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本文引用的文献

1
CORM-3 Regulates Microglia Activity, Prevents Neuronal Injury, and Improves Memory Function During Radiation-induced Brain Injury.CORM-3 调节小胶质细胞活性,预防放射性脑损伤中的神经元损伤,并改善记忆功能。
Curr Neurovasc Res. 2020;17(4):464-470. doi: 10.2174/1567202617999200730213259.
2
Ion Channel Pharmacology for Pain Modulation.用于疼痛调节的离子通道药理学
Handb Exp Pharmacol. 2019;260:161-186. doi: 10.1007/164_2019_336.
3
Heme oxygenase-1 dampens the macrophage sterile inflammasome response and regulates its components in the hypoxic lung.血红素加氧酶-1 抑制巨噬细胞无菌炎症小体反应,并调节低氧肺中的炎症小体成分。
Am J Physiol Lung Cell Mol Physiol. 2020 Jan 1;318(1):L125-L134. doi: 10.1152/ajplung.00074.2019. Epub 2019 Oct 30.
4
Levo-corydalmine Attenuates Vincristine-Induced Neuropathic Pain in Mice by Upregulating the Nrf2/HO-1/CO Pathway to Inhibit Connexin 43 Expression.左西孟旦通过上调 Nrf2/HO-1/CO 通路抑制缝隙连接蛋白 43 表达减轻长春新碱诱导的小鼠神经病理性疼痛。
Neurotherapeutics. 2020 Jan;17(1):340-355. doi: 10.1007/s13311-019-00784-7.
5
Systemic vasoprotection by inhaled carbon monoxide is mediated through prolonged alterations in monocyte/macrophage function.吸入一氧化碳的系统性血管保护作用是通过延长单核细胞/巨噬细胞功能的改变来介导的。
Nitric Oxide. 2020 Jan 1;94:36-47. doi: 10.1016/j.niox.2019.10.003. Epub 2019 Oct 5.
6
Esterase-Sensitive and pH-Controlled Carbon Monoxide Prodrugs for Treating Systemic Inflammation.酯酶敏感型和 pH 控制型一氧化碳前药治疗全身炎症。
J Med Chem. 2019 Mar 28;62(6):3163-3168. doi: 10.1021/acs.jmedchem.9b00073. Epub 2019 Mar 14.
7
Prevalence of Chronic Pain and High-Impact Chronic Pain Among Adults - United States, 2016.成年人慢性疼痛和高影响慢性疼痛的患病率 - 美国,2016 年。
MMWR Morb Mortal Wkly Rep. 2018 Sep 14;67(36):1001-1006. doi: 10.15585/mmwr.mm6736a2.
8
P2X7 Receptors Mediate CO-Induced Alterations in Gene Expression in Cultured Cortical Astrocytes-Transcriptomic Study.P2X7 受体介导 CO 诱导的皮质星形胶质细胞基因表达改变——转录组学研究。
Mol Neurobiol. 2019 May;56(5):3159-3174. doi: 10.1007/s12035-018-1302-7. Epub 2018 Aug 13.
9
Carbon monoxide protects the kidney through the central circadian clock and CD39.一氧化碳通过中央生物钟和 CD39 保护肾脏。
Proc Natl Acad Sci U S A. 2018 Mar 6;115(10):E2302-E2310. doi: 10.1073/pnas.1716747115. Epub 2018 Feb 20.
10
Neuroinflammation and Central Sensitization in Chronic and Widespread Pain.慢性广泛性疼痛中的神经炎症和中枢敏化。
Anesthesiology. 2018 Aug;129(2):343-366. doi: 10.1097/ALN.0000000000002130.

[一氧化碳与疼痛调节:综述]

[Carbon Monoxide and Pain Regulation: A Review].

作者信息

Zheng Zhi-Yao, Jin Yu-Ming, Jin Si-Yi, Ke Bo-Wen

机构信息

West China School of Medicine, Sichuan University, Chengdu 610041, China.

Laboratory of Anesthesiology & Critical Care Medicine, Translational Neuroscience Center, West China Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2021 May;52(3):396-401. doi: 10.12182/20210560102.

DOI:10.12182/20210560102
PMID:34018356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10409187/
Abstract

Carbon monoxide (CO) is an endogenous gasotransmitter produced by the degradation of heme in the presence of heme oxygenase (HO) in mammals. It has been demonstrated that CO participates in a variety of physiological activities and pathological processes, and is closely related to cell protection and homeostasis maintenance in organ tissues. It has been shown by a growing number of studies that CO may play a regulatory and interventional role in the process of the occurrence and development of pain through a variety of mechanisms of action. However, its mechanism of action is still not fully understood and the uncontrollable factors concerning CO administration also placed considerable limitation to its application. This paper reviews the potential targets and pathways of CO in pain regulation and discusses the challenges and opportunities in the clinical application of CO in order to provide suggestions for further exploration and development of CO analgesics.

摘要

一氧化碳(CO)是哺乳动物体内在血红素加氧酶(HO)存在的情况下由血红素降解产生的一种内源性气体递质。已经证明,CO参与多种生理活动和病理过程,并且与器官组织中的细胞保护和内环境稳态维持密切相关。越来越多的研究表明,CO可能通过多种作用机制在疼痛的发生和发展过程中发挥调节和干预作用。然而,其作用机制仍未完全了解,并且与CO给药相关的不可控因素也对其应用造成了相当大的限制。本文综述了CO在疼痛调节中的潜在靶点和途径,并讨论了CO临床应用中的挑战和机遇,以便为进一步探索和开发CO镇痛药提供建议。