Schoner W
Institut für Biochemie und Endokrinologie, Fachbereich Veterinärmedizin, Justus-Liebig-Universität Giessen, Germany.
Cell Mol Biol (Noisy-le-grand). 2001 Mar;47(2):273-80.
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.
对内源性洋地黄的研究导致从血液、肾上腺和下丘脑分离出哇巴因。其他强心甾类(强心甾烯蟾毒类和蟾毒配基类)似乎在血液中循环。组织培养中的肾上腺皮质细胞在添加血管紧张素II后会释放哇巴因。50%的低肾素性高血压白种人血液中的哇巴因含量会升高。与其他甾体激素类似,血液中的强心甾类激素与一种特定的强心苷结合球蛋白结合。由于哇巴因在组织培养中可诱导心肌细胞生长,这种作用可能是通过部分抑制钠泵以及随后细胞内Ca2+升高,进而导致动脉壁和心肌壁增厚来介导的。PST 2238是一种作用于钠泵的强心苷功能拮抗剂,在大鼠长期治疗中可导致高血压降低。哇巴因作为一种新的钠代谢肾上腺激素以及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。