[Full text] Therapeutic Effect of Idebenone on Rats with Vascular Dementia via the | NDT – Dove Medical Press

Introduction

Vascular dementia (VD) is a heterogeneous brain disease, which is featured by cognitive impairment and cerebrovascular pathologies, with the incidence rate of at least 20% of dementia second to Alzheimers disease.1 In clinical, VD is manifested as cognitive, psychological and behavioral disorders, such as repeated questioning, irritability, depression, apathy, aggression, sleep disorders and other adverse behaviors.2 The common etiologies of VD include large artery atherosclerosis, small vessel disease, myogenic stroke and cardiovascular disorders.3 A variety of cellular signaling and regulatory mechanisms are implicated in AD, including apoptosis, oxidative stress and inflammation.4 Oxidative stress has been confirmed to be related to the pathogenesis and risk factors of VD, and antioxidant therapy might play a role in the management of VD.5 Moreover, the cognitive impairment is attributed to both vascular disease and neuroinflammation.6 At present, cholinesterase inhibitors are recognized as available therapeutic agents for VD, but these drugs may produce serious adverse reactions, such as gastrointestinal reactions, joint pain, dizziness and headache, while their ability to improve the patient remains to be determined.7 With the increasing proportion of the elderly, elucidating the molecular mechanism of VD and developing potent agents are urgent for improving the quality of life for patients and reducing the social burden.

Idebenone is an analogue of coenzyme Q10 (CoQ10), which is a lipophilic electron carrier and endogenous antioxidant existing in all cell mitochondrial membranes.8 As a kind of benzoquinone that can produce reversible redox reaction, Idebenone affects the electron balance of mitochondria.9 In vitro research has revealed that Idebenone protects mitochondrial function against amyloid beta toxicity in primary cortical neurons.10 In view of its mechanism in mitochondria, Idebenone is extensively used to treat neurodegenerative diseases and diseases associated with mitochondrial etiology.11 A previous study has demonstrated that the cognitive status of patients with cerebrovascular disease and degenerative disorders can be notably improved after receiving Idebenone treatment.12 However, whether Idebenone is involved in alleviating VD by regulating oxidative stress and neuroinflammation remains unclear.

MicroRNAs (miRs) are attractive molecules that can be used as one of the biomarkers of neurodegenerative diseases.13 For example, miR-216a upregulation is neuroprotective against ischemic injury by inhibiting apoptosis and inflammation.14 Importantly, miR-216a inhibits neuronal apoptosis in a cell model of Parkinsons disease.15 But the role of miR-216a in VD remains to be established. This study explored the effect of Idebenone on oxidative stress and neuroinflammation in VD, along with its miR mechanism, which shall shed lights on the development of pharmacotherapy for VD.

All animal protocols were strictly on the basis of the National Institutes of Health Guide for the Care and Use of Laboratory Animals. The animal ethics committee of Affiliated Hospital of Chengde Medical University approved all protocols and experimental designs. All efforts were made to minimize the animal suffering.

Healthy adult Sprague-Dawley male rats (specific-pathogen-free grade, 250300g, permit number: SCXK (Xiang) 20190004) were obtained from Hunan SJA Laboratory Animal Co., Ltd. (Changsha, Hunan, China). The rats were kept in a 12-h light/dark cycle at 25 1C.

According to a previous report,16 a VD rat model was established by permanent occlusion of bilateral common carotid arteries (CCA). Within 12 h before the operation, all rats were fasted with free access to water. Each rat was anesthetized with a mixture of 5% isoflurane and 95% oxygen, and then a mixture of 3% isoflurane and 97% oxygen was supplied through a breathing mask during the operation to maintain anesthesia. The rats were placed on the electrothermal pad to maintain the anal temperature at 37C. For VD rats, a 1.52 cm incision was made on the epidermis along the midline of the neck to separate the muscles until the common carotid artery was exposed. Two segments of CCA were ligated using No.0 silk thread, and the middle artery was blocked by electrocoagulation. The other side of the CCA was treated similarly. The sham-operated rats were treated the same as that in VD rats, but the CCA was not ligated or blocked. To avoid potential postoperative infection, the wound was washed with 20 mg/mL gentamicin sulfate solution (B540724, Sangon Biotech Co., Ltd., Shanghai, China) before wound closure. The wound was then sutured to allow the rats to recover from anesthesia and return to the cage.

There were 10 sham-operated rats and 50 VD modeling rats. Fifteen days after surgery, VD rats were arbitrarily assigned into VD group, Idebenone group (oral administration of Idebenone at 100 mg/kg daily for 3 weeks), lentiviral vector negative control (Lv-NC) group (after Idebenone administration, empty Lv-NC was injected at the 16th day after surgery), Lv-inhibitor group (after Idebenone administration, Lv inhibitor of miR-216a was injected at the 16th day after surgery), and Lv-RSK2 group (after Idebenone administration, overexpression Lv of RSK2 was injected at the 16th day after surgery), with 10 rats in each group.

Idebenone (catalogue number: HY-N0303, purity: 99.62%, CAS No.5818627-9) was purchased from Medchemexpress (Monmouth Junction, NJ, USA). The lentivirus for injection was purchased from Shanghai GenePharma Co., Ltd. (Shanghai, China) with a titer of 1 109 TU/mL. According to the previous report,17 lentivirus was injected into the CA1 region of the hippocampus. First, the rats were anesthetized by the method described previously and then placed into a stereotactic apparatus (Yuyan Instrument, Shanghai, China). Injection coordinates relative to the bregma were anteroposterior, 4.52 mm; mediolateral, 3.2 mm; dorsoventral 3.16 mm below the surface of dura using coordinates derived from the atlas of Paxinos and Watson (1997). Two L lentiviral vector was injected into CA1 region of hippocampus using a 5 L syringe with a 33-gauge tip needle (Hamilton). The needle was maintained in this position for 2 min and then withdrawn slowly to prevent solution backflow. The accuracy of injection sites was identified by stereotaxic injection of Evans blue (Sigma-Aldrich, Merck KGaA, Darmstadt, Germany) into CA1 subregion of hippocampus.

The Morris water maze (MWM) test was performed from the 36th to 42nd days after surgery to test the learning and spatial memory abilities of the rats. On day 43, rats were euthanized with an overdose of pentobarbital sodium (200 mg/kg). The specific experimental process is shown in Figure 1.

Figure 1 Flow chart of the animal experiment.

The water maze device is a black circular water tank with a diameter of 120 cm, a height of 50 cm and a water depth of 30 cm. A black platform with a diameter of 10 cm was placed in the water maze through the recording system (SMART Panlab, Harvard Bioscience, Shanghai, China). The top of the platform was about 2 cm below the water surface. The tank was divided into 4 equal parts (A-D areas) and platform area (T area). The platform was located in area A. In stage I (training phase, at day 36), each rat was gently placed in a water maze in area C to face the wall for 90 s. If the platform was not found during the training, the rats were guided to the platform and maintained for 20 s for observation and learning. In stage II (during day 37-day 41), each rat was gently placed in the water maze in area C to face the water tank wall and look for the platform. If the rats successfully found the platform and stayed in the T area for 2 s, the time was recorded. If the platform was not found within 90 s, the time was recorded as 90 s, and then the rats were guided to the platform and maintained for 20 s for observation and learning. In stage III (platform crossover phase, at day 42), the platform was removed, and each rat was gently placed in the water maze in area C. The number of times the rats crossed the T area in 90 s was recorded. The learning ability and spatial memory ability of rats were evaluated based on the latency of platform searching and the times of platform crossing.

The hippocampal tissues were collected and ground with the precooled homogenate buffer solution (137 mM NaCl, 20 mM Tris, 1% NP40, 10% glycerol, 1 mM PMSF, 10 g/mL aprotinin, 1 g/mL leupeptin, 0.5 mM sodium vanadate) with a tissue masher (Changzhou, Jiangsu, China) at 10,00015,000 r/min. Then, the tissue homogenate was centrifuged in a low-temperature and low-speed centrifuge (Beckman, Chaska, MN, USA) at 3000 r/min for 1015 min to obtain the supernatant. ELISA kits were adopted to measure the concentration of interleukin (IL)-6 (ab234570, Abcam, Cambridge, MA, USA), tumor necrosis factor- (TNF-, ab46070, Abcam), malondialdehyde (MDA, A003-1-2, Nanjing Jiancheng Bioengineering Institute, Nanjing, China) and superoxide dismutase (SOD, A001-3-2, Nanjing Jiancheng) in the supernatant of hippocampus tissue homogenate.

The brain tissues of rats were embedded in paraffin and sectioned. Paraffin-embedded sections (4 m) were dewaxed in xylene and hydrated with ethanol. After washing three times with phosphate-buffered saline (PBS), each tissue section was stained with 100 L pre-prepared hematoxylin staining solution (Sigma-Aldrich, Merck KGaA, Darmstadt, Germany) for 10 min. The excessive hematoxylin dyeing solution was removed with distilled water. The tissue sections were washed with ultrapure water, stained with eosin (Sigma-Aldrich) for 3 min, dehydrated with different concentrations of ethanol, soaked in xylene, dried, and sealed with neutral resin. Tissue sections were observed under an upright fluorescent microscope (BX53, Olympus, Tokyo, Japan).

Paraffin-embedded sections (7 m) were dewaxed and hydrated. After washing with distilled water, the sections were stained with 0.25% toluidine blue (Shanghai Zeye Biotechnology Co., Ltd., Shanghai, China) at 60C for 3 h. The remaining dyeing was washed away with ultrapure water, and then the sections were washed with 95% ethanol, dehydrated with absolute ethanol, cleared with xylene, and sealed with neutral gum. Finally, the sections were observed, and images were captured under a fluorescence microscope. The images were processed by ImageJ software (USA) to count the number of CA1 neurons per 0.1 m2 and calculate the average number of positive cells.

The effect of Idebenone treatment on expression of miR in the hippocampus of rats was analyzed using SurePrint Rat miR Microarrays (Agilent Technology Co., Ltd., Beijing, China). Three repeated experiments were carried out for each group. The procedures included pre-hybridization, hybridization, washing and imaging. Agilent DNA Microarray Scanner (P/N G2565BA) equipped with extended dynamic range software was utilized for scanning and image analysis according to the Agilent miR Microarray System with miR Complete Labeling and Hyb Kit Protocol manual (Version 2.0 P/N G4170-90,011). Feature Extraction Software 10.5 was used for data extraction from raw microarray image files using the miRNA_105_Dec08 FE protocol. GeneSpring GX (Version 10.0) software was adopted for data visualization and analysis.

Protein was extracted from cells or tissues on ice with RIPA lysis buffer (Beyotime Biotechnology Co., Ltd, Shanghai, China) for 20 min. The supernatant was obtained by centrifuging at 4C at 12,000 g for 20 min. The bicinchoninic acid kit (Thermo Fisher Scientific Inc., Waltham, MA, USA) was used to quantify the protein concentration. An equal amount of protein (50 g) was separated by electrophoresis and transferred to nitrocellulose membrane. After a 2-h blocking with 5% skim milk, the membranes were incubated with primary antibodies against RSK2 (1:1000, ab32062, Abcam), Phospho IB (Ser32) (1:1000, #2859, CST, Beverly, MA, USA), IB (1:1000, #4812, CST), Phospho-NF-B p65 (Ser536) (1:1000, #3033, CST), NF-B p65 (1:1000, #8242, CST), and GAPDH (1:1000, ab181602, Abcam) overnight at 4C. Then, the membrane was incubated with goat anti-rabbit IgG H&L (HRP) (1:10,000, ab205718, Abcam) for 1 h. Protein bands were visualized using an enhanced chemiluminescence kit (Beyotime). The protein bands were analyzed by ImageJ software, and the expression of target protein was calculated by comparing the gray value of each group with the GAPDH.

TRIzol reagent (Invitrogen, Carlsbad, CA, USA) was used for extraction of total RNA containing miR and mRNA from cells and tissues. TaqMan Advanced miRNA cDNA Synthesis Kit or SuperScript IV First-Strand Synthesis System (Thermo Fisher) was adopted for cDNA synthesis. RT-qPCR was performed with 2 SYBR Green qPCR Mix (Invitrogen) on an ABI 7900HT qPCR system (Thermo Fisher). The expression was determined using the 2-CT method with GAPDH as the internal reference of mRNA and 5S as the internal reference of miR. The primer sequences used in the experiment are shown in Table 1.

Table 1 Sequence Used for RT-qPCR

RSK2 3UTR sequence containing a potential binding site to miR-216a (WT-RSK2) and mutated binding site (MT-RSK2) were obtained from TargetScan. The above sequences were inserted into pmirGLO vector (Promega, MI, USA) to produce the report plasmid. We co-transfected the luciferase reporter plasmids with miR-216a mimic or their controls (Shanghai GenePharma Co., Ltd., Shanghai, China) into 293T cells (Fenghuishengwu, Changsha, Hunan, China) using Lipofectamine 2000 (Thermo Fisher). After 2 days of incubation, the dual-luciferase assay system (Promega) was adopted to determine the luciferase activity.

GraphPad prism 8.0 (GraphPad, San Diego, CA, USA) was used to analyze data. All the experiments were repeated three times independently, and the data were in accordance with normal distribution and showed as mean standard error of mean (SEM). Unpaired t-set was adopted for comparison between two groups, and one-way or two-way analysis of variance (ANOVA) was adopted for comparison among multi-groups, followed by Tukeys post hoc test. The p < 0.05 meant a statistically significant difference.

The VD rat model was established by bilateral CCA occlusion and treated with Idebenone. The learning ability of rats was detected by analyzing the escape latency, and the memory ability of rats was detected by analyzing the times crossing the platform (Figure 2A and B). The escape latency of sham-operated rats decreased evidently on the 2nd day and the 3rd day, and remained at a low value from the 4th to the 5th day, which indicated that the rats in the sham group had better learning ability. The escape latency of VD rats increased from the 2nd day to the 5th day, indicating that the learning ability of VD rats was significantly decreased. Compared with VD group, the escape latency of Idebenone-treated rats was notably reduced from the 3rd to the 5th day, which indicated that Idebenone treatment improved the learning ability of VD rats. In the platform crossing analysis, the time of rats crossing platform in VD group was reduced, which proved that VD modeling led to the damage of spatial memory ability of rats. However, after Idebenone treatment, the number of times the rats crossed the platform was clearly reduced. However, there was no notable difference in swimming speed among the groups, indicating that abnormal behaviors of VD rats were not related to dyskinesia (Figure 2C).

Figure 2 Idebenone ameliorates brain injury in VD rats. (A) The escape latency test examined by MWM test. (B) The spatial memory ability of rats tested by platform crossing experiment. (C) Swimming speed of rats. (D) The concentrations of oxidative stress- and inflammation-related indexes in hippocampus detected by ELISA. (E) The neuronal damage in the hippocampal cortex examined by HE staining. (F) The neuronal damage in hippocampal CA1 area of rats measured by Nissl staining. N = 10. All experiments were repeated three times independently. The results were shown as mean SEM or representative pictures. Data in panels B/D/F were analyzed by one-way ANOVA, and data in panels A/C were analyzed by two-way ANOVA. *p < 0.05, vs the sham; #p < 0.05, vs the VD.

Idebenone can inhibit oxidative stress and inflammatory damage to protect the body,1820 which are the causes of VD,21,22 so we speculated that the therapeutic effect of Idebenone was elicited on VD rats through suppressing oxidative stress and inflammatory damage. We detected the expression of MDA, SOD, IL-6 and TNF- in hippocampus by ELISA. VD modeling resulted in a significant increase in the levels of MDA, IL-6 and TNF-, and a significant decrease in the concentration of SOD. The levels of these indicators were reversed after Idebenone treatment (Figure 2D) (all p < 0.05).

To intuitively observe the nerve injury of rats, we also carried out histochemical staining. HE staining (Figure 2E) was performed on the hippocampal cortex of rats. The neurons in VD rats showed obvious disorder of arrangement and structural loss. The space between neurons was enlarged, and the nucleus showed shrinkage and unclear structure. Idebenone treatment can significantly reduce the damage of neurons induced by VD. Nissl staining of hippocampal CA1 region showed that Nissl bodies in VD rats were markedly reduced, while significantly elevated after Idebenone treatment (Figure 2F).

To study the molecular mechanism of Idebenone on VD rats, we performed microarray analysis of hippocampal tissues in VD rats and those treated with Idebenone and showed the top 10 differentially expressed miRs (Figure 3A). After Idebenone treatment, miR-216a in the hippocampus of rats was increased. According to the previous report,14 miR-216a could reduce neuroinflammation. miR-216a also plays an anti-inflammatory role in lung injury and diabetic retinopathy,23,24 and inhibits oxidative stress in asthma.25 Therefore, we speculated that the therapeutic effect of Idebenone on VD depended on miR-216a. While the expression of miR-216a in hippocampal tissues of rats in the sham-operated and VD groups was detected by RT-qPCR assay, we found that its expression was significantly reduced in VD rats (Figure 3B).

Figure 3 Inhibition of miR-216a attenuates the improvement of Idebenone on learning and spatial memory abilities in VD rats. (A) The differentially expressed miRs in hippocampus of VD group and Idebenone group screened by microarray analysis. (B) Detection of miR-216a expression in VD rats by RT-qPCR. (C) The learning ability of rats was detected by escape latency test. (D) The spatial memory ability of rats was detected by platform crossing experiment. (E) The changes of swimming speed. N = 10. All the experiments were repeated three times independently. The results showed that the average value was SEM. Unpaired t-test was used for comparison in panel B/D, and two-way ANOVA was used for comparison in panels C/E. *p < 0.05, vs Lv-NC; #p < 0.05, vs sham-operated rats.

miR-216a inhibitor encapsulated by lentivirus was injected into the brain ventricle of rats treated with Idebenone. The corresponding Lv-NC vector was used as control. The escape latency of Lv inhibitor group was increased from the 3rd to the 5th day (Figure 3C), while the times of crossing the platform were significantly lowered (Figure 3D). There was no notable difference in swimming speed between the two groups (Figure 3E).

In the Lv-inhibitor group, miR-216a expression in hippocampus was decreased (Figure 4A). ELISA assay results revealed that the concentration of MDA, IL-6, and TNF- was clearly increased, while SOD was decreased (Figure 4B). HE staining showed that the protective effect of Idebenone on hippocampal cortical neurons was evidently inhibited (Figure 4C). Nissl staining revealed that the Nissl bodies were significantly lowered after inhibition of miR-216a (Figure 4D).

Figure 4 Inhibition of miR-216a weakens the inhibitory effect of Idebenone on neuroinflammation and oxidative stress in VD rats. (A) The miR-216a expression in hippocampus of rats after injection determined by RT-qPCR. (B) The concentration of inflammation- and oxidative stress-related indicators in the hippocampus examined by ELISA. (C) The neuronal damage in the hippocampal cortex evaluated by HE staining. (D) The damage of neurons observed by Nissl staining. N = 10. All the experiments were repeated three times independently. The results showed that the average value was SEM. Unpaired t-test was used for comparison between two groups. *p < 0.05, vs Lv-NC.

The target genes of miR-216a were selected from TargetScan, miRDB and mirWalk (Figure 5A). FZD4, NAA15, RSBN1 and RPS6KA3 (also known as RSK2) were in the intersection of the three databases (Figure 5B). RT-qPCR elicited that only RSK2 expression had significant differences in the hippocampus of rats (Figure 5C).

Figure 5 miR-216a targets RSK2. (A) The potential target genes of miR-216a predicted in several bioinformatics websites. (B) The intersection of potential target genes. (C) The expression of potential target genes in rat hippocampus examined by RT-qPCR. (D) Detection of RSK2 expression in VD rats by RT-qPCR. (E) pmirGLO plasmid mapping and sequences for RSK2-WT and RSK2-MUT. (F) The luciferase activity of WT-RSK2 and MT-RSK2 tested by dual-luciferase assay. All the experiments were repeated three times independently, and the results were averaged. Unpaired t-test was used for comparison between two groups in panel D. Two-way ANOVA was used for comparison in panels C/F. &p < 0.05, vs sham-operated rats; *p < 0.05, vs the Lv-NC; #p < 0.05, vs the NC mimic; &p < 0.05, vs sham-operated rats.

We detected the expression of RSK2 in hippocampal tissues of rats in sham-operated and VD groups by RT-qPCR assay. Its expression was significantly elevated in hippocampal tissues of VD rats (Figure 5D). The potential binding sites of miR-216a and RSK2 were obtained in TargetScan, and the RSK2-MUT sequence was constructed by mutating the binding sites (Figure 5E). miR-216a mimic clearly inhibited the luciferase activity of RSK2-WT, but had no significant effect on that of RSK2-MUT (Figure 5F).

The rats treated with Idebenone were injected with lentivirus Lv-RSK2 into the ventricles, and the rats injected with Lv-NC served as controls. The learning and spatial memory abilities of rats injected with Lv-RSK2 were notably decreased (Figure 6A and B). The specific manifestations were the prolongation of escape latency and the decrease of crossing platform times. There was no significant effect of lentivirus injection on the motor ability of rats (Figure 6C).

Figure 6 Overexpression of RSK2 attenuates the therapeutic effect of Idebenone on VD rats via the IB/NF-B axis. (A) The learning ability of rats was detected by escape latency test. (B) The spatial memory ability of rats was detected by platform crossing experiment. (C) The changes of swimming speed. (D) the protein expression of RSK2, IB, P-IB, p65 and p-p65 in the hippocampus of rats detected by WB. (E) The levels of oxidative stress- and inflammation-related factors in hippocampus tissue measured by ELISA. (F) the neuronal damage in the hippocampal cortex evaluated by HE staining. (G) the neuronal damage in CA1 area of hippocampus examined by Nissl staining. N = 10. All experiments were repeated three times independently. The results were shown as mean SEM or representative pictures. Unpaired t-test was used for comparison in panels B/E/G, and two-way ANOVA was used for comparison in panels A/C/D. * p < 0.05, vs the Lv-NC.

According to the previous report,26 RSK2 can promote the phosphorylation of IB and NF-B. WB showed that RSK2 and P-IB, IB, p65, p-p65 levels were elevated in the hippocampus of rats (Figure 6D). The expression of RSK2 and phosphorylation of IB and NF-B were significantly enhanced in rats injected with Lv-RSK2. Consequently, the levels of MDA, IL-6 and TNF- in hippocampus were clearly increased, while SOD was decreased (Figure 6E).

HE staining implied that neurons in rats injected with Lv-RSK2 showed obvious pathological phenomena, such as uneven arrangement, incomplete structure and increased gap (Figure 6F). Nissl staining elicited that RSK2 overexpression reduced Nissl bodies in CA1 area of hippocampus (Figure 6G).

VD is featured by a progressive deterioration of memory and cognitive functions caused by cerebrovascular diseases.1 In recent decades, many studies have been proposed to the therapeutic potential of Idebenone in the treatment of neurodegenerative diseases.8,27 This study revealed that Idebenone exerted therapeutic effects on VD rats by repressing oxidative stress and neuroinflammation.

Emerging evidence has highlighted the critical roles of oxidative stress and neuroinflammation in the cognitive impairment in VD patients.22 Idebenone can attenuate oxidative stress and inflammatory reaction induced by titanium dioxide nanoparticles in the rat liver.19 Idebenone shows significant neuroprotective and antioxidant activities in pilocarpine-induced seizures.18 Accordingly, we speculated that Idebenone might exert therapeutic effects on VD rats by reducing oxidative stress and inflammatory reaction. Therefore, we detected the indicators relating oxidative stress and inflammation in the hippocampus of rats. After Idebenone treatment, the levels of MDA, IL-6, TNF- were decreased significantly, and the concentration of SOD was increased. Consistently, Marcus Kernt et al have revealed that Idebenone inhibits oxidative stress and apoptosis of astrocytes in human optic nerve head by stabilizing Bax/Bcl-2 ratio.28 Yan et al have clarified that Idebenone can attenuate neuroinflammation and regulate microglial polarization in a mouse model of Parkinsons disease.29 Moreover, Idebenone treatment can notably reduce the damage of neurons and increase Nissl bodies. Taken together, Idebenone mitigated brain injury in the rat model of VD.

Then, we investigated the molecular mechanism of Idebenone in VD. We analyzed the hippocampal tissues of rats in the VD group and Idebenone group by microarray analysis and screened the top ten miRs with differential expression. We found that the miR-216a expression in hippocampus was significantly elevated after Idebenone treatment. miR-216a is implicated in the tumorigenesis and progression of diverse human malignancies, such as renal cell carcinoma, breast cancer and pancreatic cancer.3032 However, the role of miR-216a in VD remains unknown yet. Intriguingly, the existing evidence indicates that elevated miR-216a can exert neuroprotective effects on cerebral ischemia injury.14 miR-216a can attenuate lipopolysaccharide-induced inflammatory injury via the JAK2/STAT3 and NF-B signaling.23 miR-216a-5p protects 16HBE cells from H2O2-induced oxidative stress by targeting the HMGB1/NF-B pathway.25 We thus speculated that the therapeutic effects of Idebenone on VD rats depend on increasing miR-216a expression. To verify our hypothesis, we injected miR-129 inhibitor into the ventricles of rats treated with Idebenone. The results exhibited that miR-216a inhibitor not only attenuated the improving effect of Idebenone on learning and spatial memory abilities, but also weakened the inhibitory effect of Idebenone on neuroinflammation and oxidative stress on VD rats. In brief, inhibition of miR-216a weakened the therapeutic effects of Idebenone on VD rats.

Thereafter, we screened the target genes of miR-216a through the database and detected their mRNA expression in the hippocampus of VD rats delivered with Lv-NC or Lv-inhibitor. We found that only RSK2 showed significant differential expression. The binding relationship between miR-216a and RSK2 was verified using dual-luciferase reporter gene assay. Activation of RSK2 promotes the inflammatory process of fibroblast-like synoviocytes.33 RSK2 is activated when microglia and THP1 monocytes are exposed to -amyloid protein, which is the main component of Alzheimers plaques.34 We conducted functional rescue experiments to prove that Idebenone improved the symptoms of VD rats via targeting miR-216a/RSK2 axis. The results exhibited that overexpression of RSK2 attenuated the therapeutic effects of Idebenone on VD. RSK2 can promote the phosphorylation of IB, thus facilitating the activation and transferring of p65 and p50 of NF-B to the nucleus.26 NF-B is a redox-sensitive transcription factor family, which has binding sites in the promoter region of amyloidogenesis and inflammation-related genes.35 The activation of NF-B results in the elevation of pro-inflammatory cytokines and proteins, which consequently causes inflammatory reaction and cell death.36 Since NF-B is implicated in the physiological inflammatory processes, it is extensively accepted as a potential target of the inflammation-based therapy for Alzheimers disease.37 Yao et al have also demonstrated that NF-B pathway may be involved in the mechanism of triptolide improving cognitive dysfunction in VD rats.38 The miR-216a/RSK2 axis regulated the therapeutic effects of Idebenone by mediating the IB/NF-B pathway.

To sum up, Idebenone ameliorated oxidative stress and neuroinflammation in VD rats via the miR-216a/RSK2/IB/NF-B axis. Our current data indicate that Idebenone has therapeutic effects on neurodegenerative diseases as a novel anti-inflammatory and antioxidant stress agent. In the future, we shall carry out more prospective studies to verify the safety and feasibility of Idebenone in the treatment of VD.

There is no funding to report.

The authors declare no potential conflicts of interest.

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