Roesler Rafael, Kapczinski Flávio, Quevedo João, Dal Pizzol Felipe, Schwartsmann Gilberto
Cellular and Molecular Neuropharmacology Research Group, Department of Pharmacology, Institute for Basic Health Sciences, Federal University of Rio Grande do Sul, 90046-900 Porto Alegre, RS, Brazil.
Recent Pat CNS Drug Discov. 2007 Jun;2(2):125-9. doi: 10.2174/157488907780832742.
Gastrin-releasing peptide (GRP) is a mammalian counterpart of the amphibian peptide bombesin (BB) that stimulates cell proliferation, acts as a growth factor in the pathogenesis of many types of cancer, and regulates several aspects of neuroendocrine function. BB and GRP act by binding to the GRP-preferring type of BB receptor (GRPR, also known as BB2 receptor), a member of the superfamily of G-protein coupled membrane receptors. This review summarizes recent evidence from animal and human studies indicating that abnormalities in GRPR function in the brain might play a role in the pathogenesis of neurological and psychiatric disorders, and suggesting that BB, GRP, and GRPR antagonists might display therapeutic actions in central nervous system diseases. Recent patent applications on GRPR-related methods for treating brain disorders are introduced.
胃泌素释放肽(GRP)是两栖类动物促胃液素释放肽(BB)在哺乳动物中的对应物,它能刺激细胞增殖,在多种癌症的发病机制中作为一种生长因子,并调节神经内分泌功能的多个方面。BB和GRP通过与偏好GRP的BB受体类型(GRPR,也称为BB2受体)结合发挥作用,GRPR是G蛋白偶联膜受体超家族的成员。本综述总结了来自动物和人体研究的最新证据,这些证据表明大脑中GRPR功能异常可能在神经和精神疾病的发病机制中起作用,并提示BB、GRP和GRPR拮抗剂可能在中枢神经系统疾病中显示出治疗作用。还介绍了近期关于GRPR相关治疗脑部疾病方法的专利申请。