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J Zhejiang Univ Sci B. 2020;21(3):204-217. doi: 10.1631/jzus.B1900425.
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1
MicroRNAs in tumor immunity: functional regulation in tumor-associated macrophages.肿瘤免疫中的 microRNAs:肿瘤相关巨噬细胞中的功能调控。
J Zhejiang Univ Sci B. 2020;21(1):12-28. doi: 10.1631/jzus.B1900452.
2
Circular RNA expression profile in the spinal cord of morphine tolerated rats and screen of putative key circRNAs.吗啡耐受大鼠脊髓中环状 RNA 的表达谱及潜在关键环状 RNA 的筛选
Mol Brain. 2019 Sep 18;12(1):79. doi: 10.1186/s13041-019-0498-4.
3
Acute antinociceptive effect of fish oil or its major compounds, eicosapentaenoic and docosahexaenoic acids on diabetic neuropathic pain depends on opioid system activation.鱼油或其主要成分二十碳五烯酸和二十二碳六烯酸对糖尿病性神经痛的急性镇痛作用依赖于阿片系统的激活。
Behav Brain Res. 2019 Oct 17;372:111992. doi: 10.1016/j.bbr.2019.111992. Epub 2019 May 30.
4
MicroRNAs in Microglia: How do MicroRNAs Affect Activation, Inflammation, Polarization of Microglia and Mediate the Interaction Between Microglia and Glioma?小胶质细胞中的微小RNA:微小RNA如何影响小胶质细胞的激活、炎症反应、极化并介导小胶质细胞与胶质瘤之间的相互作用?
Front Mol Neurosci. 2019 May 10;12:125. doi: 10.3389/fnmol.2019.00125. eCollection 2019.
5
Activation of spinal Extacellular Signal-Regulated Kinases and c-jun N-terminal kinase signaling pathways contributes to morphine-induced acute and chronic hyperalgesia in mice.脊髓细胞外信号调节激酶和 c-jun N-末端激酶信号通路的激活导致小鼠吗啡诱导的急性和慢性痛觉过敏。
J Cell Biochem. 2019 Sep;120(9):15045-15056. doi: 10.1002/jcb.28766. Epub 2019 Apr 23.
6
Chemokines CCL2 and CCL7, but not CCL12, play a significant role in the development of pain-related behavior and opioid-induced analgesia.趋化因子 CCL2 和 CCL7,但不是 CCL12,在疼痛相关行为和阿片类药物诱导的镇痛的发展中起着重要作用。
Cytokine. 2019 Jul;119:202-213. doi: 10.1016/j.cyto.2019.03.007. Epub 2019 Apr 16.
7
Inhibition of apoptosis signal-regulating kinase by paeoniflorin attenuates neuroinflammation and ameliorates neuropathic pain.芍药苷通过抑制凋亡信号调节激酶减轻神经炎症并改善神经病理性疼痛。
J Neuroinflammation. 2019 Apr 11;16(1):83. doi: 10.1186/s12974-019-1476-6.
8
Morphine increases macrophages at the lesion site following spinal cord injury: Protective effects of minocycline.脊髓损伤后吗啡增加病变部位的巨噬细胞:米诺环素的保护作用。
Brain Behav Immun. 2019 Jul;79:125-138. doi: 10.1016/j.bbi.2019.01.023. Epub 2019 Jan 23.
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Cathepsin C promotes microglia M1 polarization and aggravates neuroinflammation via activation of Ca-dependent PKC/p38MAPK/NF-κB pathway.组织蛋白酶 C 通过激活 Ca2+ 依赖性 PKC/p38MAPK/NF-κB 通路促进小胶质细胞 M1 极化并加重神经炎症。
J Neuroinflammation. 2019 Jan 16;16(1):10. doi: 10.1186/s12974-019-1398-3.
10
The Effects of Minocycline on the Hippocampus in Lithium- Pilocarpine Induced Status Epilepticus in Rat: Relations with Microglial/Astrocytic Activation and Serum S100B Level.米诺环素对锂-匹罗卡品诱导的大鼠癫痫持续状态海马的影响:与小胶质细胞/星形胶质细胞激活及血清S100B水平的关系
Turk Neurosurg. 2019;29(1):95-105. doi: 10.5137/1019-5149.JTN.22744-18.1.

小胶质细胞抑制剂在神经病理性疼痛和吗啡耐受中的调控机制及治疗潜力。

Regulatory mechanisms and therapeutic potential of microglial inhibitors in neuropathic pain and morphine tolerance.

机构信息

Department of Physiology, Basic Medical College of Nanchang University, Nanchang 330006, China.

Department of Fourth Clinical Medicine, School of Medicine, Nanchang University, Nanchang 330006, China.

出版信息

J Zhejiang Univ Sci B. 2020;21(3):204-217. doi: 10.1631/jzus.B1900425.

DOI:10.1631/jzus.B1900425
PMID:32133798
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7086010/
Abstract

Microglia are important cells involved in the regulation of neuropathic pain (NPP) and morphine tolerance. Information on their plasticity and polarity has been elucidated after determining their physiological structure, but there is still much to learn about the role of this type of cell in NPP and morphine tolerance. Microglia mediate multiple functions in health and disease by controlling damage in the central nervous system (CNS) and endogenous immune responses to disease. Microglial activation can result in altered opioid system activity, and NPP is characterized by resistance to morphine. Here we investigate the regulatory mechanisms of microglia and review the potential of microglial inhibitors for modulating NPP and morphine tolerance. Targeted inhibition of glial activation is a clinically promising approach to the treatment of NPP and the prevention of morphine tolerance. Finally, we suggest directions for future research on microglial inhibitors.

摘要

小胶质细胞是参与神经病理性疼痛(NPP)和吗啡耐受调节的重要细胞。在确定其生理结构后,阐明了它们的可塑性和极性信息,但对于这种细胞在 NPP 和吗啡耐受中的作用,仍有许多需要了解。小胶质细胞通过控制中枢神经系统(CNS)的损伤和对疾病的内源性免疫反应来介导多种健康和疾病中的功能。小胶质细胞的激活可导致阿片系统活性改变,NPP 的特征是对吗啡的耐药性。在这里,我们研究了小胶质细胞的调节机制,并综述了小胶质细胞抑制剂调节 NPP 和吗啡耐受的潜力。靶向抑制神经胶质细胞的激活是治疗 NPP 和预防吗啡耐受的一种很有前途的临床方法。最后,我们为小胶质细胞抑制剂的未来研究提出了方向。