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[肾上腺素能与甲状腺对能量代谢酶调节的相互关系及特点]

[Interrelations and characteristics of adrenergic and thyroid regulation of the enzymes of energy metabolism].

作者信息

Tapbergenov S O

出版信息

Probl Endokrinol (Mosk). 1982 Jul-Aug;28(4):67-73.

PMID:7122450
Abstract

In experiments on albino male rats it was detected that noradrenaline and adrenoxyl intensify the triiodothyronine-125I binding in myocardial and hepatic nucleus mitochondria. Under the action of adrenaline, triiodothyronine the binding is activated in myocardial mitochondria and is diminished in the cardias and hepatic nuclea. Thyroxin and adrenoxyl enhance noradrenaline-3H uptake by the auricular, myocardial and hepatic sections. Noradrenaline lowers noradrenaline-3H uptake by the auricular and myocardial sections. Hyperthyroidization is accompanied by a decrease in noradrenaline-3H uptake. beta-Adrenoreceptor block does not alter the thyroxine effect on the myocardial and hepatic succinatedehydrogenase, as well as on the hepatic ATPase. alpha-adrenoreceptor block does not influence the thyroxin effect upon the myocardial ATPase, but abolishes its activating action on the hepatic succinatedehydrogenase and ATPase. Realization of several thyroxin effects is associated to some extent with a functional adrenergic state. Catecholamine action on some mitochondrial enzymes is significantly stipulated by the effects of their monoamine oxidase and quinoid transformation products. The quinoid oxidation products of catecholamine render a regulatory effect both during the catecholamine and thyroid hormone accumulation stage and on the level of mitochondrial enzyme reception.

摘要

在对白化雄性大鼠的实验中发现,去甲肾上腺素和肾上腺色素可增强心肌和肝细胞核线粒体中三碘甲状腺原氨酸 - 125I 的结合。在肾上腺素作用下,三碘甲状腺原氨酸的结合在心肌线粒体中被激活,而在心脏和肝细胞核中则减少。甲状腺素和肾上腺色素可增强心房、心肌和肝组织对去甲肾上腺素 - 3H 的摄取。去甲肾上腺素可降低心房和心肌组织对去甲肾上腺素 - 3H 的摄取。甲状腺功能亢进伴随着去甲肾上腺素 - 3H 摄取的减少。β - 肾上腺素能受体阻断并不改变甲状腺素对心肌和肝琥珀酸脱氢酶以及肝 ATP 酶的作用。α - 肾上腺素能受体阻断并不影响甲状腺素对心肌 ATP 酶的作用,但可消除其对肝琥珀酸脱氢酶和 ATP 酶的激活作用。甲状腺素的几种作用在一定程度上与功能性肾上腺素能状态有关。儿茶酚胺对某些线粒体酶的作用在很大程度上受其单胺氧化酶和醌类转化产物的影响。儿茶酚胺的醌类氧化产物在儿茶酚胺和甲状腺激素积累阶段以及线粒体酶受体水平上均发挥调节作用。

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