植物多酚对抑郁症中枢神经炎症干预机制的研究进展
  • ISSN:3135-7571(Print) 3135-758X(Online)
  • DOI:
  • 出版频率:月刊
  • 语言:中文
  • 收录数据库:Crossref

植物多酚对抑郁症中枢神经炎症干预机制的研究进展

郭钰婷 龚思 张 航 李 敏 杨 彦

1.成都中医药大学养生康复学院,四川 成都 610075 2.成都中医药大学第三附属医院,四川 成都 610041

摘要:摘要:神经炎症是中枢神经系统中各种促炎细胞因子和抗炎细胞因子合成及释放失调,从而引起的炎症反应。现越来越多的证据表明中枢神经炎症参与抑郁症的病理生理。现临床应用的抗抑郁药物多存在抗抑郁谱窄、不良反应大、易复发等缺点,这促使研究人员从植物中寻找天然、高效、低毒的天然抗抑郁药。多酚是一种具有抗氧化和抗炎特性的广泛化合物,其可能是治疗炎症相关抑郁症等神经精神症状的一种有前途和有效的辅助疗法。本文基于神经炎症通路总结了植物多酚提取物对改善抑郁症患者症状的临床证据及其可能作用机制,为植物多酚的临床应用提供理论依据。

关键词:关键词: 多酚;抑郁症;神经炎症; 防治机制;综述

参考文献:

[1] HUANG Y, WANG Y, WANG H, et al. Prevalence ofmental disorders in China: a cross-sectional epidemiological study [J]. Lancet Psychiatry, 2019, 6(3): 211-224.

[2] MARX W, LANE M, HOCKEY M, et al. Diet and depression: exploring the biological mechanisms of action [J]. Mol Psychiatry, 2021, 26(1):

134-150.

[3] LEE D H, LEE J Y, HONG D Y, et al.

Pharmacological Treatment for Neuroinflammation in Stress-Related Disorder [J]. Biomedicines, 2022, 10(10).

[4] PETRALIA M C, MAZZON E, FAGONE P, et al. The cytokine network in the pathogenesis of major depressive disorder. Close to translation? [J]. Autoimmunity Reviews, 2020, 19(5): 15.

[5] DONOSO F, EGERTON S, BASTIAANSSEN T F S, et al. Polyphenols selectively reverse early-life stress-induced behavioural, neurochemical and microbiota changes in the rat [J].

Psychoneuroendocrinology, 2020, 116: 104673.

[6] ROMAN M, IRWIN M R. Novel neuroimmunologic therapeutics in depression: A clinical

perspective on what we know so far [J]. Brain Behavior and Immunity, 2020, 83: 7-21.

[7] ERJAVEC G N, SAGUD M, PERKOVIC M N, et al. Depression: Biological markers and treatment [J]. Progress in Neuro-Psychopharmacology &

Biological Psychiatry, 2021, 105: 19.

[8] HERMAN F J, PASINETTI G M. Principles of

inflammasome priming and inhibition:

Implications for psychiatric disorders [J]. Brain Behav Immun, 2018, 73: 66-84.

[9] RICHARDS E M, ZANOTTI-FREGONARA P, FUJITA M, et al. PET radioligand binding to translocator protein (TSPO) is increased in unmedicated

depressed subjects [J]. Ejnmmi Research, 2018, 8: 9.

[10] LI H, SAGAR A P, KERI S. Translocator protein (18 kDa TSPO) binding, a marker of microglia, is reduced in major depression during

cognitive-behavioral therapy [J]. Progress in

Neuro-Psychopharmacology & Biological Psychiatry 2018, 83: 1-7.

[11] 万腾, 高雪, 刘顺峰, et al. 小胶质细胞极化与抑郁症关系的研究进展(英文) [J]. 生物化学与生物物理进展, 2021, 48(12): 1404-1413.

[12] BORIERO D, CARCERERI DE PRATI A, ANTONINI L, et al. The anti-STAT1 polyphenol myricetin

inhibits M1 microglia activation and counteracts neuronal death [J]. Febs j, 2021, 288(7):

2347-2359.

[13] GU X H, XU L J, ZHENG L L, et al. Long

non-coding RNA uc.80- overexpression promotes M2 polarization of microglias to ameliorate

depression in rats [J]. IUBMB Life, 2020, 72(10): 2194-2203.

[14] LI M X, ZHENG H L, LUO Y, et al. Gene

deficiency and pharmacological inhibition of

caspase-1 confers resilience to chronic social defeat stress via regulating the stability of surface AMPARs [J]. Molecular Psychiatry, 2018, 23(3): 556-568.

[15] INSERRA A, MASTRONARDI C A, ROGERS G, et al. Neuroimmunomodulation in Major Depressive

Disorder: Focus on Caspase 1, Inducible Nitric Oxide Synthase, and Interferon-Gamma [J]. Mol Neurobiol, 2019, 56(6): 4288-4305.

[16] LI Z, HUANG Z, ZHANG H, et al. P2X7 Receptor Induces Pyroptotic Inflammation and Cartilage Degradation in Osteoarthritis via NF-κB/NLRP3 Crosstalk [J]. Oxid Med Cell Longev, 2021, 2021: 8868361.

[17] IWATA M, OTA K T, LI X Y, et al. Psychological Stress Activates the Inflammasome via Release of Adenosine Triphosphate and Stimulation of the Purinergic Type 2X7 Receptor [J]. Biol Psychiatry 2016, 80(1): 12-22.

[18] LIU L R, LIU J C, BAO J S, et al. Interaction of Microglia and Astrocytes in the Neurovascular Unit [J]. Front Immunol, 2020, 11: 1024.

[19] TALIFU Z, LIU J Y, PAN Y Z, et al. In vivo astrocyte-to-neuron reprogramming for centralnervous system regeneration: a narrative review [J]. Neural Regen Res, 2023, 18(4): 750-755.

[20] TAMARU T, KOBAYAKAWA K, SAIWAI H, et al. Glial scar survives until the chronic phase by

recruiting scar-forming astrocytes after spinal cord injury [J]. Exp Neurol, 2023, 359: 114264.

[21] KWON H S, KOH S H. Neuroinflammation in

neurodegenerative disorders: the roles of

microglia and astrocytes [J]. Transl Neurodegener, 2020, 9(1): 42.

[22] MARINA N, CHRISTIE I N, KORSAK A, et al. Astrocytes monitor cerebral perfusion and control systemic circulation to maintain brain blood flow [J]. Nat Commun, 2020, 11(1): 131.

[23] 何沙潼, 蒋梦若, 陈嘉豪, et al. 抑郁的中枢神经炎症机制相关研究进展 [J]. 生命的化学, 2022, 42(07): 1315-1321.

[24] CHENG T, XU Z, MA X. The role of astrocytes in neuropathic pain [J]. Front Mol Neurosci, 2022, 15: 1007889.

[25] WOHLEB E S, FRANKLIN T, IWATA M, et al.

Integrating neuroimmune systems in the

neurobiology of depression [J]. Nat Rev Neurosci, 2016, 17(8): 497-511.

[26] HAN M, YUAN L, HUANG Y, et al. Integrated co-expression network analysis uncovers novel tissue-specific genes in major depressive

disorder and bipolar disorder [J]. Front Psychiatry, 2022, 13: 980315.

[27] PRICE R B, DUMAN R. Neuroplasticity in cognitive and psychological mechanisms of

depression: an integrative model [J]. Mol Psychiatry, 2020, 25(3): 530-543.

[28] PLANCHEZ B, SURGET A, BELZUNG C. Adult

hippocampal neurogenesis and antidepressants

effects [J]. Curr Opin Pharmacol, 2020, 50: 88-95.

[29] DURAZZO A, LUCARINI M, SOUTO E B, et al. Polyphenols: A concise overview on the chemistry, occurrence, and human health [J]. Phytother Res, 2019, 33(9): 2221-2243.

[30] OFOSU F K, DALIRI E B M, ELAHI F, et al. New

Insights on the Use of Polyphenol s as Natural Preservatives and Their Emerging Safety Concerns [J]. Frontiers in Sustainable Food Systems, 2020, 4: 14.