Beau S L, Tolley T K, Saffitz J E
Department of Pathology, Washington University School of Medicine, St Louis, Mo 63110.
Circulation. 1993 Dec;88(6):2501-9. doi: 10.1161/01.cir.88.6.2501.
Downregulation of myocardial beta-adrenergic receptor density does not occur in a spatially uniform distribution in patients with congestive heart failure. Rather, it results primarily from loss of receptors in the subendocardium. In patients with dilated cardiomyopathy, beta 1-receptors have been found to be downregulated selectively. These observations suggest that considerable transmural heterogeneity in the distribution of beta-adrenergic receptor subtypes exists in the failing human heart. The present study was designed to test this hypothesis.
We used quantitative autoradiography of radioligand binding sites to measure the distribution of beta-adrenergic receptor subtypes in transmural sections of left ventricular myocardium obtained from cardiac transplant patients with ischemic (n = 13) and idiopathic dilated (n = 12) cardiomyopathy and from 4 subjects with no history of cognitive heart failure. Analysis of radioligand binding isotherms revealed a significant reduction in total beta-adrenergic receptor density in hearts of patients with ischemic and idiopathic cardiomyopathy (20.3 +/- 1.9 and 18.2 +/- 2.0 fmol/mg protein, respectively, versus 40.0 +/- 11.4 in control subjects; P < .01 for both). Loss of the beta 1-subtype accounted for 86% of the total reduction in beta-receptor density in failing hearts. Despite the significant decreases in overall tissue receptor content, the densities of total beta-receptors and beta-receptor subtypes in subepicardial myocytes were equivalent in failing and control hearts. However, in contrast to control hearts, in which the transmural distribution of total and beta 1-receptors was uniform (endocardial: epicardial receptor density ratios, 0.97 +/- 0.14 and 1.0 +/- 0.2, respectively), hearts of patients with ischemic and idiopathic dilated cardiomyopathy had significantly lower total beta-receptor and beta 1-receptor densities in the subendocardium (ratios, 0.66 +/- 0.06 and 0.46 +/- 0.09 for total and beta 1-receptors, respectively, in ischemic cardiomyopathy and 0.60 +/- 0.08 and 0.52 +/- 0.11 in dilated cardiomyopathy; P < .001 for all values compared with a ratio of 1). Thus, beta 1: beta 2 receptor density ratios were markedly decreased in the subendocardium of ischemic and idiopathic dilated left ventricles compared with control hearts.
A significant transmural gradient in the density of myocardial beta 1-adrenergic receptors exists in the hearts of patients with ischemic and dilated cardiomyopathy, resulting in a markedly altered beta 1: beta 2 receptor density ratio in the subendocardium.
在充血性心力衰竭患者中,心肌β-肾上腺素能受体密度的下调并非呈空间均匀分布。相反,它主要是由于心内膜下受体的丧失所致。在扩张型心肌病患者中,已发现β1受体被选择性下调。这些观察结果表明,在衰竭的人类心脏中,β-肾上腺素能受体亚型的分布存在显著的透壁异质性。本研究旨在验证这一假设。
我们使用放射性配体结合位点的定量放射自显影术,测量了从患有缺血性心肌病(n = 13)和特发性扩张型心肌病(n = 12)的心脏移植患者以及4名无充血性心力衰竭病史的受试者获取的左心室心肌透壁切片中β-肾上腺素能受体亚型的分布。放射性配体结合等温线分析显示,缺血性和特发性心肌病患者心脏中的总β-肾上腺素能受体密度显著降低(分别为20.3±1.9和18.2±2.0 fmol/mg蛋白质,而对照组为40.0±11.4;两者P均<0.01)。β1亚型的丧失占衰竭心脏中β受体密度总降低量的86%。尽管整体组织受体含量显著降低,但衰竭心脏和对照心脏的心外膜下心肌细胞中总β受体和β受体亚型的密度相当。然而,与对照心脏不同,对照心脏中总受体和β1受体的透壁分布是均匀的(心内膜:心外膜受体密度比分别为0.97±0.14和1.0±0.2),缺血性和特发性扩张型心肌病患者心脏的心内膜下总β受体和β1受体密度显著降低(缺血性心肌病中总受体和β1受体的比值分别为0.66±0.06和0.46±0.09,扩张型心肌病中为0.60±0.08和0.52±0.11;与比值1相比,所有值P均<0.001)。因此,与对照心脏相比,缺血性和特发性扩张型左心室心内膜下的β1:β2受体密度比显著降低。
在缺血性和扩张型心肌病患者的心脏中,心肌β1-肾上腺素能受体密度存在显著的透壁梯度,导致心内膜下β1:β2受体密度比明显改变。