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山莨菪碱在休克中的有益作用涉及胆碱能抗炎途径。

Beneficial effects of anisodamine in shock involved cholinergic anti-inflammatory pathway.

作者信息

Zhao Ting, Li Dong-Jie, Liu Chong, Su Ding-Feng, Shen Fu-Ming

机构信息

Department of Pharmacology, School of Pharmacy, Second Military Medical University Shanghai, China.

出版信息

Front Pharmacol. 2011 May 2;2:23. doi: 10.3389/fphar.2011.00023. eCollection 2011.

Abstract

Anisodamine, an antagonist of muscarinic receptor, has been used therapeutically to improve blood flow in circulatory disorders such as septic shock in China since 1965. The main mechanism of anisodamine for anti-shock proposed in Pharmacology for Chinese medical students is to improve blood flow in the microcirculation. Here, we suggest a new mechanism for its anti-shock effect. That is, anisodamine, by blocking muscarinic receptor, results in rerouting of acetylcholine to α7 nicotinic acetylcholine receptor (α7nAChR) bringing about increased acetylcholine-mediated activation of α7nAChR and the cholinergic anti-inflammatory pathway.

摘要

山莨菪碱是一种毒蕈碱受体拮抗剂,自1965年以来在中国已被用于治疗改善循环障碍(如感染性休克)中的血流。中国医学生药理学中提出的山莨菪碱抗休克的主要机制是改善微循环中的血流。在此,我们提出了其抗休克作用的一种新机制。即山莨菪碱通过阻断毒蕈碱受体,导致乙酰胆碱重新导向α7烟碱型乙酰胆碱受体(α7nAChR),从而增加乙酰胆碱介导的α7nAChR激活和胆碱能抗炎途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6f/3108475/fd14bb687f7a/fphar-02-00023-g001.jpg

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