Suppressive Effects of Neuromedin U Receptor 2-Selective Peptide Agonists on Appetite and Prolactin Secretion in Mice

内分泌学 内科学 催乳素 兴奋剂 下丘脑 食欲 多巴胺能 受体 医学 鼻腔给药 分泌物 药理学 多巴胺 激素
作者
Asuka Nomoto,Yui Suzuki,Katsuya Morito,Kazuki Nagasawa,Kentaro Takayama
出处
期刊:ACS Medicinal Chemistry Letters [American Chemical Society]
卷期号:15 (3): 376-380
标识
DOI:10.1021/acsmedchemlett.3c00541
摘要

Neuromedin U receptor 2 (NMUR2), which is expressed in the central nervous system (CNS) including the hypothalamus, has been noted as a therapeutic target against obesity. We previously reported that intranasal administration of CPN-219, a NMUR2-selective hexapeptide agonist, suppresses body weight gain in mice; however, there is no detailed information regarding its CNS effects. Recently, in addition to appetite suppression, stress responses and regulation of prolactin (PRL) secretion have also attracted attention. NMUR2 expressed in the hypothalamic tuberoinfundibular dopaminergic neurons has emerged as an alternative target for treating hyperprolactinemia. Here, CPN-219 decreased food intake up to 24 h after administration at a dose of 200 nmol, resulting in body weight gain suppression, although grooming and anxiety-like behaviors were transiently induced. Interestingly, the restraint stress-induced increase in plasma PRL levels was significantly suppressed at a lower dose of 20 nmol, indicating the potential for drug development as an anti-PRL agent of NMUR2-selective agonists.
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