Imbrogno S, Gattuso A, Mazza R, Angelone T, Cerra M C
Department of Biology, Ecology and Earth Sciences, University of Calabria, Arcavacata di Rende, Italy.
National Institute of Cardiovascular Research, Bologna, Italy.
Acta Physiol (Oxf). 2015 Jun;214(2):158-75. doi: 10.1111/apha.12493. Epub 2015 Apr 6.
Recent cardiovascular research showed that, together with β1- and β2-adrenergic receptors (ARs), β3-ARs contribute to the catecholamine (CA)-dependent control of the heart. β3-ARs structure, function and ligands were investigated in mammals because of their applicative potential in human cardiovascular diseases. Only recently, the concept of a β3-AR-dependent cardiac modulation was extended to non-mammalian vertebrates, although information is still scarce and fragmentary. β3-ARs were structurally described in fish, showing a closer relationship to mammalian β1-AR than β2-AR. Functional β3-ARs are present in the cardiac tissue of teleosts and amphibians. As in mammals, activation of these receptors elicits a negative modulation of the inotropic performance through the involvement of the endothelium endocardium (EE), Gi/0 proteins and the nitric oxide (NO) signalling. This review aims to comparatively analyse data from literature on β3-ARs in mammals, with those on teleosts and amphibians. The purpose is to highlight aspects of uniformity and diversity of β3-ARs structure, ligands activity, function and signalling cascades throughout vertebrates. This may provide new perspectives aimed to clarify the biological relevance of β3-ARs in the context of the nervous and humoral control of the heart and its functional plasticity.
近期的心血管研究表明,β3-肾上腺素能受体(ARs)与β1-和β2-肾上腺素能受体一起,参与了儿茶酚胺(CA)对心脏的依赖性调控。由于β3-ARs在人类心血管疾病中的应用潜力,人们对其在哺乳动物中的结构、功能和配体进行了研究。直到最近,β3-AR依赖性心脏调节的概念才扩展到非哺乳动物脊椎动物,不过相关信息仍然匮乏且零散。鱼类中已对β3-ARs进行了结构描述,结果显示其与哺乳动物β1-AR的关系比与β2-AR的关系更为密切。硬骨鱼和两栖动物的心脏组织中存在功能性β3-ARs。与哺乳动物一样,这些受体的激活通过内皮心内膜(EE)、Gi/0蛋白和一氧化氮(NO)信号传导,对心肌收缩性能产生负调节作用。本综述旨在对哺乳动物、硬骨鱼和两栖动物β3-ARs的文献数据进行比较分析。目的是突出整个脊椎动物β3-ARs在结构、配体活性、功能和信号级联方面的一致性和多样性。这可能会提供新的视角,以阐明β3-ARs在心脏神经和体液控制及其功能可塑性背景下的生物学相关性。