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麦角新碱刺激人心房 5-HT-血清素受体和人心房 H-组氨酸受体。

Ergotamine Stimulates Human 5-HT-Serotonin Receptors and Human H-Histamine Receptors in the Heart.

机构信息

Institute for Pharmacology and Toxicology, Medical Faculty, Martin Luther University Halle-Wittenberg, 06120 Halle (Saale), Germany.

Institute for Pharmacology and Toxicology, Medical Faculty, Westfälische Wilhelms-Universität, 48149 Münster, Germany.

出版信息

Int J Mol Sci. 2023 Mar 1;24(5):4749. doi: 10.3390/ijms24054749.

Abstract

Ergotamine (2'-methyl-5'α-benzyl-12'-hydroxy-3',6',18-trioxoergotaman) is a tryptamine-related alkaloid from the fungus . Ergotamine is used to treat migraine. Ergotamine can bind to and activate several types of 5-HT-serotonin receptors. Based on the structural formula of ergotamine, we hypothesized that ergotamine might stimulate 5-HT-serotonin receptors or H-histamine receptors in the human heart. We observed that ergotamine exerted concentration- and time-dependent positive inotropic effects in isolated left atrial preparations in H-TG (mouse which exhibits cardiac-specific overexpression of the human H-histamine receptor). Similarly, ergotamine increased force of contraction in left atrial preparations from 5-HT-TG (mouse which exhibits cardiac-specific overexpression of the human 5-HT-serotonin receptor). An amount of 10 µM ergotamine increased the left ventricular force of contraction in isolated retrogradely perfused spontaneously beating heart preparations of both 5-HT-TG and H-TG. In the presence of the phosphodiesterase inhibitor cilostamide (1 µM), ergotamine 10 µM exerted positive inotropic effects in isolated electrically stimulated human right atrial preparations, obtained during cardiac surgery, that were attenuated by 10 µM of the H-histamine receptor antagonist cimetidine, but not by 10 µM of the 5-HT-serotonin receptor antagonist tropisetron. These data suggest that ergotamine is in principle an agonist at human 5-HT-serotonin receptors as well at human H-histamine receptors. Ergotamine acts as an agonist on H-histamine receptors in the human atrium.

摘要

麦角新碱(2'-甲基-5'α-苄基-12'-羟基-3',6',18-三氧麦角胺)是一种来自真菌的色胺相关生物碱。麦角新碱用于治疗偏头痛。麦角新碱可以与几种类型的 5-HT-血清素受体结合并激活它们。基于麦角新碱的结构公式,我们假设麦角新碱可能会刺激人类心脏中的 5-HT-血清素受体或 H-组胺受体。我们观察到,麦角新碱在 H-TG(心脏特异性过表达人类 H-组胺受体的小鼠)的分离左心房制剂中表现出浓度和时间依赖性正性肌力作用。同样,麦角新碱增加了来自 5-HT-TG(心脏特异性过表达人类 5-HT-血清素受体的小鼠)的左心房制剂的收缩力。10µM 的麦角新碱增加了两种 5-HT-TG 和 H-TG 的逆行灌注自发跳动心脏制剂的左心室收缩力。在磷酸二酯酶抑制剂西洛他唑(1µM)存在的情况下,10µM 的麦角新碱在心脏手术期间获得的分离电刺激的人类右心房制剂中表现出正性肌力作用,该作用被 10µM 的 H-组胺受体拮抗剂西咪替丁减弱,但 10µM 的 5-HT-血清素受体拮抗剂曲匹司特则没有减弱。这些数据表明,麦角新碱原则上是人类 5-HT-血清素受体以及人类 H-组胺受体的激动剂。麦角新碱在人类心房中作为 H-组胺受体的激动剂起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0ec/10003312/284b528e43c1/ijms-24-04749-g001.jpg

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