial injury and dysfunction. At present, there is no specific or uniform definition of acute pancreatitis-associated cardiac injury. In 1971, Lovett4 first reported that acute pancreatitis could lead to myocardial dysfunction, characterized by impaired myocardial contractile function, decreased ejection fraction, poor contraction response to volume load, decreased peak systolic pressure/end-systolic volume ratio and an enlarged heart. Later, an increasing number of studies have shown that patients with pancreatitis will suffer from cardiac injury. For instance, in a prospective clinical research that recruited 52 consecutive patients with AP, electrocardiographic and echocardiographic changes were observed in more than 50% of patients with AP, and prolonged QTc interval, pericardial effusion and diastolic dysfunction were associated with higher mortality.5 Furthermore, in a study investigating the incidence of organ failure in SAP, it was found that 61.7% of the patients suffer multiple organ failure (MOF), and 26.6% had single organ failure, including the respiratory system (35.1%), the cardiovascular system (22.3%), the gastrointestinal tract (19.1%), the liver (15.9%), the kidney (14.9%), the neurologic and hematological system (8.5%).6 Likewise, in another related study, the incidence of myocardial infarction (MI) induced by SAP was as high as 60.5%.7 Other synchronized manifestations of myocardial dysfunction, such as altered cardiac input/output ratio, troponin imbalance, arrhythmia, cardiogenic shock, myocarditis and other types of MIs have also been reported in patients with SAP.810 In addition, Saulea et al11 observed obvious pathological ultrastructure damage such as microcirculation vessels destruction, interstitial edema, matrix collagenization, excessive contraction of myofibrils and cardiomyocytes hypoxia, edema and hypertrophy in the heart of experimental AP rats (Table 1).

Table 1 Characteristics of Severe Acute Pancreatitis-Associated Cardiac Injury

Figure 1 Data related to acute pancreatitis. (A and B): proportion and mortality in acute pancreatitis of different severity. (C and D): proportion and mortality of acute pancreatitis complicated with organ failure.

Worldwide, despite advances in medical treatment, imaging and interventional technology, the incidence of AP continues to increase. The incidence of AP in the United States has risen to approximately 45 per 100,000 people, while that in Britain has increased from 6.9 to 75 per 100,000 men and from 11.2 to 48 per 100,000 women.12 Cardiac injury in AP is challenging to treat, which greatly increases the death risk of AP. A comprehensive and systematic understanding of the occurrence and development of SAP-associated cardiac injury, as well as early and rapid diagnosis, are helpful for effective targeted treatment to reduce mortality. Thus, we summarize the main mechanism of myocardial dysfunction in SAP, evaluate the potential diagnostic markers, and briefly outline the current treatment strategies and potential future methods, to provide guidance of great significance for clinicians to conduct treatment work and scientific research.

The pathogenesis of SACI is hugely complex, and it is a process of inflammatory injury induced by multi-factors, multi-links and multi-organs. We summarized the pathological mechanism of SACI into the following three main links (Figure 2): 1) The local inflammation of the pancreas caused by the acinar cell injury and trypsin release in the early stage of AP give rise to the release of many inflammation-related mediators through cascade effects, leading to SIRS, laying the groundwork for subsequent organ failure (including cardiac injury). 2) The intestinal barrier is damaged, and endotoxin enters the blood, which causes infectious pancreatic necrosis and aggravates the injury of extra-pancreatic organs (including the heart) 3) The mechanism of cardiac vascular and nerve injury in SAP.

Figure 2 Pathophysiological mechanisms influencing the development of cardiac injury in SAP. Various risk factors (gallstones, alcohol, diet and drugs) cause acinar cell damage and the release of pancreatic hydrolase, leading to excessive activation and autocrine of macrophages and neutrophils, resulting in the accumulation of a large number of pro-inflammatory factors. Then the local inflammation at the lesion is amplified through the inflammatory cascade effect, which eventually results in necrosis and hemorrhage of most pancreatic tissue, releasing more and more cytokines, and induces hypercytokinemia (a cytokine storm). As the disease progresses and pancreatic inflammation involves the intestine, it causes dysfunction of intestinal barrier, which leads to the migration of intestinal flora to the pancreas and blood, followed by pancreatic infection and sepsis. These high levels of risk factors (including trypsin, endotoxin and cytokines) in the blood can damage vascular endothelial cells, trigger systemic inflammatory response, lead to myocardial microcirculatory disturbance, autonomic nerve dysfunction and abnormal autophagy, and eventually result in myocardial injury and cardiac dysfunction.

Studies at home and abroad have shown that distant organ failure caused by SAP is closely related to SIRS, in which the homeostasis imbalance caused by excessive production of trypsin, cytokines (TNF-, IL-1, IL-18 and IL-6) and inflammatory transmitters (NO, ROS and HMGB1) is the main factor of myocardial injury in AP. These inflammation-related factors regulate and induce each other and jointly cause abnormal electrical activity of cardiomyocytes, mitochondrial damage, energy metabolism disorder, systolic myocardial dysfunction, myocardial hypertrophy, fibrosis and apoptosis by activating complex signal pathway networks (Figure 3).

Figure 3 The specific pathways of myocardial injury and cardiac dysfunction caused by inflammation-related factors. DAMPs and PAMPs such as HMGB1, ATP and endotoxin from the pancreas and intestine act on membrane receptors such as TLR and P2X7R to recruit inflammatory cells (macrophages, neutrophils and dendritic cells) in serum, activate classical inflammatory pathways such as NF-B and NLRP3 inflammasome in inflammatory cells, release a large number of pro-inflammatory cytokines, and form a cascade reaction (upper). These inflammatory factors eventually act on cardiomyocytes, causing myocardial energy metabolism disorder, systolic myocardial dysfunction, myocardial hypertrophy, apoptosis and fibrosis through a complex network of signaling pathways (lower).

Pancreatin is one of the earliest mediators considered to trigger SIRS by SAP. As early as the 1950s, some scholars put forward that pancreatin could move along the tissue plane to bring about pseudocyst and tissue damage at distal organs. Such movement of pancreatin may cause direct myocardial injury,13 resulting in the increasing of cardiomyocyte permeability, secondary electrical interference and cell necrosis to destroy the structure and function of the normal myocardium. Dan et al14 measured trypsin levels in serum, jejunum, lung and heart of septic model rats, rats with a protease inhibitor (ulinastatin) and control rats. They found that trypsin levels in serum, jejunum, lung and heart of model rats were significantly higher than those in the control group and decreased significantly after administration of ulinastatin. The level of serum trypsin was negatively correlated with the expression of two intestinal barrier function-associated proteins (mucin-2 and E-cadherin) but positively correlated with inflammation indices such as TNF , IL-6 and neutrophil elastase. These data suggest that trypsin is closely related to intestinal barrier dysfunction, lung injury and heart injury during systemic inflammation. In addition, trypsin has been reported to alter platelet adhesion and affect the coagulation system, leading to coronary thrombosis and myocardial ischemia.13,15 Masuda et al16 also found that utilizing urinary trypsin inhibitor (UTI) may contribute to the recovery of cardiac function after ischemia/reperfusion (I/R) by reducing the severity of mitochondrial dysfunction and maintaining energy production during a state of shock. Similarly, Mauro et al17 proved that plasma-derived -1 anti-trypsin offers cardioprotective effects by inhibiting inflammasome activation. Besides trypsin, pancreatic lipase may also be a factor that cannot be ignored in SAP-associated cardiac injury. The presence of mature adipocytes in the myocardium is a sufficient substrate for pancreatic lipase-induced steatonecrosis. Roncati et al18 observed steatonecrosis in areas of lipomatous infiltration of the heart following acute exacerbation of latent chronic pancreatitis, but the specific injury mechanism still needs much research to support.

Relevant research found that TNF- increased obviously in serum of patients with AP, reaching the peak on the first day of MAP while on the fourth day in patients with SAP.19 Therefore, dynamic monitoring of TNF- is supposed to evaluate the severity of AP. Many experimental studies have revealed that TNF- has a negative inotropic effect on the heart in vivo,20 and this decreased contractility may be related to abnormal energy metabolism of the myocardium. Hofmann et al21 found that TNF- not only showed immediate negative inotropic effects but also increased oxygen demand in the myocardium of human right atrial. They suggest that TNF- impairs myocardial contraction by affecting the chemico-mechanical energy transduction of cardiomyocytes. On the one hand, TNF- could immediately suppress the chemico-mechanical energy transduction through the sphingosine-mediated pathway.22 On the other hand, Gellerich and Trumbeckaite23 also showed that TNF- could cause mitochondrial dysfunction and energy metabolic disorder in cardiomyocytes by inhibiting complex I and complex II activity in the mitochondrial intima. Jude et al24 further verified that TNF- has a negative inotropic effect on isolated rat hearts and can induce PKC activation, resulting in impaired cardiac contractility. More importantly, some studies19 have shown that TNF- could lead to abnormal myocardial electrical activity through NO-dependent pathway.

IL-1 belongs to IL-1 family (IL-1F), mainly produced by activated monocytes-macrophages and endothelial cells, and is involved in many systemic and acute injury reactions. Serum IL-1 levels in patients with AP were significantly increased and continued to elevate with the aggravation of AP.25 The high level of IL-1 in serum of patients with AP in the later stage may be the main cause of various cardiac injuries. Studies of Chamberlain26 and Kirii27 have demonstrated the atherogenic property of IL-1, leading to ischemic myocardial injury. Lack of IL-1 can reduce the severity of atherosclerosis in model mice, possibly achieved by decreasing the expression of vascular cell adhesion molecule 1 (VCAM-1) and monocyte chemoattractant protein 1 (MCP-1) in the aorta.28 Khoury et al29 have shown that IL-1 can also down-regulate L-type calcium channels on myocardial cell membranes, which is a determinant of action potential duration and is related to the excitation-contraction coupling of cardiac myocytes. Therefore, IL-1 can influence systolic cardiac function through calcium channels. Another study indicated that IL-1 activates caspase-3 to promote cardiomyocyte apoptosis by releasing cytochrome C (Cyt C) into the cytoplasm.30 In addition, a growing number of studies have observed a significant up-regulation of IL-1 and IL-18 in infarcted myocardium.31 This phenomenon is probably due to the release of endogenous danger signals (such as ATP) derived from injured and necrotic cardiomyocytes, which activates a strong inflammatory reaction that exacerbates and prolongs cardiac damage while removing necrotic cells and matrix debris. This intense inflammatory reaction is mediated by a protein complex called NLRP3 inflammasome.32 Nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3) inflammasome is composed of NLRP3 protein, apoptosis-associated speck-like protein containing CARD (ASC) and pro-caspase-1. When NLRP3 inflammasome is activated in response to extracellular signals, pro-caspase-1 can be cleaved and activated. Activated caspase-1 can induce cell pyroptosis and release inflammatory factors by cleaving GSDMD protein, pro-IL-1 and pro-IL-18.33

The animal study by Toldo et al34 showed that IL-1 caused a remarkable increase in IL-18, and the myocardial contractile dysfunction induced by IL-1 was attenuated after applicating IL-18 receptor blockers, suggesting that the effect of IL-1 on myocardial contractile function may be realized by up-regulating the level of IL-18. IL-18 is also a member of IL-1F, which mainly comes from monocyte-macrophages. According to the research of Janiak et al,35 the level of IL-18 in serum of patients with AP on the 1st, 3rd and 5th day after admission was significantly higher than that in the healthy control group, and the concentration of IL-18 was positively correlated with C-reaction protein (CRP). IL-18 is therefore considered to be an early indicator of the severity of AP. Mallat et al36 observed an increase in plasma IL-18 concentrations of patients with acute coronary syndromes related to the severity of myocardial dysfunction. The pathological role of IL-18 in unstable coronary artery disease and ischemic myocardial dysfunction mainly refers to the following reasons: (1) promotes atherosclerotic plaque instability and systemic inflammatory responses by activating monocytes/macrophages, lymphocytes and endothelial cells. (2) IL-18 up-regulates expression of endothelial cell adhesion molecules and generation of pro-inflammatory mediators such as IL-1, IL-8, TNF- and inducible nitric oxide synthase (iNOS), enlarging the scope of myocardial inflammatory injury.37 (3) enhances the exogenous apoptosis pathway by inducing the expression of death receptor Fas on cardiomyocyte membrane. Yoshida et al38 further verified that IL-18 could lead to myocardial necrosis and myocardial vascular endothelial injury by enhancing the effect of TNF-. Furthermore, the activated IL-18 combines with its receptors ( and subunits) to form a ligand-receptor complex which could activate the PI3K-Akt-GATA4 pathway, which leads to hypertrophy and increases osteopontin (OPN), which leads to fibrosis,39 playing a crucial role in triggering myocardial inflammation and remodeling.

Sternby et al40 analyzed 232 patients with AP, showing that the serum IL-6 concentration of SAP patients was significantly higher than that of MAP patients. Another study indicated that plasma IL-6 is implicated in the incidence of cardiovascular events in AP patients complicated with peritonitis treated by peritoneal dialysis,41 which further confirms that IL-6 may play a certain role in AP-associated cardiac injury. The bulk of the evidence suggested that IL-6 is continuously up-regulated in various experimental models of cardiac injury and heart failure.4244 IL-6 binds to the IL-6R on the surface of cardiomyocytes and subsequently associates with gp130, which dimerizing and activating Janus kinases and triggering STAT3 phosphorylation. Continuous gp130/STAT3 signaling enhanced the inflammation and myocardial hypertrophy of remodeling infarcted hearts, characterized by increased myocardial stiffness and decreased contractile force.45 Wang et al46 uncovered that IL-6 might induce cardiac fibroblast proliferation, differentiation and fibrosis by activating MMP2/MMP3 signal mediated by TGF-1. Also, IL-6 has a vital role in myocardial hypertrophy, fibrosis and apoptosis induced by angiotensin II (AngII).47

IL-10 is a natural anti-cytokine and the most important known anti-inflammatory cytokine, which can inhibit the production of TNF-, IL-1, IL-8, IL-12 and other cytokines, and the release of oxygen-free radicals.48 Zhang49 found that compared with normal control rats, the pro-inflammatory factor TNF- increased significantly, and the anti-inflammatory factor IL-10 decreased significantly in rats with SAP. After heme treatment, the oxidative stress and TNF- levels in plasma and tissues were significantly reduced, while IL-10 was significantly increased, suggesting that induction of heme oxygenase 1 (HO-1) in the early stage of SAP can regulate systemic inflammatory response by inhibiting TNF- and increasing IL-10, and prevent pancreatic and distant organs from injury. Van Laethem JL and MarchantA50 also verified the potential protective effect of IL-10 in rats with acute necrotizing pancreatitis (ANP). They found that recombinant IL-10 can reduce the severity of experimental acute pancreatitis by reducing acinar cell necrosis and TNF- gene expression, suggesting potential treatment strategies. TGF-1 has both pro-inflammatory and anti-inflammatory effects and exerts immune enhancement activity in some tissues while showing immune suppression in systemic circulation.51 Kulkarni et al52 have demonstrated that TGF-1 plays an important role in homeostatic regulation of immune cell proliferation and extravasation into tissues. They observed excessive inflammatory response in TGF-1 null mice, and a large number of lymphocytes and macrophages infiltrated many organs, especially in the heart and lungs.

TNF- and IL-1 exert enormous function on SAP-associated cardiac injury, while nitric oxide (NO) and nitric oxide synthase (NOS) are secondary agents of cardiac inhibition in SAP.53,54 Andican et al55 found NO increased in both pancreas and circulation in AP, and NO contributed to the pathogenesis of AP under oxidative stress. Extensive experimental studies have revealed the specific mechanism of NO-induced myocardial injury. According to the study of Ichinose & Buys,56 NO could induce the generation of a large number of cytotoxic substances (eg, peroxynitrite) in vivo, leading to myocardial dysfunction. Besides, DavidL57 discovered that high NO could also promote the release of inflammatory factors and the accumulation of intracellular Na+/Ca2+ in cardiomyocytes through cyclic guanosine monophosphate (cGMP) signaling pathway, thus inhibiting myocardial contraction/relaxation function. It is worth noting that experimental studies on NO role in cardiac injury also produced conflicting findings. NO can also restrict cardiac remodeling after an infarction, thus promoting cardiac protection under post-ischemic conditions. This dual effect of NO on the heart may be due to the dose-dependent effect and the regulatory effect of different NOS subtypes of NO. A low concentration of NO and a small amount of cGMP inhibited phosphodiesterase III to prevent the hydrolysis of cAMP.58 Subsequently, the activation of protein kinase A (PKA) followed by accumulated cAMP leads to the opening of Ca2+ channel in the sarcoplasmic reticulum and depolarization of myocyte membrane potential, thereby enhancing myocardial contractility. However, high NO concentration caused a corresponding increase in cGMP, activating protein kinase G (PKG) and leading to cardiac depression by blocking calcium channels in the myocardium.59 NO is mainly produced by three kinds of NOS, including inducible NOS (iNOS), neuronal NOS (nNOS) and endothelial NOS (eNOS).60 iNOS is generally believed to take part in myocardial injury under various pathological conditions such as ischemia-reperfusion injury, sepsis, aging, myocardial infarction and heart failure through cGMP-dependent and/or independent pathways. nNOS is constitutively expressed in cardiomyocytes,61 which is involved in modulating adrenergic receptor pathway.62 Myocardial nNOS expression and activity increased in failing hearts, raising the possibility of left ventricular (LV) remodeling progression and functional deterioration after myocardial infarction (MI).63 eNOS plays a potential role in regulating cardiomyocytes homeostasis, especially in the early stage of myocardial suppression. eNOS in the myocardium produces NO, which modifies calcium channel to inhibit calcium entry and induce myofibril relaxation, which has great effects on preventing myocardial dysfunction induced by sepsis.64 Likewise, alprostadil relieved myocardial ischemia/reperfusion injury by promoting antioxidant activity and eNOS activation in rats.65 All above research supported the notion that NO have different regulatory and dose-dependent effects, and there is a physiological balance among NO, superoxide and peroxynitrite in subcellular compartments. Possibly, a holistic understanding of the biological complexity and properties of NO and its derived active nitrogen species could provide a more specific and effective treatment targets for myocardial injury.

Overproduction of reactive oxygen species (ROS) is also one of the critical causes of cardiac injury in SAP. Braganza et al66 found that oxidative stress has pervaded the vascular compartment by the time of admission in patients with acute pancreatitis by analyzing admission blood samples. Wen et al67 found that the protein level and protein activity of Nox2 and Nox4 in myocardial tissue of SAP rats were significantly higher than sham-operated rats, suggesting that Nox2 and Nox4 were abnormally activated in myocardial injury induced by SAP. This elevation of these enzymes directly mediates ROS production, increases oxidative stress, promotes apoptosis and finally leads to myocardial injury. 1-oxyl-2,2,6,6-tetramethyl-4-hydroxypiperidine (tempol), a membrane-permeable radical scavenger, could significantly reduce the intensity of inflammation and oxidative stress and improve the morphological damage and exhibits anti-inflammatory and cardioprotective effects in the cerulein-induced pancreatitis rats.68 Excessive oxidation of lipid by ROS leads to serious membrane damage of cardiomyocytes. The main mechanism is that ROS attacks the unsaturated double bonds of polyunsaturated fatty acids in phospholipid of cell membrane, arouses the chain and proliferation reaction of free radicals to form a series of lipid-free radicals and the degradation products malondialdehyde, which will further reduce the fluidity and increase the permeability of cardiomyocytes membrane.69 Meanwhile, ROS-mediated lipooxidative damage is also one of the crucial mechanisms causing Ca2+ channel dysfunction. ROS can selectively act on L-type calcium channels, preventing the flow of extracellular Ca2+ into cells.70 The IP3 receptor, Ryanodine receptor and Na+-Ca2+ exchanger in endoplasmic reticulum, proteins associated with Ca2+ channel, are also regulated by redox.7173 Studies have shown that the calcium sensitivity of myocardial fibers decreases during sepsis, which may be related to the activation of ROS-related apoptosis signal-regulating kinase-1 (ASK-1) and troponin T phosphorylation.74,75 In addition, ROS initiates the transcription of many inflammatory factors by participating in the regulation of NF-B signaling pathway, which aggravates the local inflammatory reaction of myocardium.7678

Myocardial mitochondrial membranes contain more unsaturated fatty acids than other plasma membranes and are the most sensitive to lipid peroxidation.79,80 When the isolated heart tissue was exposed to the solution that produces ROS, it was observed that mitochondria seriously swelled and even disintegrated. Mitochondria dysfunction leads to impaired ATP synthesis, and this energy disorder of cardiomyocytes induces decreased contractile function.81 Furthermore, mitochondrial dysfunction resulted in long-term accumulation of oxygen-derived-free radicals, which eventually caused catastrophic destruction and functional loss of mitochondrial DNA (mtDNA), and subsequently induce cell hypertrophy, apoptosis and interstitial fibrosis by activating matrix metalloproteinases.82 Yao et al has found that a specific antioxidant targeting mitochondrion, mitochondria-targeted vitamin E (Mito-Vit-E), could significantly maintain the integrity of mtDNA, reduced the damage of mtDNA, inhibited the leakage of mtDNA into the cytoplasm, and suppressed the up-regulation of TLR9 pathway factors, MyD88 and RAGE, thus alleviating cardiac inflammation, which is a potential cardioprotective agent.83 Moreover, in myocardial injury and dysfunction, regardless of the underlying etiology, the mitochondrium will undergo significant structural and functional changes, including the opening of mitochondrial membrane permeability transition hole,84,85 the loss of membrane potential,86 the imbalance of Ca2+ homeostasis, the generation of ATP and oxygen-derived-free radicals and the release of various pro-apoptotic proteins. All the associated pro-inflammatory mediators, including mitochondrial reactive oxygen species (mtROS), mtDNA fragments, ATP and cytochrome C, enter the circulatory system to mediate inflammatory cascade reaction through different signal pathways,87 resulting in myocardial cell injury even apoptosis88 and necrosis.89

High mobility group box-1 (HMGB1) is a highly conserved non-histone protein that widely exists in the nuclei of eukaryotic cells.90 As a pro-inflammatory factor, HMGB1 has been proved to play an important role in various diseases.91,92 Under certain conditions, HMGB1 is released outside the cell to recruit and initiate innate immune cell through TLR2, TLR4 and RAGE,93 and induce TNF-, IL-1, IL-6 and other pro-inflammatory factors to promote inflammatory cell aggregation, thus amplifying local inflammation.94 In a research investigating the spatial and temporal differential expression of HMGB1 and inflammatory cytokines (TNF-, IL-1 and IL-6) in experimental SAP rats, it was found that the expression of HMGB1, as a late inflammatory factor, was later than the early inflammatory factors IL-1, TNF- and IL-6. Serum level of IL-1, TNF- and IL-6 increased rapidly at 3 h after model induction, peaked at 6 h, then decreased at 12 h, and was lower at 24 h than those at 12 h. However, the level of HMGB1 in pancreatic tissue did not change significantly at 3 h and 6 h, but increased remarkably at 12 h and maintained up to 24 h, indicating that HMGB1 may play a key role in maintaining the development of SAP.95 Many studies have demonstrated a close relationship between HMGB1 and cardiac injury in the late stage of AP. The experimental results of Xue et al96 indicate that HMGB1/TLR4 signaling pathway can induce the maturation and activation of dendritic cells (DCs), regulate the migration, adhesion and aggregation of DCs to the myocardium, stimulate the expression of surface costimulatory molecules, thus participating in myocardial ischemia/reperfusion (I/R) injury. The utilization of HMGB1 specific neutralizing antibody significantly inhibited these responses. Wang et al97 concluded through gene knockout experiment that HMGB1 changes the spleens immune microenvironment through TLR4, up-regulates CD4+ T cell ratio, CD4+/CD8+ T cell ratio and Th17 cells in the spleen, and induces myocardial inflammatory injury. Ren et al98 proposed that miR-29a-3p transferred by mesenchymal stem cells-derived extracellular vesicles plays a cardioprotective role in myocardial injury induced by SAP via down-regulating HMGB1/TLR4/Akt axis. Tzeng et al99 also discussed the effects of HMGB1 on cardiac myocytes. They found that HMGB1 had a direct negative inotropic effect on isolated cardiomyocytes, which showed that after HMGB1 (100ng/mL) treatment, the sarcomere shortening of contractile cardiomyocytes decreased by 70%, and the height of the peak Ca2+ decreased by 50% within 5 minutes (P < 0.01). The negative effects of HMGB1 on cell contractility and calcium homeostasis were partially reversible. In addition, HMGB1 induced PKC-epsilon translocation, which leads to significant inhibition of inward I-type calcium currents, indicating that HMGB1 impairs sarcomere shortening by regulating PKC-epsilon translocation to reduce membrane calcium influx and thus reduce calcium availability in cardiomyocytes. These studies suggest that HMGB1 may be a new myocardial inhibitory factor in the process of cardiac injury.

In addition to the above common inflammatory mediators, platelet-activating factor (PAF), triglyceride, and free fatty acids (FFA) also play important roles in SIRS and MOF induced by SAP. PAF is a cell surface secretion of bioactive lipid, combined with a cell surface receptor called PAF-R to produce physiological and pathological effects. Studies have shown that AP causes the release of PAF, which leads to systemic damage such as circulatory system disorders and MOF. PAF is involved in the occurrence and development of AP and is considered the key mediator of SAP, giving rise to various serious complications and high mortality. The use of platelet-activating factor receptor antagonist (PAF-RAs) can signally reduce local and systemic events after AP.100,101

Hypertriglyceridemia-associated acute pancreatitis (HTGAP) gradually increased and showed a younger, more serious trend. As early as the 1980s, it was reported that patients with HTGAP died of ischemic heart disease.102 A retrospective study also noted a significant increase in the incidence of cardiovascular events one year later in AP patients with TG level > 1000mg/dL), compared with control patients (TG < 200mg/dL).103 In addition, it has been observed that the significant increase of serum FFA in patients with acute hyperlipidemic pancreatitis is positively correlated with the severity of the disease, which is an independent risk factor for the disease to progress to SAP.104 Under aerobic conditions, long-chain FFA is the preferred metabolic substrate of the myocardium. It has been proven to be harmful both experimentally and clinically under the condition of ischemia/hypoxia, and the serum FFA level of patients with myocardial ischemia is significantly high. The possible harmful mechanisms include (1) accumulation of toxic intermediates of fatty acid metabolism, such as long-chain acyl-coenzyme, a thioester, and long-chain acylcarnitine; (2) inhibition of glucose utilization, especially glycolytic ischemia and/or reperfusion; (3) inhibition of oxidative metabolism and decoupling of electron transfer. Although the relative importance of these mechanisms is still controversial, experiments have proven that FFA metabolism inhibitors can indeed reduce the size of myocardial infarction and relieve post-ischemic cardiac dysfunction in animal models of local and systemic ischemia.105

Calcineurin is a central calcium responsive signal molecule, which can mediate the occurrence of AP. Recently, researchers have revealed its new role in AP. Wen et al106 found that calcineurin derived from hematopoiesis and neutrophils could activate immune cells to localize to the lungs and cause SIRS in AP mice. In addition, Calcineurin is also in the pancreas and promotes local inflammation of the pancreas during AP. These findings suggest a potential strategy for preventing pancreatitis and extra-pancreatic inflammation by blocking or deleting calcineurin.

The intestinal tract is one of the earliest damaged extra-pancreatic organs by SAP. Increasing evidence has highlighted the relevance of increased intestinal permeability and consequent bacterial translocation in SAP development, which leads to intestinal endotoxemia.107 Animal studies showed that compared with negative control rats, SAP rats suffered intestinal flora disorder, intestinal mucosal barrier damage, and increased plasma endotoxin concentration.108,109 In clinical trials, J Martnez,110 M A von der Mhlen111 and Anne J van der Meer112 observed that serum endotoxin level in SAP patients was significantly higher than that in MAP patients, and its level was correlated with the peak of inflammatory factors such as TNF-, IL-1, IL-6 and IL-10. Excessive production of pro-inflammatory factors may be an important factor of myocardial injury caused by endotoxin during SAP. In addition, endotoxin can also directly damage cardiomyocytes. Through injecting endotoxin into male C57BL/6 wild-type (WT) mice, Shang et al113 showed that myocardial injury induced by endotoxin might be related to the degradation of F-actin. Their data indicated that Mst1 expression was up-regulated rapidly in lipopolysaccharide (LPS)-treated heart and elevated expression of Mst1 up-regulated Drp1, which initiated mitochondrial fission. Excessive mitochondrial fission leads to mitochondrial oxidative injury, mitochondrial membrane potential reduction, mitochondrial proapoptotic elements translocation into the cytoplasm/nucleus, dysfunction of mitochondrial energy function and activation of mitochondrial apoptosis. F-actin degradation acted as an apparent downstream event of mitochondrial fission activation. Therefore, Mst1 expression, mitochondrial fission modification and F-actin stabilization may be potential therapeutic targets for endotoxin-induced myocardial injury. Wang et al114 found in an endotoxin-induced animal model that the expression of uncoupling protein in myocardial tissue increased, while myocardial energy metabolism and cardiac function decreased significantly, showing a negative correlation, suggesting that endotoxin may also accentuate myocardial injury by affecting myocardial energy metabolism. The research of Kawaguchi et al115 also supports this view. They discussed the role of 3-adrenergic receptor (3AR) in endotoxin-induced myocardial dysfunction. 3AR is closely related to energy metabolism and participates in lipolysis, glucose transport and insulin secretion. They observed cardiac dysfunction in mice within 612 hours of endotoxin injection, and the expression of 3AR in myocardial tissue increased obviously. After the administration of 3AR antagonist SR59230A, the cardiac function of mice was significantly improved, the expression levels of mitochondrial membrane protein complex and ATP were preserved, the expression of genes related to fatty acid oxidation and glucose metabolism increased significantly, while the expression of inducible nitric oxide synthase (iNOS) and nitric oxide content decreased significantly. These results indicate that blocking 3AR could improve impaired energy metabolism of myocardial tissue by inhibiting iNOS expression and restore cardiac function of endotoxin-induced heart failure. Nei et al116 also found that impaired cardiomyocyte survival signaling played a crucial role in endotoxin-induced cardiac injury. They observed a significant decrease in survivin protein and a significant increase in the expressions of cleaved caspase-3 and Bcl-xL in endotoxin-induced rat myocardial tissue and further speculated that myocardial apoptosis might play a role in endotoxin-induced myocardial injury. Therefore, endotoxin can damage myocardium by enhancing the expression of inflammatory factors and leading to myocardial death via directly affecting myocardial metabolism, interfering with apoptosis and other ways.

In addition, according to a study of Shanbhag et al,117 acute pancreatitis conditioned mesenteric lymph causes cardiac dysfunction in rats independent of hypotension. They put forward a hypothesis of gut-lymph, pointing out that multiple organ dysfunction syndrome is due to release of toxic factors from the intestine into the mesenteric lymph. Additionally, they established a normotensive SAP rat model with lymphatic intervention or thoracic duct ligation to prove that mesenteric lymph from normotensive acute pancreatitis animals caused significant cardiac dysfunction, which could be prevented by thoracic duct ligation and external drainage of mesenteric lymph.

Damage-associated molecular patterns (DAMPs) and pathogen-associated molecular patterns (PAMPs), including trypsin, inflammation-related factors and endotoxin, derived from the pancreas and intestine damage vascular endothelial cells, induce autonomic nervous dysfunction and abnormal autophagy, directly or indirectly cause structural damage and cardiac dysfunction (through the blood supply, nerves and cardiomyocytes themselves).

Under various pathological conditions, myocardial microvascular injury, abnormal vasomotor regulation mechanism and increased blood viscosity will lead to changes in cardiac microcirculation and then affect myocardial perfusion, resulting in cardiomyocytes injury and cardiac dysfunction.

In the early stage of SAP, NF-B was over-activated, which triggered mononuclear phagocyte and granulocyte system, and released a large number of inflammatory factors, leading to vascular endothelial injury.38 Besides, activated neutrophils release microparticles-small plasma membrane vesicles containing myeloperoxidase during SAP, which could catalyze the generation of large amounts of oxygen-derived-free radicals and damage vascular endothelial cells widely.118

Kahrau et al119 compared the pulmonary capillary blood flow, permeability, leukocyte adhesion and alveolar septum thickness in rats with mild/edematous pancreatitis (EP) and severe/necrotizing (NP) by intravital microscopic. Compared with EP, the capillary permeability of NP was significantly increased while the blood flow was significantly decreased. The results suggest that the deterioration of AP to SAP, especially organ failure, is accompanied by severe microcirculation disturbance.

Under physiological conditions, the vasomotor function is regulated by various humoral factors, among which endothelin-1 (ET-1) secreted by vascular endothelial cells has a strong vasoconstrictor effect, and coronary artery may be more susceptible than peripheral artery.120 Also, thromboxane A2 (TXA2) with vasoconstrictive effect keeps dynamic balance with prostacyclin with vasodilating effect and regulates vascular tension together. Milnerowicz121 and Foitzik122 noticed that the average concentration of plasma ET-1 in SAP patients was higher than that in MAP patients, and therapy with a new endothelin A receptor antagonist (ET-RA) significantly reduced mortality rates in SAP, improved microcirculation and stabilized capillary permeability, reduced intravascular fluid loss and extravascular fluid sequestration and improved distant organ function (including heart, lung and kidney). Kiviniemi123 and Closa124 showed that the ratio of thromboxane A2/prostacyclin in serum of SAP experimental animals was significantly higher than that of normal control animals. Taken together, we can see that in SAP, the imbalance of various vasomotor substances may lead to coronary artery spasm and a decrease of myocardial blood flow.

In SAP, under the effects of inflammatory factors (such as TNF-), ischemia-reperfusion, and endothelin-1 mentioned above, capillary endothelium is damaged, permeability is increased, resulting in capillary leak syndrome,125 and a large amount of tissue fluid and inflammatory mucous exudates enter the third space, leading to a decrease in blood volume. Also, studies have demonstrated that thromboxane A2 (TXA2) and serum platelet-activating factor (PAF) obviously increased during SAP, and the number of platelets adhered in capillaries and venules is significantly increased, and the flow speed of platelets in capillaries is remarkably decreased.126 These changes in blood volume, vascular endothelial injury and hemodynamics contribute to microthrombus. Kellner and Robertson13 discovered the formation of coronary thrombosis in acute pancreatitis in their research which could be due to the increased levels of fibrinogen, coagulation factor VIII, D- dimer127 and platelets128 in plasma. Also possibly, following the release of trypsin into the blood, kallikrein is converted into its activated form, triggering the kinin system, resulting in the activation and supplementation of the 12 factor.129

Previous studies have confirmed that autonomic nervous dysfunction in the early stage of SAP is mainly manifested as increased sympathetic nerve activity.130 Abdominal pain is the most common symptom of pancreatitis. Because of the stimulation of pain and the decrease of blood volume, sympathetic nerve is excited. When sympathetic nerve is excited, it releases many catecholamines such as adrenaline and norepinephrine. Animal studies showed that plasma adrenergic levels were 25 times higher in rats with acute pancreatitis than those without acute pancreatitis.131 A high concentration of catecholamine could cause reversible damage to myocardial cells. Wallner et al132 have confirmed that acute catecholamine exposure could cause reversible damage to 10% of mouse cardiomyocytes. Moreover, it has been widely accepted that high cyclic catecholamines will inevitably lead to stress cardiomyopathy. In addition, the excitement of sympathetic nerve causes the activity of renin-angiotensin system to increase, and the produced Ang II plays an important role in myocardial injury and remodeling.133 Frolkis et al134 also authenticated that Ang II and TNF- may act synergistically and promote the occurrence of myocardial injury.

Moreover, Vagal reflex, which is also common in acute pancreatitis, can cause heart injury by directly acting on myocardium, indirectly changing coronary blood flow, or increasing secretion of pancreatic proteolytic enzyme. It is well known that the heart is innervated by T2-8 spinal nerve, while the gallbladder and common bile duct are innervated by T4-9 spinal nerve, and both intersect at T4-5 spinal nerve. Therefore, when there is pressure increases in the bile duct and adjacent tissues due to inflammation, it will cause coronary artery contraction spasm, sinus node excitability decrease, slow down of conduction velocity of specific systems, cardiac output decrease, blood pressure decrease, cardiac arrest and a series of severe consequences.135,136

Under normal physiological conditions, autophagy removes aging cells and proteins in vivo, and it is a self-protection mechanism of the body. Essandohs study137 found that tumor susceptibility gene 101 plays a protective role in endotoxin-induced myocardial injury by promoting autophagy of damaged mitochondria induced by Parkin/PTEN-induced kinase 1 (PINK1). However, excessive autophagy can aggravate cardiac inflammation. When severe acute pancreatitis appears systemic inflammatory syndrome, the organism is in a stress state. Strong evidence indicated138 that autophagy could lead to the death of cardiomyocytes under stress, which may be related to the over-decomposition of proteins and organelles (such as mitochondria), the degradation of survival factors and other forms of autophagy cross-talk or the over-formation of autophagic body. This dual effect of autophagy suggests that it may be closely related to cardiac injury associated with severe acute pancreatitis, but further study is needed.

Traditional myocardial injury markers such as cardiac troponin I (cTnI), brain natriuretic peptide (BNP) and creatine kinase (CK)-MB have good sensitivity in diagnosing myocardial function. However, during the occurrence and development of SAP, it may lead to multiple organ failure. The above indexes are easily affected by other complications and the diagnostic specificity of myocardial injury caused by SAP decreases. Hence, it is necessary to combine other biomarkers that can evaluate the severity of SAP to improve the directivity of these markers to myocardial injury caused by acute pancreatitis (Table 2).

Table 2 Markers with Predictive or Prognostic Value for SAP-Associated Cardiac Injury

It has been mentioned that endotoxin contributes to multiple organ failure (MOF) in acute pancreatitis. Endotoxemia is transient and may not be detected by intermittent blood sampling. On the contrary, changes of the patients endogenous antiendotoxin core antibody pool last for many days, and the depletion of this pool may be a pivotal event to determine the physiological significance of endotoxemia.

In a prospective clinical study, Buttenschoen et al139 observed that necrotising pancreatitis was accompanied by persistent endotoxemia with an extended rise in antiendotoxin antibodies. Patients with oedematous pancreatitis suffer from transient endotoxemia with a temporary increase of Ig specific for endotoxin. And Windsor et al140 measured daily the Acute Physiology Score (APS) and levels of CRP, IL-6, endotoxin, immunoglobulin (Ig) G and IgM antiendotoxin core antibodies in a series of 33 patients with acute pancreatitis and recorded the complications prospectively to explore the role of serum endotoxin and antiendotoxin core antibody levels in predicting the development of multiple organ failure in acute pancreatitis. Results showed that endotoxin was detected in the serum of 13 patients, while a significant change in levels of endogenous antiendotoxin core antibodies was detected in all patients with severe acute pancreatitis and in 28 overall. MOF developed in 7 patients, 5 of whom died. The combination of a rising APS over the first 48 h of admission and a significant fall in endogenous IgG antibody level was observed in all patients who developed MOF (7 of 7), but in only one of 16 without MOF (P = 0.00003; overall predictive value 91%). This study indicated that measuring the initial trend of APS and the concentration of endogenous IgG antiendotoxin core antibody could provide a method to identify patients with severe acute pancreatitis at high risk of developing MOF. This group may benefit from passive immunotherapy with antiendotoxin antibodies. In addition, Bose et al141 correlated endotoxemia with the severity and complications of acute pancreatitis as graded by contrast-enhanced computed tomography and Blameys criteria. The results showed that endotoxemia with a fall in antiendotoxin antibody titer predicted a poor prognosis of patients with acute pancreatitis.

High Mobility Group Box 1 (HMGB1) was discovered as a nuclear protein, but it has second life outside the cell, where it is regarded as a damage-associated molecular pattern. Extracellular HMGB1 triggers and maintains inflammatory response by inducing cytokine release and recruiting leukocytes. These characteristics make extracellular HMGB1 a key molecular target in many diseases. Noteworthy, high levels of serum HMGB1, especially the hyper-acetylated and disulfide isoforms, are sensitive biomarkers of diseases and are related to different disease stages.142

Xu et al143 discussed the correlation of HMGB1 with intestinal barrier injury and infection in patients with severe acute pancreatitis (SAP). They measured the serum levels of HMGB1, amylase, lipase and biochemical indexes in 80 SAP patients at admission. Moreover, the relationship between serum HMGB1 level and intestinal barrier injury and other clinical factors was analyzed. The results showed that the average level of serum HMGB1 in SAP patients (6.022.42 ng/mL) was significantly higher than that in healthy volunteers (1.870.63 ng/mL). Serum HMGB1 level was positively correlated with the Ranson score. The HMGB1 level in patients with infection during the clinical course, the HMGB1 levels in non-survivors were higher than those in survivors, and positively correlated with DAO activity, L/M ratio and endotoxin concentration (R = 0.484, P <0.01). All these figures indicated that HMGB1 level in patients with SAP increased significantly, which can be used as an important indicator to determine the intestinal barrier dysfunction and infection, and may have indirect implications for subsequent systemic response syndrome and multiple-organ dysfunction syndrome. Further explorations may prove the advantage of this biomarker in predicting cardiovascular complications.

ST2, a member of IL-1 receptor superfamily, has two main isoformstransmembrane ST2 (ST2L) and soluble ST2 (sST2). It is mainly expressed in Th2 cells, mast cells and fibroblasts, participating in multiple inflammatory processes and playing an immunomodulatory role. In recent years, sST2 has received extensive attention as a new marker of heart failure.

According to the study of Li,144 the serum levels of traditional myocardial injury markers cTnI, CK-MB and lactate dehydrogenase (LDH1) in SAP-associated cardiac injury model animals were markedly increased, serum sST2 level was significantly reduced. The anomalies, including serum amylase and cardiac-related enzymes, were reversed following adenovirus overexpression of sST2. Therefore, we speculate that combined measurement of serum sST2, cTnI, LDH and LDH1 could be used to evaluate the severity of myocardial injury in SAP, and overexpression of sST2 could reduce the severity of SAP and related cardiac injury. However, in another prospective clinical trial to evaluate the correlation between sST2 and the prognosis of STEMI patients receiving primary percutaneous coronary intervention, an opposite result was observed. Liu et al145 included 295 patients, and the data showed that biomarkers of myocardial cell damage and inflammation were positively correlated with sST2 levels. Higher sST2 was continuously associated with a higher risk of major adverse cardiovascular events in patients. This paradox suggests that the role of sST2 in myocardial injury is still controversial, and more clinical data are needed further to analyze the sensitivity and specificity of its diagnosis.

Pancreatitis-associated protein (PAP) was first found in pancreatic juice of rats with AP by French Keim, and it is related to the occurrence and development of AP warranted the named PAP.146 PAP plays a role in various physiological or pathological processes such as cellular immunity, cell proliferation and differentiation, anti-apoptosis, inflammation, and tissue repair.

In the study of Iovanna et al,147 98 patients with acute pancreatitis were classified into three groups according to the severity of the disease, and the serum PAP was retrospectively monitored during hospitalization to discuss whether serum PAP could be used as an indicator of the course of acute pancreatitis. Results showed that patients with mild pancreatitis had normal PAP values (<10 g/L). PAP level in necrotic pancreas was 8 times higher than that in non-necrotic pancreas. The PAP level in serum further increased when the disease worsened. It is indicated that monitoring serum PAP in patients with AP would provide a dynamic assessment of severity of the disease and anticipate the patients recovery. Furthermore, Fitzgibbons et al148 found that PAP concentrations also correlate with the severity of heart failure (HF) in a prospective clinical study. ROC curves revealed that PAP had similar sensitivity and specificity for HF admission at 6 months as BNP and equivalent predictive value for 12-month and 24-month all-cause mortality. Based on the ROC curve analysis, patients were grouped into those with a serum PAP <24 or 24 g/L. Patients with PAP 24 g/L had significantly greater BNP and CRP levels and greater 6- and 24-month all-cause mortality (p <0.05). In conclusion, PAP levels correlate with disease severity in patients with SAP and HF and are a novel prognostic marker for disease severity in the patients.

Myeloid cell trigger receptor-1 (TREM-1) belongs to a family-related natural killer cell receptor, which is basically expressed on the surface of neutrophils, monocytes and macrophages of myeloid cells. Soluble TREM-1 (sTREM-1) is a soluble form of TREM-1. The level of sTREM-1 is increased in body fluids of patients with various infections and diseases, and its increase is related to the amplification of inflammatory reaction.

Yasuda et al149 explored the role of sTREM-1 in acute pancreatitis by analyzing the clinical data of 48 patients with AP and 7 healthy controls. The results showed that serum sTREM-1 levels increased significantly in AP (63 11 pg/mL) and correlated with Ranson score (R=0.628, p < 0.001) and Acute Physiology and Chronic Health Evaluation II score (R =0.504, p <0.001). Serum sTREM-1 levels were higher in patients with early organ dysfunction than those without early organ dysfunction (101 19 vs 25 4 pg/mL, p <0.001). Incidences of early organ dysfunction in patients whose serum sTREM-1 levels were < or = 40 and >40 pg/mL were 17% and 83%, respectively (p <0.001). The usefulness of serum sTREM-1 in detecting early organ dysfunction was superior to CRP, IL-6, IL-8, Ranson score, and Acute Physiology and Chronic Health Evaluation II score. All these studies suggested that serum sTREM-1 level may be a useful marker and potential therapeutic target for early organ dysfunction in AP. In addition, by measuring sTREM-1 levels in blood samples of 838 patients with acute myocardial infarction, Wang et al150 found that patients with high sTREM-1 had an increased risk of all-cause mortality and major adverse cardiovascular event (MACE) compared with those with low sTREM-1 (P<0.001). High sTREM-1 was an independent predictor of all-cause mortality (hazard ratio, 1.978; 95% CI, 1.462 to 2.675; P<0.001) and MACE (hazard ratio, 2.413; 95% CI, 2.022 to 2.879; P<0.001). Therefore, we believe that sTREM-1 may have a certain predictive value in the prognosis of severe acute pancreatitis and associated cardiac injury.

Heart rate variability (HRV) is considered the pathological changes of sinoatrial node reflected in cardiac cycle changes and is an important index for non-invasive and quantitative evaluation of cardiac autonomic neuropathy.151 Studies have shown HRV analysis could help early diagnosis and disease prognosis in critically ill patients.152

Zhang et al153 investigated the value of admission HRV as a marker of infected pancreatic necrosis (IPN) or MODS in patients with SAP in a prospective observational study. They found that levels of low frequency (LF), low-frequency norm (nLF) and low frequency/high frequency (LF/HF) were significantly lower in SAP patients with IPN and MODS than those in patients without complications, while high-frequency norm (nHF) levels were significantly higher (P < 0.01). nHF is a good predictor of IPN and MODS, and areas under ROC curves of nHF in prediction of IPN and MODS were 0.927 and 0.821, superior to procalcitonin (AUC=0.709 and 0.722) and APACHEII (AUC=0.785 and 0.899). These results suggest that patients with SAP have sympathetic inhibition in the early stage, and HRV has been proved to be a good predictor of SAP infective pancreatic necrosis and multiple-organ dysfunction.

The treatment of SAP affects the prognosis of extra-pancreatic organs, so the treatment of primary SAP and the treatment of myocardial damage should be paid equal attention to (summary of treatment strategies can be seen in Table 3).

Table 3 Prevention and Treatment of SAP-Associated Cardiac Injury

Drugs such as somatostatin, octreotide, prostaglandin E1 (PGE1) and fentanyl could directly or indirectly inhibit the secretion of pancreatin and reduce the toxic effect of pancreatin on myocardium. Somatostatin can effectively reduce the internal and external secretion of the pancreas and the pressure in the pancreatic duct,154 and somatostatin pretreatment can improve the hemodynamic state of the body by reducing the release of cytokines.155 PGE1 can strongly inhibit pancreatic exocrine secretion, stabilize lysosomal membrane in acinar cells, restrict intracellular pancreatin activation, and prevent the dissolution and destruction of pancreatic cells.156 Zhang et al157 discovered the protective effect of octreotide on SAP rat heart by comparing the concentration of inflammatory indexes in blood, and pro-apoptotic proteins (Bax, Bcl-2 and Caspase-3) in myocardium and the pathological changes of the heart of SAP rats and octreotide treated rats. Wang et al158 found that fentanyl could significantly improve the swollen and disordered cardiac fibers and congested vessels in SAP rats by regulating NF-B signaling pathway and markedly inhibit the up-regulation of IL-1/ IL-6 induced by SAP.

Although the concept of early non-surgical treatment of SAP has been widely accepted, surgical interventions and endoscopy required for the etiological treatment are still fundamental measures to prevent the disease and its progress. For example, obstructive biliary pancreatitis and the abdominal compartment syndrome resulting from SAP need timely endoscopic retrograde cholangiopancreatography (ERCP) or surgical treatment.159,160 In addition, some studies proposed that abdominal paracentesis drainage (APD) therapy can play a protective role in SAP-induced myocardial injury via inhibiting HMGB1-mediated oxidative stress. Wen and his team161 found that APD could significantly improve the morphological changes of cardiomyocytes, alleviate cardiac dysfunction, reduce myocardial enzymes and cardiomyocyte apoptosis, decrease the expression of pro-apoptotic Bax and cleaved caspase-3 protein. Moreover, APD remarkably reduced the serum level of HMGB1, inhibited Nox expression, and alleviated cardiac oxidative injury.

Hypoperfusion induced by hypovolemia leads to vascular endothelial cell injury and apoptosis, increasing capillary permeability and releasing many inflammatory mediators that aggravate systemic organ damage. Reasonable and timely fluid resuscitation is the basis for preventing vascular endothelial cells from releasing inflammatory mediators. Studies have shown that combining different resuscitation fluids (saline, hydroxyethyl starch and glutamine) is more efficient in SAP resuscitate by reducing inflammation and sustaining the intestinal barrier.162 It is worth noting that the symptoms of AP are complex. In the choice of fluid therapy, we need to implement targeted treatment according to the different conditions of patients to prevent patients from MODS. Excessive fluid therapy will aggravate the fluid retention of patients, give rise to cardiac overload, resulting in acute heart failure. Huang et al163 discussed possible factors causing abnormal heart failure after successful fluid resuscitation on AP patients. They found that older patients with AP had more severe organ failure or more organ involvement and had more interstitial fluid accumulation during fluid resuscitation. Furthermore, aggressive resuscitation is associated with the development of acute kidney injury in AP.164 In recent years, it has been proposed that fluid resuscitation via the rectum can effectively improve hemodynamic disorders and organ dysfunction (jejunum, liver and lung) in SAP compared with intravenous fluid resuscitation, which may be a potential supplementary fluid management in the early stage of SAP.165 In addition, pancreatic hypoxia, microcirculation disorder and even microthrombus formation can aggravate the release of cytokines, so it is necessary to improve pancreatic anoxia and prevent microthrombus generation based on adequate fluid resuscitation. Dextran,166 Salvia miltiorrhizae167 and PGE1 can increase pancreatic blood flow, reduce hemorrhage and necrosis of the pancreas, decrease pancreatic capillary permeability, alleviate endothelial cell injury and inhibit cytokine release.156 Pancreatitis complicated with oxidative stress results in the rapid accumulation of cytokines in the body, so antioxidant therapy is important.168 Drugs commonly clinically include reduced glutathione, high-dose of vitamin C, N- acetamide cysteine, selenium, vitamin E and others.

Recently, blood purification therapy has been applied clinically to treat cytokine-induced pathological effects, but this must be done within 72 hours of onset to achieve good curative efficacy. Early continuous blood purification can reduce pro-inflammatory cytokines, prevent MODS and significantly improve the prognosis of patients with severe sepsis.169 In addition, high-flow short-time hemofiltration should be used for SAP because long-time hemofiltration can cause excessive release of IL-10 to inhibit immune function and increase the susceptibility of patients to infection. However, high-flow continuous hemofiltration is recommended for fulminant pancreatitis.170

Pancreatitis, a retroperitoneal inflammation, damaged intestinal mucosal barrier function, leading to migration of bacteria and endotoxin into the liver, heart, lung and other parts of the body, which exacerbate the release of extra-pancreatic cytokines.171 Unclipping the intestinal tract, removing toxins accumulated in the intestinal tract and nourishing the intestinal tract after dredging can significantly reduce infectious complications (IPN and sepsis) and improve survival rate.172 Rhubarb or decoction containing rhubarb, such as Dachengqi decoction and Qingyi decoction, has a certain effect on reducing intestinal flora and endotoxin translocation.173

Although the early application of prophylactic antibiotics is still controversial, most studies report that preventive antibiotics can effectively reduce infectious complications and mortality. Because early infection with pancreatitis is more likely to cause intestinal bacterial translocation, it is suggested to choose antibiotics with a high concentration in the pancreas that can cross the blood-pancreas barrier to prevent infection and reduce endotoxin production avoid the expansion of systemic inflammatory response.174 Such drugs include the third- and fourth-generation cephalosporins, and carbapenems.

With the development of critical care medicine, ulinastatin has been widely recognized in preventing MOF. Wang et al demonstrated in a rat model of myocardial infarction that high-dose ulinastatin could reduce total cholesterol, catalase, glutathione peroxidase and superoxide dismutase in myocardial tissue, thereby relieving inflammation and preventing rats from myocardial infarction.175 Similarly, Tian et al showed that ulinastatin combined with rhubarb could reduce the release of inflammatory factors such as TNF- and IL-6, change the percentage of lymphocytes to reduce organ damage induced by sepsis, improve the prognosis of patients.176 In addition, ulinastatin can decrease the secretion of inflammatory mediators by inhibiting trypsin, elastase, fibrinolytic enzyme and hyaluronidase,177 and has the functions of stabilizing lysosomal membrane and scavenging oxygen-free radicals.178

In acute pancreatitis, various direct and indirect factors cause coronary artery contraction and spasm, resulting in myocardial ischemia/reperfusion injury. Statins function as an anti-inflammation and anti-coagulation. It also regulates cellular immunity, improves endothelial cell function and resists oxidative stress.179 According to Yu et al,180 rosuvastatin can ameliorate myocardial histopathological changes and reduce MI area in isoproterenol-induced MI model in rats. Compared with the model group, the antioxidant level in the drug group was significantly increased, and the activity of NLRP3 inflammasome was decreased. These results indicate that rosuvastatin can alleviate myocardial injury by inhibiting NLRP3 inflammasome and relieving oxidative stress. In a related study, Ke et al181 showed that regulatory T cells contribute to the rosuvastatin-induced protective effect against myocardial ischemia-reperfusion injury.

Heart failure is the final stage of heart disease caused by various factors (including pancreatitis), and volume overload is the core of its pathophysiology. Clinically, diuretics (including loop diuretics, thiazide diuretics and glucocorticoid receptor antagonists) are often used to promote the excretion of water and sodium in the kidney to alleviate symptoms. They play pharmacological effects by dilating the renal artery, increasing the renal blood flow, inhibiting the reabsorption of sodium and chlorine in the renal tubules, and maintaining the balance of water and salt in the body.182 Attention, it has been reported that diuretics could induce acute pancreatitis (DAP), of which thiazides are the most common. The direct toxic effects of furosemide and pentamidine on pancreatic acinar cells lead to degeneration and necrosis of glandular cells and trypsin activation.183 The common clinical inducing doses were chlorothiazide 25~100mg/d, chlortalidone 50mg/d and furosemide 40mg~80mg/d. The corresponding symptoms usually occur within 35 weeks after medication. Most people have typical AP manifestations, but a few people only have a slight increase in amylase activity (1.5~2 times). Very few patients may have sudden shock or death. Therefore, the clinical application of diuretics in heart failure caused by acute pancreatitis needs more standardized management and more evidence-based medicine.

The Surviving Sepsis Campaign recommended norepinephrine as the first choice of vasopressor to correct septic shock. If patients need more vasoconstrictors to maintain adequate blood pressure, epinephrine can be added or replaced. Dobutamine is recommended for recurring cardiac dysfunction.184 It has been reported that milrinone,185 a second-generation dipyridone cardiotonic drug with high efficiency and low toxicity, can reduce the levels of TNF- and IL-1 in rat cardiomyocytes and regulate inflammatory mediators and cytokines. Additionally, because of its dual effects of anti-inflammatory and anti-apoptotic functions, it can improve myocardial perfusion and promote hemodynamic stability. Levosimendan186 is a non-digitalis positive inotropic drug, which can improve hemodynamics and has the advantages of not causing calcium overload, myocardial oxygen consumption and arrhythmia.

Many Traditional Chinese Medicines have the characteristics of antagonizing endotoxin and inflammatory mediators, so they play an important role in various inflammatory, metabolic and autoimmune diseases. The efficacy of various Chinese Medicines has been demonstrated in a model of rat AP induced by retrograde injection of 5% sodium taurocholate into the pancreaticobiliary duct, which resulted in an obvious injury of tissue structure and infiltration of inflammatory cells. Salvia miltiorrhizae,167 baicalin,157 Qingyi decoction,187 Lai Fu Cheng Qi decoction188 and other Chinese herbal medicine preparations significantly reduced serum inflammatory factors and myocardial injury-related indicators, and effectively improve the peripheral microcirculation, promote fluid resuscitation, heighten myocardial contractility, and reduced the mortality SAP-induced MI. Moreover, Sheng-jiang powder189 is supposed to have a protective effect on multiple-organ inflammatory damage in AP in rats fed with a high-fat diet.

AP, acute pancreatitis; SAP, severe acute pancreatitis; ANP, acute necrotizing pancreatitis; SIRS, systemic inflammatory response syndrome; MODS, multiple-organ dysfunction syndrome; MOF, multiple-organ failure; CI, cardiac injury; DAMPs, damage-associated molecular patterns; PAMPs, pathogen-associated molecular patterns; I/R, ischemia/reperfusion; LPS, lipopolysaccharide; HMGB1, high mobility group box-1; DCs, dendritic cells; IL, interleukin; VCAM-1, vascular cell adhesion molecule 1; MCP-1, monocyte chemoattractant protein 1; Cyt C, cytochrome C; NLRP3, nucleotide-binding oligomerization domain-like receptor protein 3; ASC, apoptosis-associated speck-like protein containing CARD; CRP, C-reaction protein; iNOS, inducible nitric oxide synthase; NO, nitric oxide; AngII, angiotensin II; HO-1, heme oxygenase-1; cGMP, cyclic guanosine monophosphate; PKA, protein kinase A; PKG, protein kinase G; ECG, electrocardiogram; LV, left ventricular; ROS, reactive oxygen species; ASK-1, apoptosis signal-regulating kinase-1; mtDNA, mitochondrial DNA; PAF, platelet-activating factor; FFA, free fatty acids; ET-1, endothelin-1; TXA2, thromboxane A2; cTnI, cardiac troponin I; BNP, brain natriuretic peptide; CK, creatine kinase; TREM-1, myeloid cell trigger receptor-1; PGE1, prostaglandin E1; ERCP, endoscopic retrograde cholangiopancreatography; APD, abdominal paracentesis drainage; HRV, heart rate variability; IPN, infected pancreatic necrosis; HTGAP, hypertriglyceridemia-associated acute pancreatitis.

The pathophysiology of myocardial dysfunction caused by SAP is unclear, and scientific investigations on its mechanism are still very scarce. However, some inspiration and guidance can be obtained from the pathogenesis of myocardial injury caused by sepsis. Trypsin, inflammatory mediators, ROS, endotoxin, vascular disorders, and autonomic nerves play important roles in the pancreas-heart axis. At present, there are no specific drugs used clinically to prevent SAP from progressing to MI, and the focus of treatment remains supportive and targets improving systemic inflammatory response. Currently, timely, diverse and combined treatment methods have been adopted for the myocardial injury caused by SIRS. However, due to the complexity of SAP-related MI (not only mediated by SIRS), these treatment methods and strategies are not fully applicable, and the mortality rate remains high. Therefore, it is extremely urgent to explore the pathogenesis of myocardial injury associated with acute pancreatitis and develop specific drugs targeting its molecular level.

This work was supported by The key project of the National significant R&D Program Intergovernmental Cooperation in International Science and Technology Innovation (grant number 2019YFE0119300) and National Natural Science Foundation of China (grant number 82074158).

Yalan Luo, Zhaoxia Li and Peng Ge are co-first authors. The authors declare that there are no conflicts of interest.

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Severe acute pancreatitis-associated cardiac injury - review | JIR - Dove Medical Press