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逍遥散加味方(FEWP)通过刺激别孕烯醇酮的生物合成改善创伤后应激障碍动物模型的行为缺陷。

Free and Easy Wanderer Plus (FEWP) improves behavioral deficits in an animal model of post-traumatic stress disorder by stimulating allopregnanolone biosynthesis.

作者信息

Qiu Zhi-Kun, Zhang Guan-Hua, He Jia-Li, Ma Jian-Chun, Zeng Jia, Shen Dong, Shen Yong-Gang, Chen Ji-Sheng, Liu Cheng-Yong

机构信息

Pharmaceutical Department of the First Affiliated Hospital of Guangdong Pharmaceutical University, Clinical Pharmacy Department of Guangdong Pharmaceutical University, Guangzhou 510080, PR China.

Neurosurgery Department of the Third Affiliated Hospital of Southern Medical University, Guangzhou 510630, PR China.

出版信息

Neurosci Lett. 2015 Aug 18;602:162-6. doi: 10.1016/j.neulet.2015.06.055. Epub 2015 Jul 6.

Abstract

Post-traumatic stress disorder (PTSD) is a severe psychiatric condition defined as a "trauma and stress-related disorder". Dampened allopregnanolone biosynthesis has been implicated as a possible contributor to PTSD aetiology. Free and Easy Wanderer Plus (FEWP) is a traditional Chinese medicine previously shown to be effective in PTSD treatment. However, little is known about the role of allopregnanolone in the anti-PTSD effects of FEWP. To evaluate this, the single prolonged stress (SPS) model was used in the present study. SPS-induced rats were administered FEWP (at doses of 2.5, 5.0 and 10.0 mg/kg, p.o.) after induction of SPS from days 2 through 15. After exposure to SPS, behavioral assessments were determined, including the open-field test, the contextual fear paradigm, and the elevated plus-maze test. The experimental model rats were decapitated at the end of the behavioral tests and the level of allopregnanolone in the prefrontal cortex, hippocampus and amygdala was measured by enzyme linked immunosorbent assay (ELISA). The behavioral deficits of the SPS-induced rats were significantly reversed by FEWP (at doses of 5.0 and 10.0 mg/kg, p.o.). The level of allopregnanolone was increased by administration of FEWP. In summary, this study indicated that the anti-PTSD effects of FEWP were associated with allopregnanolone biosynthesis.

摘要

创伤后应激障碍(PTSD)是一种严重的精神疾病,被定义为“创伤及应激相关障碍”。孕烷醇酮生物合成受抑制被认为可能是PTSD病因的一个促成因素。逍遥散加味(FEWP)是一种传统中药,先前已证明其对PTSD治疗有效。然而,关于孕烷醇酮在FEWP抗PTSD作用中的作用知之甚少。为评估这一点,本研究采用了单次延长应激(SPS)模型。在第2天至第15天诱导SPS后,对SPS诱导的大鼠口服给予FEWP(剂量分别为2.5、5.0和10.0 mg/kg)。暴露于SPS后,进行行为评估,包括旷场试验、情境恐惧范式和高架十字迷宫试验。行为测试结束时,将实验模型大鼠断头,通过酶联免疫吸附测定(ELISA)测量前额叶皮质、海马体和杏仁核中孕烷醇酮的水平。FEWP(剂量为5.0和10.0 mg/kg,口服)显著逆转了SPS诱导大鼠的行为缺陷。给予FEWP可提高孕烷醇酮水平。总之,本研究表明FEWP的抗PTSD作用与孕烷醇酮生物合成有关。

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