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大鼠心肌肾上腺素能受体的甲状腺依赖性改变及肾上腺素能受体介导的反应

Thyroid-dependent alterations of myocardial adrenoceptors and adrenoceptor-mediated responses in the rat.

作者信息

Gross G, Lues I

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1985 Jun;329(4):427-39. doi: 10.1007/BF00496378.

Abstract

Cardiovascular alterations in hypo- and hyperthyroidism have been ascribed to changes of noradrenergic neurotransmission. In the present study the influence of thyroid hormones on adrenoceptors in the rat heart was further characterized. The effect of artificial hypothyroidism (induced by feeding 6-propyl-2-thiouracil, PTU) and hyperthyroidism (induced by daily injections of triiodothyronine, T3) on myocardial adrenoceptor binding, catecholamines, some physiological responses, and their interdependence was examined. The density of myocardial beta-adrenergic binding sites (3H-dihydroalprenolol, 3H-DHA) was reduced after PTU (by 38%) and enhanced after T3 treatment (by up to 82%). The increase was dose- and time-dependent and reversible within 4 days. No changes of the affinity of 3H-DHA to its binding sites were observed. Only L-T3 and L-T4 proved to be active, D-T3 and reverse T3 had no effect. The rise in beta-adrenoceptor density caused by T3 was prevented by concomitant administration of cycloheximide, indicating its dependence on protein synthesis. The density of myocardial alpha 1-adrenergic binding sites (3H-prazosin) was significantly reduced in the PTU group (by up to 28%) and even more distinctly by T3 treatment (by up to 50%). KD values remained unaltered. The noradrenaline content and turnover of rat hearts was significantly reduced by T3-induced hyperthyroidism. PTU treatment had no influence on content and turnover of noradrenaline. Plasma noradrenaline as well as adrenaline levels in freely moving rats were increased by PTU treatment 9- and 5-fold, respectively. In T3-injected animals no significant changes were measured. The density of adrenoceptors is known to be inversely correlated with catecholamine levels in several organs. Neither alpha- nor beta-adrenoceptor changes in the myocardium of dysthyroid rats could be attributed to such a homologous regulation, since they still occurred after chemical sympathectomy with 6-hydroxydopamine and adrenalectomy.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

甲状腺功能减退和亢进时的心血管改变被认为与去甲肾上腺素能神经传递的变化有关。在本研究中,进一步探讨了甲状腺激素对大鼠心脏肾上腺素能受体的影响。研究了人工诱导的甲状腺功能减退(通过喂食6-丙基-2-硫氧嘧啶,PTU)和甲状腺功能亢进(通过每日注射三碘甲状腺原氨酸,T3)对心肌肾上腺素能受体结合、儿茶酚胺、一些生理反应及其相互关系的影响。PTU处理后心肌β-肾上腺素能结合位点(3H-二氢阿普洛尔,3H-DHA)密度降低(降低38%),T3处理后升高(最高可达82%)。这种增加呈剂量和时间依赖性,且在4天内可逆。未观察到3H-DHA与其结合位点亲和力的变化。只有L-T3和L-T4具有活性,D-T3和反式T3无作用。T3引起的β-肾上腺素能受体密度升高可被同时给予的环己酰亚胺阻止,表明其依赖于蛋白质合成。PTU组心肌α1-肾上腺素能结合位点(3H-哌唑嗪)密度显著降低(最高可达28%),T3处理使其降低更明显(最高可达50%)。解离常数(KD)值保持不变。T3诱导的甲状腺功能亢进使大鼠心脏去甲肾上腺素含量和周转率显著降低。PTU处理对去甲肾上腺素含量和周转率无影响。自由活动大鼠经PTU处理后,血浆去甲肾上腺素和肾上腺素水平分别升高9倍和5倍。注射T3的动物未检测到显著变化。已知在几个器官中,肾上腺素能受体密度与儿茶酚胺水平呈负相关。甲状腺功能异常大鼠心肌中的α-和β-肾上腺素能受体变化均不能归因于这种同源调节,因为在使用6-羟基多巴胺进行化学交感神经切除术和肾上腺切除术后,这些变化仍然存在。(摘要截选至400字)

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