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茵陈蒿水提物通过钙通道阻断和抗胆碱能途径的肌松和抗痉挛作用。

Myorelaxant and antispasmodic effect of an aqueous extract of Artemisia campestris L. via calcium channel blocking and anticholinergic pathways.

机构信息

Laboratory of Bioresources, Biotechnology, Ethnopharmacology and Health, Department of Biology, Faculty of Sciences, Mohamed the First University, Boulevard Mohamed VI; BP: 717; 60000, Oujda, Morocco.

出版信息

J Smooth Muscle Res. 2021;57(0):35-48. doi: 10.1540/jsmr.57.35.

Abstract

Intestinal spasms are violent contractions that occur in the intestine, which cause discomfort to people who have them. Medicinal plants are widely used in traditional Moroccan medicine to treat these problems, among these being Artemisia campestris L. This study aims to evaluate the relaxant and antispasmodic effects of an aqueous extract of this plant (ACAE). It was performed in vitro on isolated segments of both isolated rat and rabbit jejunum mounted in an organ bath and tension recordings made via an isotonic transducer. ACAE caused a myorelaxant effect on baseline rabbit jejunum contractions in a dose-dependent and reversible manner with an IC of 1.52 ± 0.12 mg/ml. This extract would not act via adrenergic receptors pathway. On the other hand, the extract caused a dose-dependent relaxation of the jejunum tone in rat jejenum segments pre-contracted with either Carbachol (CCh; 10 M) or high K (KCl 75 mM) with an IC = 0.49 ± 0.02 mg/ml and 0.36 ± 0.02 mg/ml respectively. In the presence of different doses of the extract, the maximum response to CCh and CaCl was significantly reduced. This demonstrates that ACAE acts on both muscarinic receptors and voltage-dependent calcium channels. Thus, the plant extract acted on both muscarinic and nicotinic receptors and acts on the guanylate cyclase pathway, but not the nitric oxide pathway. These results indicate the mechanism by which Artemisia campestris L. acts as an effective antispasmodic agent in traditional Moroccan medicine.

摘要

肠痉挛是发生在肠道中的剧烈收缩,会给患者带来不适。药用植物在摩洛哥传统医学中被广泛用于治疗这些问题,其中包括 Artemisia campestris L. 本研究旨在评估该植物(ACAE)的水提物的松弛和抗痉挛作用。在离体大鼠和兔空肠段上进行体外实验,将其安装在器官浴中,并通过等张换能器进行张力记录。ACAE 以剂量依赖和可恢复的方式对兔空肠基础收缩产生了肌松作用,IC 为 1.52±0.12mg/ml。这种提取物不会通过肾上腺素能受体途径起作用。另一方面,提取物对预先用 Carbachol(CCh;10μM)或高 K(KCl 75mM)收缩的大鼠空肠段的肠张力产生剂量依赖性松弛,IC 分别为 0.49±0.02mg/ml 和 0.36±0.02mg/ml。在存在不同剂量的提取物的情况下,对 CCh 和 CaCl 的最大反应明显降低。这表明 ACAE 作用于毒蕈碱受体和电压依赖性钙通道。因此,植物提取物作用于毒蕈碱和烟碱受体,并作用于鸟苷酸环化酶途径,而不是一氧化氮途径。这些结果表明了 Artemisia campestris L. 作为摩洛哥传统医学中有效抗痉挛药物的作用机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7ca/8443802/1c8b683ffb0d/jsmr-57-035-g001.jpg

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