Malaisse-Lagae F, Mathias P C, Malaisse W J
Biochem Biophys Res Commun. 1984 Sep 28;123(3):1062-8. doi: 10.1016/s0006-291x(84)80241-7.
The organic calcium-antagonist nifedipine inhibits glucose-stimulated 45Ca net uptake and insulin release by rat pancreatic islets. However, the chemically related dihydropyridine derivative BAY K 8644 (methyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-(2-trifluoromethylphenyl)-pyridine-5- carboxylate) enhances 45Ca net uptake and insulin release and protects the B-cell against the inhibitory action of nifedipine. It is proposed that a regulatory site exists in or near the calcium channels, in the B-cell plasma membrane, and that occupation of this site by selected dihydropyridines may either facilitate or inhibit Ca2+ influx into the B-cell.
有机钙拮抗剂硝苯地平可抑制大鼠胰岛对葡萄糖刺激的45Ca净摄取及胰岛素释放。然而,化学结构相关的二氢吡啶衍生物BAY K 8644(1,4-二氢-2,6-二甲基-3-硝基-4-(2-三氟甲基苯基)-吡啶-5-羧酸甲酯)可增强45Ca净摄取及胰岛素释放,并保护B细胞免受硝苯地平的抑制作用。有人提出,在B细胞质膜的钙通道内或其附近存在一个调节位点,特定二氢吡啶占据该位点可能会促进或抑制Ca2+流入B细胞。