Ziegelhöffer A, Dzurba A, Vrbjar N, Styk J, Slezák J
Ustavu experimentálnej chirurgie CFV SAV v Bratislave.
Bratisl Lek Listy. 1990 Dec;91(12):902-10.
Today it is accepted that estrogens mitigate the consequences of ischemic heart disease. Preliminary experiments revealed an increase in heart sarcolemmal (Na+ + K+)-ATPase activity after application of estradiol in vivo. It is also well known the key role of latter enzyme for heart function. The facts mentioned above indicate that estradiol may act on the heart just via modulation of the (Na+ + K+)-ATPase activity. In present paper it is confirmed that 17-beta-estradiol stimulates the activity of sarcolemmal (Na+ + K+)-ATPase by allosteric manner, particularly by increasing positive cooperativity between the K(+)-binding sites of the enzyme. This effect is manifested by enhancement in functional capacity of the sodium pump in sarcolemma. Stimulatory effect of estradiol is bound to integrated myocytes: neither is it manifested in isolated sarcolemma in vitro nor exhibits any influence on the affinity of binding sites for cardiac glycosides or on total capacity of the sarcolemma to bind ouabain. Basing on the data obtained it was assumed that estradiol acts on the (Na+ + K+)-ATPase not directly but by means of a mediator released within the myocyte.
如今,雌激素可减轻缺血性心脏病后果这一观点已被广泛接受。初步实验表明,在体内应用雌二醇后,心脏肌膜(Na⁺ + K⁺)-ATP酶活性会增加。而后一种酶对心脏功能的关键作用也广为人知。上述事实表明,雌二醇可能正是通过调节(Na⁺ + K⁺)-ATP酶活性来作用于心脏。在本论文中得到证实的是,17-β-雌二醇通过变构方式刺激肌膜(Na⁺ + K⁺)-ATP酶的活性,特别是通过增加该酶K⁺结合位点之间的正协同性。这种效应表现为肌膜中钠泵功能能力的增强。雌二醇的刺激作用与完整的心肌细胞相关:它在体外分离的肌膜中既不表现出来,对心肌苷结合位点的亲和力或肌膜结合哇巴因的总能力也没有任何影响。基于所获得的数据推测,雌二醇并非直接作用于(Na⁺ + K⁺)-ATP酶,而是借助心肌细胞内释放的一种介质发挥作用。