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从文献角度看育亨宾的药理学应用。

A literature perspective on the pharmacological applications of yohimbine.

机构信息

Department of Biochemistry and Biotechnology, Centre for Research and Development, PRIST University, Vallam, Thanjavur, India.

Department of Medical Laboratory Technology, MIMS College of Allied Health Sciences, ASTER MIMS Academy, Malappuram, Kerala University of Health Sciences, Kerala, India.

出版信息

Ann Med. 2022 Dec;54(1):2861-2875. doi: 10.1080/07853890.2022.2131330.

Abstract

Phytochemicals have garnered much attention because they are useful in managing several human diseases. Yohimbine is one such phytochemical with significant pharmacological potential and could be exploited for research by medicinal chemists. It is an indole alkaloid obtained from various natural/synthetic sources. The research on yohimbine started early, and its use as a stimulant and aphrodisiac by humans has been reported for a long time. The pharmacological activity of yohimbine is mediated by the combined action of the central and peripheral nervous systems. It selectively blocks the pre and postsynaptic α-adrenergic receptors and has a moderate affinity for 1 and 2 subtypes. Yohimbine also binds to other behaviourally relevant monoaminergic receptors in the following order: α-2 NE > 5HT-1A>, 5HT-1B > 1-D > D3 > D2 receptors. The current review highlights some significant findings that contribute to developing yohimbine-based drugs. It also highlights the therapeutic potential of yohimbine against selected human diseases. However, further research is recommended on the pharmacokinetics, molecular mechanisms, and drug safety requirements using well-designed randomized clinical trials to produce yohimbine as a pharmaceutical agent for human use.Key MessagesYohimbine is a natural indole alkaloid with significant pharmacological potential.Humans have used it as a stimulant and aphrodisiac from a relatively early time.It blocks the pre- and postsynaptic α2-adrenergic receptors that could be exploited for managing erectile dysfunction, myocardial dysfunction, inflammatory disorders, and cancer.

摘要

植物化学物质因其在治疗多种人类疾病方面的作用而备受关注。育亨宾就是一种具有重要药理学潜力的植物化学物质,可能会引起药物化学家的研究兴趣。它是一种吲哚生物碱,可从天然/合成来源中获得。对育亨宾的研究很早就开始了,其作为兴奋剂和春药的用途在人类中已经有很长的历史。育亨宾的药理学活性是通过中枢和外周神经系统的共同作用介导的。它选择性地阻断前突触和后突触的 α-肾上腺素能受体,对 1 和 2 亚型具有中等亲和力。育亨宾还与其他行为相关的单胺能受体结合,其亲和力顺序如下:α2-NE > 5HT-1A > 5HT-1B > 1-D > D3 > D2 受体。本综述重点介绍了一些重要的发现,这些发现有助于开发基于育亨宾的药物。它还强调了育亨宾在治疗某些人类疾病方面的潜在治疗作用。然而,建议进行更多的研究,包括使用设计良好的随机临床试验来研究其药代动力学、分子机制和药物安全性要求,以将育亨宾开发为人类使用的药物。

关键信息

育亨宾是一种具有重要药理学潜力的天然吲哚生物碱。

人类很早就将其用作兴奋剂和春药。

它阻断前突触和后突触的 α2-肾上腺素能受体,可用于治疗勃起功能障碍、心肌功能障碍、炎症性疾病和癌症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac30/9590431/75f97cc52a66/IANN_A_2131330_F0001_B.jpg

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