[Mechanism of action of beta-blockers].

X Martin
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Abstract

If beta-blockage does not cause lowering of aqueous humor secretion, in itself responsible for the maintenance of intraocular pressure, what is the mechanism of action? The antagonism for indolamines, recently measured in aqueous humor, the absence of nocturnal effect, and the amplitude diminution of diurnal variations thus produced suggest that beta-blockers could interact with indolamines, since the latter are probably responsible for intraocular pressure regulation. Aqueous humor secretion depends to a major extent on the sodium-potassium pump and its enzyme, Na+K(+)-ATPase. Serotonin, known for its activating action on Na+K(+)-ATPase, is present in the greatest amounts in the morning, precisely when the aqueous humor secretion is the highest. Moreover, timolol is a potent antagonist of serotonin, suggesting that beta-blockers could decrease the secretion by antagonism with serotonin at the level of Na+K(+)-ATPase. Since serotonin is metabolized to melatonin during sleep, beta-blockers might simulate a state of sleep of the ciliary epithelium.

[受体阻滞剂的作用机制]。
如果-阻滞剂不会降低房水分泌,而房水分泌本身负责维持眼压,那么作用机制是什么?最近在房水中测量到的对吲哚胺的拮抗作用,在夜间没有作用,并且由此产生的日变化幅度减小表明-受体阻滞剂可能与吲哚胺相互作用,因为后者可能负责眼压调节。房水分泌在很大程度上取决于钠钾泵及其酶Na+K(+)- atp酶。5 -羟色胺以其对Na+K(+)- atp酶的激活作用而闻名,它在早晨的含量最高,正是房水分泌最高的时候。此外,噻莫洛尔是一种有效的血清素拮抗剂,表明β受体阻滞剂可以通过在Na+K(+)- atp酶水平上拮抗血清素来减少血清素的分泌。由于5 -羟色胺在睡眠中被代谢为褪黑激素,β受体阻滞剂可能会模拟睫状上皮的睡眠状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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