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草药抗抑郁药圣约翰草(贯叶连翘)对大鼠胃动力的抑制作用。

Inhibitory effect of the herbal antidepressant St. John's wort (Hypericum perforatum) on rat gastric motility.

作者信息

Capasso Raffaele, Borrelli Francesca, Aviello Gabriella, Capasso Francesco, Izzo Angelo A

机构信息

Department of Experimental Pharmacology, University of Naples Federico II, via D Montesano 49, 80131 Naples, Italy.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2008 Feb;376(6):407-14. doi: 10.1007/s00210-007-0230-2. Epub 2008 Jan 3.

Abstract

St. John's wort (Hypericum perforatum) is a highly popular and effective herbal antidepressant that clinically interacts with a number of conventional drugs. Because alterations in gastric emptying can cause pharmacokinetic interactions, in the present study we evaluated the effect of a standardized extract prepared from the flowering tops of Hypericum perforatum (SJW extract) on rat gastric motility. Orally administered SJW extract delayed gastric emptying in vivo. In vitro studies showed that SJW extract was significantly more active in inhibiting acetylcholine (or prostaglandin E2)-induced contractions than electrical field stimulation (EFS)-induced contractions. The effect of SJW extract on EFS-induced contractions was unaffected by drugs that inhibit intrinsic inhibitory nerves or by tachykinin antagonists, but it was reduced by the 5-hydroxytryptamine antagonist methysergide. The inhibitory effect of SJW extract on acetylcholine-induced contractions was reduced by the sarcoplasmic reticulum Ca2+-ATPase inhibitor cyclopiazonic acid, but not by the L-type Ca2+ channel blocker nifedipine or by methysergide. Among the chemical constituents of SJW extract tested, hyperforin and, to a lesser extent, the flavonoids kaempferol and quercitrin, inhibited acetylcholine-induced contractions. It is concluded that SJW has a direct inhibitory effect on smooth muscle and could also possibly modulate gastric neurotransmission. If extended to humans, the inhibitory effect of SJW extract on gastric emptying in vivo could contribute, at least in part, to the clinical pharmacokinetic interactions between conventional medicines and this herbal antidepressant.

摘要

圣约翰草(贯叶连翘)是一种广受欢迎且有效的草药抗抑郁剂,在临床上会与多种传统药物发生相互作用。由于胃排空的改变会导致药代动力学相互作用,因此在本研究中,我们评估了一种由贯叶连翘花顶制备的标准化提取物(圣约翰草提取物)对大鼠胃动力的影响。口服圣约翰草提取物会在体内延迟胃排空。体外研究表明,圣约翰草提取物在抑制乙酰胆碱(或前列腺素E2)诱导的收缩方面比电场刺激(EFS)诱导的收缩更具活性。圣约翰草提取物对EFS诱导收缩的作用不受抑制内在抑制神经的药物或速激肽拮抗剂的影响,但5-羟色胺拮抗剂麦角新碱会降低其作用。圣约翰草提取物对乙酰胆碱诱导收缩的抑制作用会被肌浆网Ca2 + -ATP酶抑制剂环匹阿尼酸降低,但不会被L型Ca2 +通道阻滞剂硝苯地平或麦角新碱降低。在测试的圣约翰草提取物化学成分中,金丝桃素以及程度较轻的黄酮类化合物山奈酚和槲皮苷会抑制乙酰胆碱诱导的收缩。得出的结论是,圣约翰草对平滑肌有直接抑制作用,也可能调节胃神经传递。如果推广到人类,圣约翰草提取物在体内对胃排空的抑制作用可能至少部分导致传统药物与这种草药抗抑郁剂之间的临床药代动力学相互作用。

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