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    Roles of Histone Acetylation in Aging

    HUANG Bo-yue, YANG Bao-xue
    ACTA NEUROPHARMACOLOGICA 2021, 11 (2): 53-64. DOI:10.3969/j.issn.2095-1396.2021.02.010
    Abstract182 PDF(1480KB)( 38

    As a complex multi-factor biological processaging is characterized by the gradual decline of cell homeostasistissue function and body health over time. Aging weakens the gene expression control regulated by epigenetic factors. Histone modification is a key regulatory factor that controls chromatin structure and gene transcriptionthereby affecting various important cellular biological processes. More and more studies have shown that histone acetylation under various environmental stimuli is involved in the regulation of translationwhich affects gene expression and lifespan. In this reviewwe summarize the mechanisms of histone acetylation in gene regulation and senescencedescribe the direct or indirect roles of histone acetylation in the aging-related gene expression and signaling pathwaysand discuss the potential of histone acetylation as therapeutic targets against aging.

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    Establishment and Evaluation of the Spinal Cord Injury Model in Rats

    QIAN Qi-bing, WANG Jin-ying, ZHAO Chen-yu, et al
    ACTA NEUROPHARMACOLOGICA 2021, 11 (2): 21-25. DOI:10.3969/j.issn.2095-1396.2021.02.005
    Abstract115 PDF(3010KB)( 8

    ObjectiveTo prepare and evaluate the model of acute spinal cord injurySCIin ratsso as to lay a foundation for exploring the mechanism of SCI secondary reaction and the early intervention of SCI repair. MethodsThe male SD rats aged 10 weeks were randomly divided as SCI group and Sham groupn=12. In SCI groupthe thoracic vertebrae laminectomy was performed at the 9-11ththoracic vertebraeT9-11. At T10the spinal cord was completely clamped with an aneurysm clamp50 g for 40 s),to prepare the acute SCI model in rats. The rats in Sham group only underwent laminectomy at T9-11. After SCIthe hindlimb motor function of rats was evaluated according to BBB scores. HE staining and TUNEL staining were respectively conducted to detect the pathological changes and cell apoptosis of spinal cord tissue. The relative content of proteins closely related to cell apoptosis was detected by Western blot. ResultsThe BBB scores of motor function in SCI group were significantly lower than those in Sham groupHE staining showed that the spinal cord structure of SCI group was severely damagedcell body contractedintercellular space became increasedand gray matter cavities were obviously seenThere was no abnormal change in Sham group. TUNEL staining demonstrated that the rate of cell apoptosis in SCI group was significantly higher than that of Sham groupWestern blot results showed that SCI significantly decreased the relative content of Bcl-2but increased the relative content of Bax and caspase-3. ConclusionThe SCI model prepared with an aneurysm clip compression could reflect the pathophysiology of the injured spinal cords. In view of the stability and simplicity of the model makingthe clip compression should be widely recommended in the research of SCI repair.

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    Study on Nerve Function Injury Induced by Dazolam and Its Mechanism
    YANG Rong, SUN Zhen-qin, XIE Wen-juan, NIE Bin, SUN Fu-bang
    ACTA NEUROPHARMACOLOGICA 2021, 11 (3): 5-9. DOI:10.3969/j.issn.2095-1396.2021.03.002
    Abstract89 PDF(5646KB)( 8
    Objective:To investigate the neurologic impairment induced by sedative midazolam and its mechanism. Methods:72 rats were divided into normal saline control group,midazolam group,dexmedetomidine group,each group contained 24 rats. Neuron specificity enolization enzyme(NSE),central nervous specificity protein (S100β),cell death receptor level of Fas,escape latency,swimming speed,through the original number were compaied in three groups. The pathological sections of NSE,S100β and Fas were analyzed. Results:In midazolam group,the levels of NSE,S100β and Fas were higher,the escape latency was longer,and the number of passing through the original platform was less( P<0.05). Conclusion:Midazolam has a significant effect on neurological impairment and learning and memory functions.
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    Studies on the Role of Focal Adhesion Kinase in Diseases
    HE Jin-zhao, YANG Bao-xue
    ACTA NEUROPHARMACOLOGICA 2021, 11 (3): 50-64. DOI:10.3969/j.issn.2095-1396.2021.03.009
    Abstract86 PDF(1251KB)( 22
    Focal adhesion kinase (FAK) as a crucial component of focal adhesions (FAs) plays an important role in intracellular and extracellular signal transduction. FAK is a non-receptor tyrosine kinase and mainly regulated by integrins,growth factors and G-protein-coupled receptors,which mediates various bioactivities,such as cell migration,invasion,proliferation,differentiation and angiogenesis. A wide array of studies have demonstrated that abnormal expression and activation of FAK were critically involved in the pathogenesis of cardiovascular diseases,hepatic and renal injuries,lipometabolism,immunoregulation and cancer,in which were closely related to poor prognosis. In recent years,with the development of FAK animal models and inhibitors,targeting FAK has been recognized as new treatment for diseases. Most FAK inhibitors show promising preclinical effect
    without significant adverse effect and several are undergoing clinical trials. This review summarizes the studies on the role of FAK in diseases and related animal models and inhibitors to clarify the underlying mechanism and therapeutic prospect.
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    Research Progress of Cortical Spreading Depression
    ZHAO Bo, YU Ai-mei, ZOU Yu-an
    ACTA NEUROPHARMACOLOGICA 2022, 12 (3): 28-. DOI:10.3969/j.issn.2095-1396.2022.03.006
    Abstract85 PDF(1210KB)( 27
    Cortical spreading depression is an inhibitory band of electrical activity generated after the cerebral cortex is stimulated. This inhibitory band can rapidly destroy and depolarize the concentration gradient of transmembrane ions in the cerebral cortex,resulting in short circuits inside and outside cells,which can affect brain perfusion and metabolism.resulting in a poor prognosis. This paper will summarize the research progress of CSR from the following aspects.
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    Clinical Observation on Emotion, Cognition and Abnormal Sensation of Limbs in Parkinson’s Disease combinde with Type 2 Diabetes Mellitus

    PAN Yan-ting, ZHANG Xiao-jie, FAN Lei, LIU Xing-liang, YUE Bing-hong
    ACTA NEUROPHARMACOLOGICA 2021, 11 (4): 1-. DOI:10.3969/j.issn.2095-1396.2021.04.001
    Abstract79 PDF(1082KB)( 20

    ObjectiveTo study the emotioncognition and abnormal sensation of limbs in Parkinson’s disease combined with type 2 diabetes mellitus.MethodsForty patients with Parkinson’s disease without diabetes were selected as control groupand forty patients with Parkinson’s disease combined with type 2 diabetes mellitus were selected as observation group in the same period. Analysis the difference in emotioncognition and abnormal sensation of limbs between the control group and observation group.ResultsThe result of emotion and cognition showed that the incidence of memory lossinattention and apathy was singnificantly higher in observation group than control groupP<0.05. The sensation symptoms of limbs showed that limb pain and limb cold was singnificantly higher in observation group than control groupP<0.05.ConclusionThe incidence rate of emotioncognitive impairmentnumbness and cold symptoms in Parkinson’s patients with type 2 diabetes was higher than that in PD patients without diabetes.

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    A Preliminary Study on the Effect of 5-HT2A/D2 Receptor Balancing Antagonist NH809 on Schizophrenia
    YU Min-quan, XU Xiang-qing
    ACTA NEUROPHARMACOLOGICA 2022, 12 (3): 1-. DOI:10.3969/j.issn.2095-1396.2022.03.001
    Abstract74 PDF(1284KB)( 31
    Objective:To investigate the pharmacological effects of 5-HT2A/D2 receptor balancing antagonist NH809 on schizophrenia in vivo. Methods:The effects of NH809 on schizophrenia in vivo were evaluated by MK-801 hydrogen maleat(0.3 mg·kg -1,ip) induced hyperactivity model in mice,apomorphine (1 mg·kg -1,sc) induced climbing model in mice and conditioned avoidance response(CAR) in rats,and compared with risperidone. Results:NH809 had dose-dependent inhibitory effect on MK-801 hydrogen maleate induced high activity model,apomorphine-induced climbing behavior in mice and conditioned avoidance response in vivo,with ED50 of 0.04,0.05 and 0.24 mg·kg -1,respectively. The ED50 of risperidone in these three models were 0.06,0.68 and 0.60 mg·kg -1,respectively. Conclusion:NH809 has significant pharmacological effects on several animal models of schizophrenia,and its activity in vivo is better than risperidone.
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    The Neuroprotective Effect of Ginsenoside Compound K on Neurodegenerative Diseases

    JIANG Yan, XU Jie, DONG Yang-yang, ZHAO Li-yan, ZHANG Wan-ming
    ACTA NEUROPHARMACOLOGICA 2021, 11 (4): 49-. DOI:10.3969/j.issn.2095-1396.2021.04.009
    Abstract73 PDF(1201KB)( 6

    In recent yearsthe incidence and mortality of neurodegenerative diseases have increased with the acceleration of population aging in Chinasuch as Alzheimer’s diseasevascular dementiaParkinson’s diseaseischemia cerebral vascular diseaseepilepsy and so on. Ginseng is a traditional herb in Chinawhich has the effects of anti-agingcalming the mind and promoting intelligence. Ginsenoside is the main active ingredient in ginseng. Ginsenoside compound K is the metabolite of protopanaxadiol ginsenoside in the intestine. It was found that CK has neuroprotective effects. The neuroprotective mechanism of CK was involved in antioxidant stressanti-inflammationincreased energy metabolismanti-autophagyantiapoptosisregulation of neurotransmitters and so on. Here we review the neuroprotective effect of CK on neurodegenerative diseases and the neuroprotective mechanism of CKin order to provide theoretical reference for the treatment and research and development of drugs for neurodegenerative diseases.

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    Regulation of Mitochondrial Autophagy and Its Role in Cerebral Ischemia-Reperfusion Injury
    XIE Jia-jia, SUN Ting, ZHANG Dan-shen
    ACTA NEUROPHARMACOLOGICA 2021, 11 (3): 43-49. DOI:10.3969/j.issn.2095-1396.2021.03.008
    Abstract72 PDF(1118KB)( 9
    As a regulatory mechanism involved in cell metabolism and organelle renewal,autophagy plays an important role in the physiological and pathological processes of the body. Mitophagy,as a type of cell target-specific autophagy,can identify and remove functionally impaired mitochondria and achieve mitochondrial quality control. Mitochondria mainly regulate autophagy through Parkin-dependent and non-Parkin-dependent pathways,thereby affecting the body’s function. Studies have shown that mitochondrial autophagy is closely related to the process of cerebral ischemia-reperfusion injury,but its role in cerebral ischemia-reperfusion injury has been controversial. This article mainly summarizes the mechanism of mitochondrial autophagy and the way in which mitochondrial autophagy participates in cerebral ischemia-reperfusion injury.
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    Denosumab in the Treatment of Rheumatoid Arthritis
    ZHANG Mei, WEI Wei
    ACTA NEUROPHARMACOLOGICA 2022, 12 (2): 35-. DOI:10.3969/j.issn.2095-1396.2022.02.007
    Abstract72 PDF(1144KB)( 0
    Osteoporosis is a common complication of rheumatoid arthritis (RA). Denosumab,a human antibody against receptor activator of nuclear factor-kappa B ligand,can suppress the differentiation and activation of osteoclast,increase bone mineral density (BMD), and reduce the incidence of fracture. Denosumab can be used in the treatment of rheumatoid arthritis. In the patients with RA,it can efficiently increase bone mineral density,suppress the progression of bone erosion,but it does not affect synovitis and disease activity. The combination of denosumab and disease-modifying anti-rheumatic drugs,can inhibit bone erosion synergistically with good tolerance and no increases in infection rates. We should concern about rare side effects,such as osteonecrosis of the jaw and atypical femoral fracture. Calcium and vitamin D supplementation with denosumab treatment is beneficial to prevent hypocalcemia. We should pay attention to the risk of bone mineral density decline and vertebral fractures after drug discontinuation. Denosumab discontinuation might be considered under the guidance of doctors. Administration of a bisphosphonate after denosumab discontinuation is recommended.
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    Differentiation of CD4+CD25-T Cells to Regulatory T Cells induced by Diosgenin in CIA Mice

    LIANG Xiu-jun, YU Yong-zhou, XIA Dong-shuai, GAO Ya-xian, SUN Tong-you
    ACTA NEUROPHARMACOLOGICA 2021, 11 (2): 5-10. DOI:10.3969/j.issn.2095-1396.2021.02.002
    Abstract69 PDF(2913KB)( 5

    ObjectiveTo investigate the roles of diosgenin in the differentiation of regulatory T cells from CD4+CD25-T cells in collagen induced arthritis mice. Methods

    CD4+CD25-T cells of CIA mice isolated by immunomagnetic beads on magnetic activated cell sorting device were co-cultured with different concentrations of diosgenin2512.56.25μmol·L-1for 48 hours. The ratio of Treg cells was tested by flow cytometry. The level of Foxp3 mRNA was measured by Real-Time PCR. The level of serum IL-10 was detected by ELISA. ResultsThis study separated CD4+CD25-T cells of 93.89% purity. The ratio of Treg cellsthe level of IL-10 and Foxp3 mRNA were increased significantly in diosgenin groups compared with those in control groupP<0.05. ConclusionDiosgenin may induce the differentiation of CD4+CD25-T cells to regulatory T cells in CIA mice and up-regulate the expression of Foxp3.

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    Study on Association of CD14 -159C/T and Cardiovascular Disease in the Han Nationality from Zhangjiakou
    ZHOU Lu-jin, CUI Si-yao, CHEN Su-yan, et al
    ACTA NEUROPHARMACOLOGICA 2021, 11 (6): 1-. DOI:10.3969/j.issn.2095-1396.2021.06.001
    Abstract68 PDF(11193KB)( 2
    Objective:To investigate the correlation between the physicochemical properties,functions and gene polymorphisms of the protein encoded by the cluster of differentiation antigen 14(CD14) gene and cardiovascular disease,so as to provide basis for the prevention and treatment of cardiovascular disease. Methods:Plasma samples were collected from 75 patients with cardiovascular disease (including 42 male patients and 33 female patients),and 125 healthy controls (including 80 male patients and 45 female patients). Genomic DNA was extracted from their venous blood. The polymorphism of - 159C / T (rs2569190) locus of CD14 gene was detected by polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP),and the results of enzyme digestion were observed by electrophoresis. The correlation between the polymorphism of-159C/T and cardiovascular disease was detected by genotype frequency. The physical and chemical properties,structure,function and interaction of CD14 gene coding protein were analyzed by bioinformatics methods to demonstrate the relationship between CD14 gene coding protein and cardiovascular disease. Results:The distribution frequency of TT genotype of CD14-159C / T(rs2569190) in the diseased group was 56%,which was significantly higher than that in the normal control group (40.8%). The difference was statistically significant( P<0.05),and the other genotypes were not statistically significant (P>0.05). CD14 is a secretory protein,located in the extracellular matrix,without transmembrane region and weak hydrophilicity. There were more irregular curls in the secondary structure of CD14 protein (41.87%). CD14 interacts directly with 10 proteins and plays an important role in Toll like receptor 4 signaling pathway and MyD88 dependent toll like receptor signaling pathway. Conclusion:The-159C/T( rs2569190) TT genotype of CD14 gene is closely related to the occurrence of cardiovascular disease. CD14 protein may play an important role in the occurrence and development of cardiovascular disease.
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    Progress in Clinical Application of SGLT2 Inhibitors
    ZHAO Peng-tao, LI Jia-cheng, YAN Xiao-dong, et al
    ACTA NEUROPHARMACOLOGICA 2021, 11 (5): 52-. DOI:10.3969/j.issn.2095-1396.2021.05.009
    Abstract66 PDF(1112KB)( 1
    Diabetes mellitus is a metabolic disease with abnormally high blood glucose as the main clinical manifestation. The absence or relative insufficiency of insulin is the main mechanism of diabetes mellitus. Currently,the mainstream treatment methods are to increase the body’s glucose use and enhance insulin sensitivity and insulin volume to control blood glucose.Sodium glucose co-transporter 2 inhibitor is a new oral drug for the clinical treatment of type 2 diabetes mellitus. Currently,as a second-line adjuvant in the clinical treatment of diabetes,it is different from the hypoglycemic mechanism of traditional insulin and has attracted attention.With the application of clinical treatment,the clinical researchers found SGLT2 inhibitor not only in the treatment of type 2 diabetes show strong hypoglycemic effect,at the same time,in patients with diabetes with or without cardiovascular,critical organs such as liver and kidney damage also have additional protection,SGLT2 inhibitor organ protection mechanism is not clear,however,is associated with a significant side effects,with the deepening of research,the function and mechanism of SGLT2 inhibitor is further found. This paper mainly summarized the role of SGLT2 inhibitor in lowering blood glucose,improving cardiocerebrovascular disease,kidney injury protection,anti-tumor and other aspects,as well as the potential organ protection mechanism.
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    Mechanism of Action of Traditional Chinese Medicine and Its Effective Components in Treating Epilepsy

    ZHU Xiao-que, ZHANG Wei
    ACTA NEUROPHARMACOLOGICA 2021, 11 (2): 45-52. DOI:10.3969/j.issn.2095-1396.2021.02.009
    Abstract60 PDF(1098KB)( 12

    Epilepsy is a chronic nervous system disease characterized by repeated occurrence caused by abnormal discharge of neurons in the brain. It has the characteristics of repeatabilityunpredictability and unprovoked attacks. Traditional Chinese medicine has been paid more and more attention because of its stable curative effect and small side effects in the treatment of epilepsy. In this paperwe reviewed the mechanisms of several traditional Chinese medicines in treating epilepsy for further autiepileptic drug development.

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    Effect of Huangqi Granules on Apoptosis of Hippocampal Tissue in Alzheimer’s Rats

    YE San-chuan
    ACTA NEUROPHARMACOLOGICA 2021, 11 (2): 11-14. DOI:10.3969/j.issn.2095-1396.2021.02.003
    Abstract60 PDF(1883KB)( 5

    ObjectiveTo investigate the effect of Huangqi granule on apoptosis of hippocampus in rats with Alzheimer’s disease. MethodsForty-eight healthy male SD rats were selected and randomly divided into 4 groupscontrol groupmodel groupHuangqi granule group and piracetam groupwith 12 rats in each group. The rat model of Alzheimer’s disease was established by injectingβ-amyloid peptide 1-40 into the ventricle of the rat. Astragalus granule group and piracetam group were given Astragalus granules and piracetam tablets dissolved in normal salinerespectively. The control group and model group were given the same amount of normal saline. After 30 days of treatmentthe Morris water maze method was used to determine the number of times of crossing and the escape latency of each group of SD rats to determine the learning and memory ability. Western Blot experiment was used to determine the apoptosisinhibiting protein Bcl-2 in the hippocampal tissue cells of each groupand the levels of proapoptotic proteins Bax and Caspase-3. The apoptosis of hippocampus was detected by flow cytometry. ResultsCompared with the model group of ratsthe administration of Huangqi granules and positive drugs would increase the number of traversing and shorten the escape latency of rats. The results were statistically differentP<0.05. The levels of anti-apoptotic protein Bcl-2 in the hippocampal tissue cells of the astragalus granule group and the piracetam group increased significantlywhile the levels of pro-apoptotic proteins Bax and Caspase-3 decreased significantly. The results of flow cytometry showed that the apoptosis level of Huangqi granule group was significantly lower than that of model group. ConclusionAstragalus granules can increase the level of Bcl-2 protein in the hippocampal tissue cells of Alzheimer’s disease rats and decrease the level of Bax and Caspase-3 protein to hinder the process of neuronal apoptosisthereby improving the ability of learning and memory.

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    Research Progress of Mitochondrial Permeability Transition Pore in Cerebral Ischemia-Reperfusion Injury

    SUN Ting, XIE Jia-jia, ZHANG Dan-shen
    ACTA NEUROPHARMACOLOGICA 2021, 11 (2): 26-31. DOI:10.3969/j.issn.2095-1396.2021.02.006
    Abstract59 PDF(1032KB)( 2

    Ischemic cerebrovascular disease is one of the main diseases threatening human health. Restoring blood and oxygen supply to brain tissue as soon as possible is an effective means to save patients’ lives and reduce disability rate. Howeverafter restoring blood and oxygen supply to brain tissuemore serious injury may occurnamely cerebral ischemiareperfusion injuryI/R. As an important organelle for energy productionmitochondria are very important for the survival of neurons. Among the many potential mechanisms of mitochondrial dysfunctionthe opening of mitochondrial permeability transition poremPTPhas attracted more and more attention in recent years. mPTP is a key node mediating brain dysfunction and cell death. This paper systematically summarizes the research status of mitochondrial permeability transition pore and cerebral ischemia-reperfusion injury in order to provide a new treatment idea for clinical treatment of cerebral ischemia-reperfusion injury.

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    Effects of Amino Acid Neurotransmitters on Nervous System and Research of Their Content Determination

    YANG Jing-han, ZHANG Zhi-chao, ZHANG Dan-shen
    ACTA NEUROPHARMACOLOGICA 2021, 11 (4): 16-. DOI:10.3969/j.issn.2095-1396.2021.04.004
    Abstract59 PDF(1078KB)( 11

    Amino acid neurotransmitters are important neurotransmitters in the brainwhich regulate the function of the human brain. Neurological diseases such as Alzheimer’s disease are closely related to amino acids in the brain. It has been widely applied at present and the amino acid content determination method has a high performance liquid chromatographyHPLCmethodthe determination of amino acid analyzer methodchromatography-mass spectrometry methodgas chromatographyetcbut these methods have certain limitationsso quick select and establish a suitable amino acids and peptides neurotransmitters efficient measurement method is particularly important. This paper reviews the methods for the determination of amino acid neurotransmitters in blood and tissue samples in recent yearsin order to provide reference for more researchers.

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    Study on Vascular Irritation of Nimodipine Injection (Ethanol-Free Type)

    SUN Ya-mei, CHENG Xiao-bo, HOU Ji-xiang, ZHANG Dan, ZHAO Bo-ce, LIN Jia-liang, LI Wei, SHEN Li-xia, WU Cui-shuan, ZHANG Qiang
    ACTA NEUROPHARMACOLOGICA 2021, 11 (4): 21-. DOI:10.3969/j.issn.2095-1396.2021.04.005
    Abstract57 PDF(5402KB)( 7

    ObjectiveThe rabbit ear-margin intravenous injection method was used to investigate the vascular irritation of nimodipine injectionethanol-free typein rabbits.MethodsThe rabbits were randomly divided into the negative control group5% glucose injection group),the nimodipine injectionethanol-free typegroupthe commercially available nimodipine injection groupand the blank preparation group. Nimodipine injections were administered through ear veins and the dosage was 0.51 mg·kg-1.The overall condition of the rabbitsthe changes in the veins and blood vessels of the ears and the surrounding tissues were observedand the ears were pathologically evaluated.ResultsThe 5% glucose injection group has no irritation to blood vessels. The vascular irritation grades of the blank preparation group and nimodipine injectionnon-ethanol typegroup are mildwhile the vascular irritation grades of animals in the commercially available nimodipine injection group are severe.ConclusionThe vascular irritation of nimodipine injectionethanol-free typeis significantly less than that of commercially available nimodipine injection. Removal of ethanol in the preparation can significantly improve the vascular irritation of nimodipine injection.

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    Advances in Pharmacokinetic Characteristics and Metabolites of Osthole

    ZHANG Zhi-chao, YANG Jing-han, ZHANG Dan-shen
    ACTA NEUROPHARMACOLOGICA 2021, 11 (4): 26-. DOI:10.3969/j.issn.2095-1396.2021.04.006
    Abstract57 PDF(1088KB)( 7

    Osthol is a natural drug component of coumarins. It is insoluble in water and has a short half-liferesulting in poor bioavailability. It is absorbed through the intestine and distributed rapidly in other tissues. This paper reviews the in vivo processpharmacokineticstargeting and metabolites of Osthol. The substances metabolized by Osthol in vivo are not the same as those simulating liver metabolism in vitro. After phasemetabolismOsthol produces demethylated ostholdehydrogenated Osthol and hydroxylated Osthol. Some studies have proved that there are no dehydrogenated products in urine and feces through in vivo metabolism detection. However other studies have shown that they can be detected in blood and urinewith lower the content of dehydrogenated products in urineand there are dehydrogenated products in liver metabolism after incubation in vitro. It is possible that dehydrogenated Osthol is an active metabolite in vivo. Clarifying the metabolic characteristics and products of Osthol in vivo and in vitro is helpful to find active metabolites.

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    Research Progress of Anti-inflammatory Activity of PPARs Agonist in the Treatment of Depression

    LIAO Yu-mei, XUE Ya-dong, CHEN Sheng, et al
    ACTA NEUROPHARMACOLOGICA 2021, 11 (2): 32-38. DOI:10.3969/j.issn.2095-1396.2021.02.007
    Abstract57 PDF(1024KB)( 3

    The occurrence of depression is usually accompanied by the appearance of inflammation. The levels of inflammatory factors such as IL-6 and TNF-αwere significantly

    increased in patients with depressionindicating that there is an important link between inflammation and the development of depression. PPARs play an important role in inhibiting inflammatory responses by interfering with NF-κBMAPKsSTAT-1activator protein 1nuclear factor of activated T cells and other signaling pathways. PPARs agonists such as WY-14643GW0742and pioglitazone have potential antidepressant effects. The research direction of PPARs as a new target for anti-inflammatory treatment of depression is the main content of this review.

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