Leineweber K, Büscher R, Bruck H, Brodde O-E
Depts. of Pathophysiology and Nephrology, University of Essen School of Medicine, IG I., 9.OG, Hufelandstrasse 55, 45147, Essen, Germany.
Naunyn Schmiedebergs Arch Pharmacol. 2004 Jan;369(1):1-22. doi: 10.1007/s00210-003-0824-2. Epub 2003 Nov 28.
There can be no doubt that beta(1)-, beta(2)- and beta(3)-adrenoceptor genes have genetic polymorphisms. Two single nucleotide polymorphisms have been described for the beta(1)- (Ser49Gly; Gly389Arg), three for the beta(2)- (Arg16Gly; Gln27Glu; Thr164Ile) and one for the beta(3)-adrenoceptor subtype (Trp64Arg) that might be of functional importance. The possibility that changes in expression or properties of the beta-adrenoceptors due to single nucleotide polymorphisms might have phenotypic consequences influencing their cardiovascular or metabolic function or may contribute to the pathophysiology of several disorders like hypertension, congestive heart failure, asthma or obesity is an idea that has attracted much interest during the last 10 years. At present, it appears that these beta-adrenoceptor polymorphisms are very likely not disease-causing genes, but might be risk factors, might modify disease and/or might influence progression of disease. The aim of this review is to provide an overview of the functional consequences of such beta-adrenoceptor polymorphisms in vitro, ex vivo and in vivo.
毫无疑问,β(1)-、β(2)-和β(3)-肾上腺素能受体基因存在基因多态性。已描述了β(1)-肾上腺素能受体的两种单核苷酸多态性(Ser49Gly;Gly389Arg)、β(2)-肾上腺素能受体的三种单核苷酸多态性(Arg16Gly;Gln27Glu;Thr164Ile)以及β(3)-肾上腺素能受体亚型的一种单核苷酸多态性(Trp64Arg),这些多态性可能具有功能重要性。由于单核苷酸多态性导致β-肾上腺素能受体的表达或特性发生变化,进而可能产生影响其心血管或代谢功能的表型后果,或者可能促成高血压、充血性心力衰竭、哮喘或肥胖等多种疾病的病理生理学过程,这一观点在过去10年中引起了广泛关注。目前看来,这些β-肾上腺素能受体多态性很可能不是致病基因,但可能是危险因素,可能会改变疾病和/或影响疾病进展。本综述的目的是概述此类β-肾上腺素能受体多态性在体外、离体和体内的功能后果。