Altan V Melih, Arioglu Ebru, Guner Sahika, Ozcelikay A Tanju
Department of Pharmacology, Faculty of Pharmacy, University of Ankara, Tandogan, Ankara, 06100, Turkey.
Heart Fail Rev. 2007 Mar;12(1):58-65. doi: 10.1007/s10741-007-9005-6. Epub 2007 Mar 16.
Despite the significant developments in the treatment of diabetes mellitus, diabetic patients still continue to suffer from cardiac complications. The increase of cardiac adrenergic drive may ultimately contribute to the development and progression of diabetic cardiomyopathy. beta-Adrenoceptors play an important role in the regulation of heart function. However, responsiveness of diabetic heart to beta-adrenoceptor agonist stimulation is diminished. The chronotropic responses mediated by beta(1)-subtype, which is mainly responsible for cardiac effects of catecholamines are decreased in the atria of diabetic rats. The expression of cardiac beta(1)-subtype is significantly decreased in diabetic rats as well. beta(2)-Adrenoceptors also increase cardiac function. Although the expression of this subtype is slightly decreased in diabetic rat hearts, beta(2)-mediated chronotropic responses are preserved. On the other hand, functional beta(3)-adrenoceptor subtype was characterized in human heart. Interestingly, stimulation of cardiac beta(3)-adrenoceptors, on the contrary of beta(1)- and beta(2)-subtypes, mediates negative inotropic effect in human ventricular muscle. Cardiac beta(3)-adrenoceptors are upregulated in experimental diabetes as well as in human heart failure. These findings suggest that each beta-adrenoceptor subtype may play an important role in the pathophysiology of diabetes-induced heart disease. However, it is still not known whether the changes in the expression and/or responsiveness of beta-adrenoceptors are adaptive or maladaptive. Therefore, this review outlines the potential roles of these receptor subtypes in cardiac pathologies of diabetes.
尽管糖尿病治疗取得了重大进展,但糖尿病患者仍继续遭受心脏并发症的困扰。心脏肾上腺素能驱动的增加最终可能导致糖尿病性心肌病的发生和发展。β-肾上腺素能受体在心脏功能调节中起重要作用。然而,糖尿病心脏对β-肾上腺素能受体激动剂刺激的反应性降低。由β₁亚型介导的变时反应主要负责儿茶酚胺的心脏效应,在糖尿病大鼠心房中降低。糖尿病大鼠心脏中β₁亚型的表达也显著降低。β₂-肾上腺素能受体也可增强心脏功能。虽然该亚型在糖尿病大鼠心脏中的表达略有降低,但β₂介导的变时反应得以保留。另一方面,功能性β₃-肾上腺素能受体亚型在人类心脏中得到了表征。有趣的是,与β₁和β₂亚型相反,刺激心脏β₃-肾上腺素能受体在人类心室肌中介导负性肌力作用。在实验性糖尿病以及人类心力衰竭中,心脏β₃-肾上腺素能受体均上调。这些发现表明,每种β-肾上腺素能受体亚型可能在糖尿病性心脏病的病理生理学中起重要作用。然而,β-肾上腺素能受体的表达和/或反应性变化是适应性还是适应不良仍不清楚。因此,本综述概述了这些受体亚型在糖尿病心脏病变中的潜在作用。