Ho A K, Ceña V, Klein D C
Biochem Biophys Res Commun. 1987 Feb 13;142(3):819-25. doi: 10.1016/0006-291x(87)91487-2.
Ouabain and related cardiac glycosides stimulate phospholipase C activity 5-fold in rat pinealocytes. The combined treatment of ouabain and norepinephrine, which also stimulates phospholipase C, produces an additive effect. The effects of either ouabain or norepinephrine are blocked by EGTA. However, there are notable differences. The stimulatory effect of ouabain is lost when extracellular Na+ is reduced to 20 mM and is not blocked by prazosin. In contrast, the stimulatory effect of norepinephrine is not blocked when extracellular Na+ is reduced to 20 mM but is blocked by prazosin. Ouabain appears to increase phospholipase C activity through a mechanism involving inhibition of Na+,K+-ATPase, and an accumulation of intracellular Na+ and Ca2+, not involving alpha 1-adrenoceptors. These findings raise the possibility that activation of phospholipase C might be a more general effect of cardiac glycosides.
哇巴因及相关强心苷可使大鼠松果体细胞中的磷脂酶C活性提高5倍。哇巴因与去甲肾上腺素联合处理(去甲肾上腺素也可刺激磷脂酶C)可产生相加效应。哇巴因或去甲肾上腺素的作用均被乙二醇双四乙酸(EGTA)阻断。然而,二者存在显著差异。当细胞外钠离子浓度降至20 mM时,哇巴因的刺激作用消失,且不受哌唑嗪阻断。相反,当细胞外钠离子浓度降至20 mM时,去甲肾上腺素的刺激作用不受阻断,但受哌唑嗪阻断。哇巴因似乎通过一种涉及抑制钠钾ATP酶、细胞内钠离子和钙离子蓄积的机制来增加磷脂酶C活性,而不涉及α1 -肾上腺素能受体。这些发现增加了磷脂酶C的激活可能是强心苷更普遍作用的可能性。