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先天性心脏病患儿心肌β-肾上腺素能受体亚型的分布及其与腺苷酸环化酶的偶联关系及治疗意义

Distribution of myocardial beta-adrenoceptor subtypes and coupling to the adenylate cyclase in children with congenital heart disease and implications for treatment.

作者信息

Kozlik-Feldmann R, Kramer H H, Wicht H, Feldmann R, Netz H, Reinhardt D

机构信息

Children's Hospital, Ludwig-Maximilians-University of Munich, Germany.

出版信息

J Clin Pharmacol. 1993 Jul;33(7):588-95. doi: 10.1002/j.1552-4604.1993.tb04709.x.

Abstract

In congestive heart failure, down-regulation of myocardial beta-adrenoceptors (beta-AR) due to an elevated sympathetic tone is well known. In infancy and childhood, heart failure is usually related to congenital heart disease (CHD). Therefore, 71 samples of right atrial tissue of infants and children with CHD undergoing cardiac surgery were studied for beta-adrenoceptor density and distribution of the beta 1-/beta 2-AR subtypes. In 49 cases, the coupling of the beta-AR to the adenylate cyclase (AC) was examined. In a further study of 19 myocardial samples, AC was selectively stimulated with beta 1- or beta 2-AR whereas the other subtype was blocked by an antagonist. The following results were obtained: (1) Infants and children with severe acyanotic or cyanotic CHD had severely reduced beta-AR densities. (2) In most of the cases, the beta-AR down regulation is beta 1-subtype selective, but in critically ill newborns with congenital aortic valve stenosis or transposition of the great arteries, there is additional significant beta 2-AR down-regulation. In Fallot patients treated with the beta-antagonist propranolol, a significant increased beta-AR number compared with untreated Fallot patients was found. (3) beta-Adrenoceptor reduction in CHD is correlated with elevated noradrenaline plasma levels, thus proving a sympathetic dysregulation. (4) In CHD with moderate hemodynamic load, beta 2-AR coupling to AC was markedly more efficient than beta 1-AR coupling. The small number of myocardial beta 2-AR produced most of the cyclic adenosine monophosphate. (5) In severe acyanotic and cyanotic CHD, a partial decoupling of the beta 2-AR to the AC occurred.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在充血性心力衰竭中,由于交感神经张力升高导致心肌β - 肾上腺素能受体(β - AR)下调是众所周知的。在婴儿期和儿童期,心力衰竭通常与先天性心脏病(CHD)有关。因此,对71例接受心脏手术的CHD婴幼儿的右心房组织样本进行了β - 肾上腺素能受体密度及β1 - /β2 - AR亚型分布的研究。在49例病例中,检测了β - AR与腺苷酸环化酶(AC)的偶联情况。在另外一项对19个心肌样本的研究中,用β1 - 或β2 - AR选择性刺激AC,而另一种亚型则被拮抗剂阻断。得到了以下结果:(1)患有严重非紫绀型或紫绀型CHD的婴幼儿β - AR密度严重降低。(2)在大多数情况下,β - AR下调是β1亚型选择性的,但在患有先天性主动脉瓣狭窄或大动脉转位的危重新生儿中,还存在显著的β2 - AR下调。在接受β - 拮抗剂普萘洛尔治疗的法洛四联症患者中,发现其β - AR数量比未治疗的法洛四联症患者显著增加。(3)CHD中β - 肾上腺素能受体减少与血浆去甲肾上腺素水平升高相关,从而证明存在交感神经调节异常。(4)在血流动力学负荷中等的CHD中,β2 - AR与AC的偶联明显比β1 - AR偶联更有效。少量的心肌β2 - AR产生了大部分的环磷酸腺苷。(5)在严重非紫绀型和紫绀型CHD中,β2 - AR与AC发生了部分解偶联。(摘要截选至250词)

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