Wang Ming, Chen Qian, Li Mei, Zhou Wei, Ma Tengfei, Wang Yun, Gu Shuling
Department of Pharmacology, Xuzhou Medical College, Xuzhou, Jiangsu 221004, China.
Department of Pharmacology, Xuzhou Medical College, Xuzhou, Jiangsu 221004, China.
Peptides. 2014 Jun;56:163-72. doi: 10.1016/j.peptides.2014.04.009. Epub 2014 Apr 23.
Alarin is a newly identified member of the galanin family of peptides. Galanin has been shown to exert regulatory effects on depression. Similar to galanin in distribution, alarin is also expressed in the medial amygdala and hypothalamus, i.e., regions interrelated with depression. However, it remains a puzzle whether alarin is involved in depression. Accordingly, we established the depression-like mouse model using behavioral tests to ascertain the possible involvement of alarin, with fluoxetine as a positive control. With the positive antidepressant-like effects of alarin, we further examined its relationship to HPA axis activity and brain-derived neurotrophic factor (BDNF) levels in different brain areas in a chronic unpredictable mild stress (CUMS) paradigm. In the acute studies, alarin produced a dose-related reduction in the immobility duration in tail suspension test (TST) in mice. In the open-field test, intracerebroventricular (i.c.v.) injection of alarin (1.0 nmol) did not impair locomotion or motor coordination in the treated mice. In the CUMS paradigm, alarin administration (1.0 nmol, i.c.v.) significantly improved murine behaviors (FST and locomotor activity), which was associated with a decrease in corticotropin-releasing hormone (CRH) mRNA levels in the hypothalamus, as well as a decline in serum levels of CRH, adrenocorticotropic hormone (ACTH) and corticosterone (CORT), all of which are key hormones of the HPA axis. Furthermore, alarin upregulated BDNF mRNA levels in the prefrontal cortex and hippocampus. These findings suggest that alarin may potentiate the development of new antidepressants, which would be further secured with the identification of its receptor(s).
阿拉瑞林是新近发现的甘丙肽家族肽类成员。研究表明,甘丙肽对抑郁症具有调节作用。与甘丙肽的分布相似,阿拉瑞林也在内侧杏仁核和下丘脑表达,即与抑郁症相关的脑区。然而,阿拉瑞林是否参与抑郁症的发生仍是一个谜。因此,我们通过行为测试建立了抑郁症样小鼠模型,以确定阿拉瑞林可能的作用,氟西汀作为阳性对照。鉴于阿拉瑞林具有阳性抗抑郁样作用,我们进一步在慢性不可预测轻度应激(CUMS)模型中研究了其与不同脑区下丘脑-垂体-肾上腺(HPA)轴活性及脑源性神经营养因子(BDNF)水平的关系。在急性研究中,阿拉瑞林可使小鼠悬尾试验(TST)中的不动时间呈剂量依赖性减少。在旷场试验中,脑室内(i.c.v.)注射阿拉瑞林(1.0 nmol)对受试小鼠的运动或运动协调性无损害。在CUMS模型中,给予阿拉瑞林(1.0 nmol,i.c.v.)可显著改善小鼠行为(强迫游泳试验和运动活动),这与下丘脑促肾上腺皮质激素释放激素(CRH)mRNA水平降低以及血清中CRH、促肾上腺皮质激素(ACTH)和皮质酮(CORT)水平下降有关,这些都是HPA轴的关键激素。此外,阿拉瑞林上调了前额叶皮质和海马中的BDNF mRNA水平。这些发现表明,阿拉瑞林可能有助于开发新型抗抑郁药,随着其受体的确定,这一作用将得到进一步证实。