Melanin-concentrating hormone MCH1 receptor antagonists -: A potential new approach to the treatment of depression and anxiety disorders

被引:62
作者
Shimazaki, Toshiharu [1 ]
Yoshimizu, Takao [1 ]
Chaki, Shigeyuki [1 ]
机构
[1] Taisho Pharmaceut Co Ltd, Med Res Labs, Med Pharmacol Lab, Kita Ku, Saitama, Saitama 3319530, Japan
关键词
D O I
10.2165/00023210-200620100-00002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Melanin-concentrating hormone (MCH) is a cyclic 19-amino-acid neuropeptide that has been considered to play a key role in the regulation of feeding and energy homeostasis. To date, two receptor subtypes for MCH (designated MCH1 and MCH2) have been identified; the MCH1 receptor has been proposed to mediate the physiological functions of MCH in rodents. In addition to the crucial roles of MCH in feeding behaviour, anatomical and neurochemical studies suggest that the MCH/MCH1 system is involved in the regulation of emotion and stress responses. This assumption has been supported by a recent series of neurochemical and behavioural studies. Indeed, several lines of evidence show that MCH activates stress responses and induces depressive- and anxiety-like behaviours, while the blockade of MCH1 receptors results in antidepressant and anxiolytic effects in various rodent models. Moreover, MCH may decrease reward activity while increasing hypothalamus-pituitary adrenal axis activity, both of which may underlie the neurochemical mechanisms of the depression and anxiety-like effects induced by MCH. The effects of MCH1 receptor antagonists in animal models, together with their rapid onset of effect and lack of adverse CNS effects, suggest that they deserve further investigation as potential new treatments for depression and anxiety disorders.
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页码:801 / 811
页数:11
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