Pento J T, Johnson M E
Pharmacology. 1983;27(6):343-9. doi: 10.1159/000137890.
The effects of verapamil on calcium transport and uptake in duodenal and jejunal segments of intestine in young male rats were determined using the everted gut-sac technique. Verapamil added to both the mucosal and serosal surface of duodenal segments decreased calcium transport and tissue uptake in a dose-related fashion over a concentration range of 1-2 mM. In jejunal segments verapamil (1 mM) added to both the mucosal and serosal surface reduced calcium transport but did not alter tissue uptake. Similarly, verapamil (1 mM) added to either the mucosal or serosal surface alone in duodenal segments reduced transport but did not depress tissue uptake. The results of this study indicate that verapamil alters calcium translocation in intestinal tissue in a fashion which is similar to that reported in other biological tissue.
采用外翻肠囊技术测定了维拉帕米对年轻雄性大鼠十二指肠和空肠段钙转运及摄取的影响。在十二指肠段的黏膜和浆膜表面添加维拉帕米,在1 - 2 mM的浓度范围内,钙转运和组织摄取呈剂量相关方式降低。在空肠段,在黏膜和浆膜表面添加维拉帕米(1 mM)可降低钙转运,但不改变组织摄取。同样,仅在十二指肠段的黏膜或浆膜表面添加维拉帕米(1 mM)可降低转运,但不抑制组织摄取。本研究结果表明,维拉帕米以类似于其他生物组织中报道的方式改变肠道组织中的钙转运。