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胆碱能途径参与α-常春藤苷诱导的大鼠离体胃条收缩。

Participation of cholinergic pathways in α-hederin-induced contraction of rat isolated stomach strips.

机构信息

Division of Pharmacology and Toxicology, Department of Preclinical Sciences, Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Warsaw, Poland.

出版信息

Phytomedicine. 2012 May 15;19(7):591-5. doi: 10.1016/j.phymed.2012.02.011. Epub 2012 Mar 31.

Abstract

The dry extract of Hedra helix leaves and its main active compounds, predominantly α-hederin and hederacoside C, has been traditionally believed to act spasmolytic. However, it has been recently proved that both, the extract of ivy and triterpenoid saponins, exhibit strong contractile effect on rat isolated stomach smooth muscle strips. It turned out that the most potent contractile agent isolated from the extract of ivy leaves is α-hederin. Thus, it seems reasonable to estimate the mechanism of the contractile effect of this saponin. The presented study was aimed at verifying the participation of cholinergic pathways (muscarinic and nicotine receptors) in α-hederin-induced contraction. The experiments were carried out on rat isolated stomach corpus and fundus strips under isotonic conditions. The preparations were preincubated with either atropine or hexamethonium and then exposed to α-hederin. All results are expressed as the percentage of the response to acetylcholine - a reference contractile agent. The obtained results revealed that the pretreatment of isolated stomach strips (corpus and fundus) with atropine neither prevented nor remarkably reduced the reaction of the preparations to α-hederin. Similarly, if the application of saponin was preceded by the administration of hexamethonium, the strength of the contraction of stomach fundus strips induced by α-hederin was not modified. Concluding, it can be assumed that the cholinergic pathways do not participate in α-hederin-evoked contraction of rat isolated stomach preparations.

摘要

常春藤叶的干提取物及其主要活性化合物,主要是α-常春藤苷和常春藤皂苷 C,传统上被认为具有平滑肌松弛作用。然而,最近的研究证明,常春藤提取物和三萜皂苷都对大鼠离体胃平滑肌条具有强烈的收缩作用。结果表明,从常春藤叶提取物中分离出的最有效的收缩剂是α-常春藤苷。因此,估计这种皂苷的收缩作用机制是合理的。本研究旨在验证α-常春藤苷诱导收缩过程中胆碱能途径(毒蕈碱和烟碱受体)的参与。实验在等张条件下,在大鼠离体胃体和胃底肌条上进行。将制剂用阿托品或六烃季铵预孵育,然后暴露于α-常春藤苷。所有结果均表示为乙酰胆碱(参考收缩剂)反应的百分比。结果表明,用阿托品预处理离体胃条(体和底)既不能预防也不能显著减少制剂对α-常春藤苷的反应。同样,如果在应用皂苷之前给予六烃季铵,则α-常春藤苷诱导的胃底肌条收缩强度不会改变。因此,可以假设胆碱能途径不参与α-常春藤苷引起的大鼠离体胃制剂的收缩。

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