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从鸡矢藤(Paederia scandens(Lour.)Merrill.)中分离得到的鸡矢藤酸在小鼠和大鼠中的抗惊厥和镇静作用。

Anticonvulsant and sedative effects of paederosidic acid isolated from Paederia scandens (Lour.) Merrill. in mice and rats.

机构信息

Department of Neurosurgery, Chengdu Military General Hospital, Chengdu 610083, PR China; Third Military Medical University, Chongqing 400038, PR China.

出版信息

Pharmacol Biochem Behav. 2013 Oct;111:97-101. doi: 10.1016/j.pbb.2013.08.015. Epub 2013 Sep 9.

Abstract

This study was designed to evaluate the anticonvulsant and sedative effects of paederosidic acid isolated from Paederia scandens (Lour.) Merrill. in mice and rats. In the present study, anticonvulsant activities of paederosidic acid were evaluated by maximal electroshock and pentylenetetrazole-induced seizures in male mice. Then, pentobarbital sodium-induced sleeping time and locomotor activity tests in mice were used to evaluate the sedative effects of paederosidic acid. Finally, the mechanism of paederosidic acid was explored by evaluating the contents of Glu and GABA in the brain, and Western blot was used to measure GAD65 expression in the mouse brain. Paederosidic acid (5, 10, 20, and 40 mg/kg, ip) had significant anticonvulsant and sedative effects. Moreover, paederosidic acid increased brain gamma-aminobutyric acid and decreased glutamic acid in the brain, and it up-regulated expressions of GAD 65. In conclusion, our results suggest that paederosidic acid may be a promising future therapeutic agent for treatment of epilepsy.

摘要

本研究旨在评估从鸡矢藤(Paederia scandens(Lour.)Merrill.)中分离得到的鸡矢藤酸的抗惊厥和镇静作用。在本研究中,通过最大电休克和戊四氮诱导的雄性小鼠癫痫发作来评估鸡矢藤酸的抗惊厥活性。然后,通过戊巴比妥钠诱导的睡眠时间和小鼠运动活性试验来评估鸡矢藤酸的镇静作用。最后,通过评估脑内 Glu 和 GABA 的含量,以及通过 Western blot 测量小鼠脑内 GAD65 的表达,来探讨鸡矢藤酸的作用机制。鸡矢藤酸(5、10、20 和 40 mg/kg,ip)具有显著的抗惊厥和镇静作用。此外,鸡矢藤酸增加了脑内γ-氨基丁酸并降低了脑内谷氨酸水平,同时上调了 GAD65 的表达。综上所述,我们的研究结果表明,鸡矢藤酸可能是一种有前途的治疗癫痫的潜在药物。

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