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来自红海软珊瑚金色肉芝软珊瑚的抗癫痫神经酰胺的作用机制。

Mechanism of action of antiepileptic ceramide from Red Sea soft coral Sarcophyton auritum.

作者信息

Eltahawy Nermeen A, Ibrahim Amany K, Radwan Mohamed M, Zaitone Sawsan A, Gomaa Mohamed, ElSohly Mahmoud A, Hassanean Hashim A, Ahmed Safwat A

机构信息

Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt

出版信息

Bioorg Med Chem Lett. 2015 Dec 15;25(24):5819-24. doi: 10.1016/j.bmcl.2015.08.039.

Abstract

Chemical investigation of the Red Sea soft coral Sarcophyton auritum led to the isolation and structure elucidation of a new ceramide N-((2S,3R,4E,6E)-1,3-dihydroxyhenicosa-4,6-dien-2-yl)tridecanamide (1). Structure elucidation was achieved using spectroscopic techniques, including 1D and 2D NMR and HRMS. The anticonvulsant activity of the isolated ceramide was measured in vivo using the pentylenetetrazole (PTZ)-induced seizure model, where it successfully antagonized the lethality of pentylenetetrazole in mice. In addition, the isolated ceramide showed good anxiolytic activity when used in the light–dark transition box and the elevated plus maze compared to diazepam. The molecular modeling studies for the antiepileptic and antianxiety mechanism of the isolated ceramide suggested a CNS depressing activity possibly through GABA and serotonin receptors modulation. The pharmacological activity of the ceramide involved agonistic activity on GABA-A receptors but not 5HT3 receptors.

摘要

对红海软珊瑚金色肉芝软珊瑚进行化学研究,导致分离并阐明了一种新的神经酰胺N - ((2S,3R,4E,6E)-1,3 - 二羟基二十一碳 - 4,6 - 二烯 - 2 - 基)十三烷酰胺(1)的结构。使用包括一维和二维核磁共振以及高分辨率质谱在内的光谱技术实现了结构阐明。使用戊四氮(PTZ)诱导的癫痫模型在体内测量了分离出的神经酰胺的抗惊厥活性,在该模型中它成功拮抗了戊四氮对小鼠的致死性。此外,与地西泮相比,分离出的神经酰胺在明暗转换箱和高架十字迷宫中使用时显示出良好的抗焦虑活性。对分离出的神经酰胺的抗癫痫和抗焦虑机制的分子建模研究表明,其可能通过调节γ-氨基丁酸(GABA)和5-羟色胺受体而具有中枢神经系统抑制活性。该神经酰胺的药理活性涉及对GABA - A受体的激动活性,但对5HT3受体无此活性。

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