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麻黄碱发现一个多世纪以来:对其药理学方面、功能和毒性与草药提取物的比较进行更新回顾。

Over a century since ephedrine discovery: an updated revisit to its pharmacological aspects, functionality and toxicity in comparison to its herbal extracts.

机构信息

Department of Biochemistry, Faculty of Pharmacy & Biotechnology, The German University in Cairo, Egypt.

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.

出版信息

Food Funct. 2021 Oct 19;12(20):9563-9582. doi: 10.1039/d1fo02093e.

Abstract

Ephedrine, a sympathomimetic amine that exhibits several adrenaline actions, is a plant alkaloid that is a common ingredient in several cold, asthma and narcolepsy treatment preparations, and in obesity management and sport medicine. Its principal action mechanism relies on its direct adrenergic actions as well as indirect role that involves the release of epinephrine and norepinephrine, thus increasing the activity of epinephrine and norepinephrine at the postsynaptic α and β receptors. Nevertheless, its serious side effects, including stroke, heart attack, drug abuse and interactions, have never been comprehensively reviewed. We conducted a systematic review of data on ephedrine, including its occurrence in functional foods, pharmacological aspects, metabolism, pharmaco/toxicokinetics and clinical features. Furthermore, a review of ephedrine natural structural analogues with regards to their differential adrenergic receptor binding affinities, food interaction, and their impact on the pharmacokinetics and effects relative to ephedrine are presented for the first time, and in comparison to its action when present in herbs.

摘要

麻黄碱是一种拟交感胺,具有多种肾上腺素能作用,是一种植物生物碱,存在于多种感冒、哮喘和嗜睡症治疗制剂中,也存在于肥胖症管理和运动医学中。其主要作用机制依赖于其直接的肾上腺素能作用以及间接的涉及肾上腺素和去甲肾上腺素释放的作用,从而增加突触后α和β受体上肾上腺素和去甲肾上腺素的活性。然而,其严重的副作用,包括中风、心脏病发作、药物滥用和相互作用,从未得到全面审查。我们对麻黄碱的数据进行了系统回顾,包括其在功能性食品中的存在、药理学方面、代谢、药物代谢动力学和临床特征。此外,我们还首次综述了麻黄碱天然结构类似物的相关内容,包括它们对肾上腺素能受体结合亲和力的差异、食物相互作用以及对药代动力学和相对于麻黄碱的作用的影响,并与它们在草药中的作用进行了比较。

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