Wada A, Izumi F, Yanagihara N, Kobayashi H
Naunyn Schmiedebergs Arch Pharmacol. 1985 Jan;328(3):273-8. doi: 10.1007/BF00515553.
The effects of ouabain and diphenylhydantoin on the secretion of catecholamines induced by veratridine were investigated in cultured bovine adrenal medullary cells with special reference to ion fluxes. Veratridine itself induced an influx of 22Na and 45Ca as well as secretion of catecholamines, which were antagonized by tetrodotoxin, a selective inhibitor of voltage dependent Na channels. The secretion of catecholamines caused by veratridine was not observed either in Na free or Ca free medium. Veratridine-induced influx of 45Ca did not occur in Na free medium, while veratridine-induced influx of 22Na occurred even in Ca free medium. Veratridine-induced influx of 22Na, 45Ca and secretion of catecholamines were all potentiated by ouabain, a potent inhibitor of Na,K-ATPase. Omission of K from the medium, a condition which suppresses the Na,K-ATPase activity, also augmented these cell responses caused by veratridine. On the contrary, diphenylhydantoin, which is known to decrease the intracellular concentration of Na, reduced the veratridine-induced influx of 22Na, 45Ca and secretion of catecholamines. The potentiating effects of ouabain on the veratridine-induced cell responses were all abolished by diphenylhydantoin. These findings imply that veratridine, ouabain and K removal as well as diphenylhydantoin modulate the intracellular accumulation of 22Na which is involved in the influx of 45Ca and the secretion of catecholamines.
研究了哇巴因和苯妥英钠对藜芦碱诱导的儿茶酚胺分泌的影响,实验采用培养的牛肾上腺髓质细胞,并特别关注离子通量。藜芦碱本身可诱导22Na和45Ca内流以及儿茶酚胺分泌,这些效应可被电压依赖性Na通道的选择性抑制剂河豚毒素所拮抗。在无Na或无Ca培养基中未观察到藜芦碱引起的儿茶酚胺分泌。藜芦碱诱导的45Ca内流在无Na培养基中不发生,而藜芦碱诱导的22Na内流即使在无Ca培养基中也会发生。藜芦碱诱导的22Na、45Ca内流以及儿茶酚胺分泌均被Na,K-ATP酶的强效抑制剂哇巴因增强。培养基中去除K(一种抑制Na,K-ATP酶活性的条件)也增强了藜芦碱引起的这些细胞反应。相反,已知可降低细胞内Na浓度的苯妥英钠减少了藜芦碱诱导的22Na、45Ca内流以及儿茶酚胺分泌。哇巴因对藜芦碱诱导的细胞反应的增强作用均被苯妥英钠消除。这些发现表明,藜芦碱、哇巴因、K的去除以及苯妥英钠可调节22Na在细胞内的蓄积,而22Na的蓄积与45Ca内流和儿茶酚胺分泌有关。