Pharmacological comparison of rat and human melanocortin 3 and 4 receptors in vitro

被引:30
作者
Schiöth, HB
Bouifrouri, AA
Rudzish, R
Muceniece, R
Watanobe, H
Wikberg, JES
Larhammar, D
机构
[1] Uppsala Univ, Biomed Ctr, Dept Neurosci, S-75124 Uppsala, Sweden
[2] Latvian State Univ, Fac Med, LV-1063 Riga, Latvia
[3] Int Univ Hlth & Welf, Otawara, Tochigi, Japan
基金
英国医学研究理事会;
关键词
melanocortin receptor subtypes; MSH; cAMP; ligand binding; HS014; SHU9119; rat;
D O I
10.1016/S0167-0115(02)00025-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The melanocortin 3 and 4 receptors are G-protein-coupled receptors found in the hypothalamus with important role in regulation of the energy balance. In this study, we performed pharmacological comparison of the rat and human melancortin (MC) 3 and MC4 receptors. We transiently expressed the genes for these receptors individually in a mammalian cell line and determined the binding affinities to several MSH peptides. The results showed no major difference between the rat and human MC3 receptors while the rat MC4 receptor had higher affinity to several peptides compared with the human MC4 receptor. NDP-, alpha-, beta-, gamma-MSH, ACTH(1-24), HS014 and MTII had from 5- to 34-fold higher affinity for the rat MC4 receptor, while SHU9119, HS024 and HS028 had similar affinity for both the MC4 receptors. pharmacological species difference have earlier been reported for the MC1 and MC5 receptors but this is the first report showing important differences between the rat and human MC4 receptors. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:7 / 12
页数:6
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