Morita K, Hamano S, Yoshizumi M, Oka M
Department of Pharmacology, Tokushima University School of Medicine, Japan.
Biochem Pharmacol. 1989 Dec 15;38(24):4461-5. doi: 10.1016/0006-2952(89)90657-6.
The effect of carvediolol on the secretory function was studied using cultured bovine adrenal chromaffin cells. Carvedilol caused the concentration-dependent inhibition of catecholamine secretion evoked by carbamylcholine, high K+ or veratridine. The drug also caused the inhibition of radioactive calcium uptake stimulated by these secretagogues into the cells, and the inhibition of calcium uptake was observed in parallel with that of catecholamine secretion. The inhibitory action of carvedilol on catecholamine secretion was shown to be similar to that caused by a classical beta-adrenoceptor antagonist, propranolol. Furthermore, although the level of carbamylcholine-stimulated catecholamine secretion inhibited by diltiazem, a potent calcium channel antagonist, was significantly raised by elevating the calcium concentration in the reaction mixture, increasing the concentration of calcium ions in the mixture failed to induce any substantial influence on the secretion inhibited by carvedilol, as well as propranolol, under the same experimental conditions. These results seem to indicate that carvedilol may cause the inhibition of catecholamine secretion through its blocking action on calcium influx into the cells, and suggest the possibility that the inhibitory action of carvedilol on calcium influx is presumably based on its stabilizing action on the plasma membranes rather than its blocking action on the calcium channels in the chromaffin cell.
使用培养的牛肾上腺嗜铬细胞研究了卡维地洛对分泌功能的影响。卡维地洛可浓度依赖性地抑制由氨甲酰胆碱、高钾或藜芦碱诱发的儿茶酚胺分泌。该药物还可抑制这些促分泌剂刺激细胞摄取放射性钙,并且观察到钙摄取的抑制与儿茶酚胺分泌的抑制平行。卡维地洛对儿茶酚胺分泌的抑制作用与经典β-肾上腺素能受体拮抗剂普萘洛尔所引起的作用相似。此外,虽然强效钙通道拮抗剂地尔硫卓抑制的氨甲酰胆碱刺激的儿茶酚胺分泌水平可通过提高反应混合物中的钙浓度而显著升高,但在相同实验条件下,增加混合物中钙离子浓度对卡维地洛以及普萘洛尔所抑制的分泌未产生任何实质性影响。这些结果似乎表明,卡维地洛可能通过其对细胞内钙内流的阻断作用来抑制儿茶酚胺分泌,并提示卡维地洛对钙内流的抑制作用可能基于其对质膜的稳定作用而非对嗜铬细胞中钙通道的阻断作用。