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金雀花碱,一种α4β2烟碱型乙酰胆碱受体的部分激动剂,可减轻不可预测的慢性轻度应激诱导的抑郁样行为。

Cytisine, a Partial Agonist of α4β2 Nicotinic Acetylcholine Receptors, Reduced Unpredictable Chronic Mild Stress-Induced Depression-Like Behaviors.

作者信息

Han Jing, Wang Dong-Sheng, Liu Shui-Bing, Zhao Ming-Gao

机构信息

Department of Pharmacology, School of Pharmacy, The Fourth Military Medical University, Xi'an 710032, China.

Department of Orthopedics, Jinling Hospital, Clinical School of Nanjing, Second Military Medical University, Nanjing 210002, China.

出版信息

Biomol Ther (Seoul). 2016 May 1;24(3):291-7. doi: 10.4062/biomolther.2015.113.

Abstract

Cytisine (CYT), a partial agonist of α4β2-nicotinic receptors, has been used for antidepressant efficacy in several tests. Nicotinic receptors have been shown to be closely associated with depression. However, little is known about the effects of CYT on the depression. In the present study, a mouse model of depression, the unpredictable chronic mild stress (UCMS), was used to evaluate the activities of CYT. UCMS caused significant depression-like behaviors, as shown by the decrease of total distances in open field test, and the prolonged duration of immobility in tail suspension test and forced swimming test. Treatment with CYT for two weeks notably relieved the depression-like behaviors in the UCMS mice. Next, proteins related to depressive disorder in the brain region of hippocampus and amygdala were analyzed to elucidate the underlying mechanisms of CYT. CYT significantly reversed the decreases of 5-HT1A, BDNF, and mTOR levels in the hippocampus and amygdala. These results imply that CYT may act as a potential anti-depressant in the animals under chronic stress.

摘要

金雀花碱(CYT)是α4β2-烟碱型受体的部分激动剂,已在多项试验中用于评估其抗抑郁疗效。烟碱型受体已被证明与抑郁症密切相关。然而,关于CYT对抑郁症的影响知之甚少。在本研究中,使用一种抑郁症小鼠模型——不可预测的慢性轻度应激(UCMS)来评估CYT的活性。UCMS导致了显著的抑郁样行为,如旷场试验中总移动距离减少,以及悬尾试验和强迫游泳试验中不动时间延长。用CYT治疗两周显著缓解了UCMS小鼠的抑郁样行为。接下来,分析海马体和杏仁核脑区中与抑郁症相关的蛋白质,以阐明CYT的潜在作用机制。CYT显著逆转了海马体和杏仁核中5-HT1A、脑源性神经营养因子(BDNF)和雷帕霉素靶蛋白(mTOR)水平的降低。这些结果表明,CYT可能是慢性应激动物潜在的抗抑郁剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97e6/4859792/2952ef50e984/bt-24-291f1.jpg

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