Bridges R J, Nell G, Rummel W
J Physiol. 1983 May;338:463-75. doi: 10.1113/jphysiol.1983.sp014684.
Vasopressin enhanced the absorption of water and Na+ across everted sacs of rat colon descendens but had no effect on absorption across the colon ascendens. The short-circuit current (Isc) and open-circuit potential difference (p.d.) across the colon descendens were dose-dependently decreased by vasopressin. Isc and p.d. across the colon ascendens were not altered by vasopressin. In the colon descendens the decrease in Isc and p.d. was significant at 1 microu. vasopressin/ml and reached a maximum at 1 mu./ml. Propranolol and phentolamine or naloxone did not alter the decrease in Isc and p.d. to a submaximal dose of vasopressin. Vasopressin increased the mucosal to serosal flux of Na+ and Cl- and decreased the serosal to mucosal flux of Cl- across short-circuited colon descendens. Consequently these changes increased the net flux of Na+ and Cl-. Adenylate cyclase activity in homogenates of the colon descendens was not altered by vasopressin. Omission of Ca2+ from the serosal bathing solution reversibly decreased Isc and p.d. and increased Na+ and Cl- absorption across the colon descendens in a similar way as did vasopressin. The results suggest that the effect of vasopressin on the colon descendens may be due to a decrease in intracellular Ca2+ activity.
血管加压素可增强大鼠降结肠外翻囊对水和钠离子的吸收,但对升结肠的吸收无影响。血管加压素可使降结肠的短路电流(Isc)和开路电位差(p.d.)呈剂量依赖性降低。血管加压素对升结肠的Isc和p.d.无影响。在降结肠中,当血管加压素浓度为1微单位/毫升时,Isc和p.d.的降低具有显著性,在1单位/毫升时达到最大值。普萘洛尔、酚妥拉明或纳洛酮均不能改变血管加压素亚最大剂量引起的Isc和p.d.的降低。血管加压素增加了短路降结肠黏膜到浆膜的钠离子和氯离子通量,并降低了浆膜到黏膜的氯离子通量。因此,这些变化增加了钠离子和氯离子的净通量。血管加压素对降结肠匀浆中的腺苷酸环化酶活性无影响。从浆膜浴液中去除钙离子可使Isc和p.d.可逆性降低,并增加降结肠对钠离子和氯离子的吸收,其作用方式与血管加压素相似。结果表明,血管加压素对降结肠的作用可能是由于细胞内钙离子活性降低所致。