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

Q3 Medicine
Mohamed Marghich, Ouafa Amrani, Hassane Mekhfi, Abderrahim Ziyyat, Mohamed Bnouham, Mohammed Aziz
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引用次数: 4

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 IC50 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; 10-6 M) or high K+ (KCl 75 mM) with an IC50 = 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 CaCl2 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.

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青蒿水提物通过钙通道阻断和抗胆碱能通路的肌肉松弛和抗痉挛作用。
肠痉挛是发生在肠道内的剧烈收缩,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,其中包括青蒿(Artemisia campestris L.)。本研究旨在评估该植物水提取物(ACAE)的松弛和抗痉挛作用。在离体大鼠和家兔空肠的分离段上进行体外实验,并通过等渗换能器记录张力。ACAE对兔空肠收缩基线产生肌松弛作用,其IC50为1.52±0.12 mg/ml,呈剂量依赖性和可逆性。该提取物不通过肾上腺素能受体途径起作用。另一方面,该提取物引起大鼠空肠节段空肠张力的剂量依赖性松弛,这些空肠节段与Carbachol (CCh;10-6 M)或高K+ (KCl 75 mM), IC50分别为0.49±0.02 mg/ml和0.36±0.02 mg/ml。在不同剂量的提取物存在下,对CCh和CaCl2的最大反应显着降低。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,但不作用于一氧化氮途径。这些结果提示了在摩洛哥传统医学中,campestris L.作为一种有效的抗痉挛药的机制。
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来源期刊
Journal of Smooth Muscle Research
Journal of Smooth Muscle Research Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
2.30
自引率
0.00%
发文量
7
审稿时长
10 weeks
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