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Endogenous cardiotonic steroids.

机译:内源性强心类固醇。

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The search for endogenous digitalis led to the isolation of ouabain from blood adrenals and hypothalamus. Additional cardiotonic steroids of the cardenolid and bufadienolide type seem to circulate in blood. Adrenal cortical cells in tissue culture release ouabain upon addition of angiotensin 11. Ouabain in blood is increased in 50% of Caucasians with low renin hypertension. Analogous to other steroid hormones, cardiotonic steroid hormones in blood are bound to a specific cardiac glycoside binding globulin. Since ouabain induced growth of myocytes in tissue culture, this effect probably mediates by partial inhibition of the sodium pump and consecutive rise of intracellular Ca2+ the thickening of the wall of arteries and myocardium. PST 2238, an antagonist of cardiac glycoside function at the sodium pump, leads in rats under prolonged therapy to a decrease of hypertension. The finding of ouabain as a new adrenal hormone of the Na+ metabolism and of ouabain antagonists opens new possibilities of therapy of hypertension and congestive heart failure.
机译:对内源性洋地黄的搜寻导致哇巴因与血液肾上腺和下丘脑分离。卡尼多利德和布法非烯利德类型的其他强心类固醇似乎在血液中循环。添加血管紧张素11后,组织培养物中的肾上腺皮质细胞释放哇巴因。低肾素高血压的高加索人中50%的血液中哇巴因增加。与其他类固醇激素类似,血液中的强心类固醇激素与特定的心脏糖苷结合球蛋白结合。由于哇巴因在组织培养中诱导了心肌细胞的生长,这种作用可能通过钠泵的部分抑制和细胞内Ca2 +的连续升高,动脉和心肌壁的增厚来介导。 PST 2238是钠泵上心脏糖苷功能的拮抗剂,可导致长时间治疗的大鼠高血压降低。哇巴因作为一种新的Na +代谢肾上腺激素和哇巴因拮抗剂的发现为高血压和充血性心力衰竭的治疗开辟了新的可能性。

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