Sjöqvist A, Henderson L S, Fondacaro J D
Proc Soc Exp Biol Med. 1986 Jul;182(3):404-8. doi: 10.3181/00379727-182-42359.
Studies were designed to examine the effects of phorbol esters on intestinal fluid transport and blood flow in the anesthetized cat and enteropooling in the conscious rat. Intraluminal administration of phorbol ester into a segment of isolated small bowel produced a copious intestinal secretion and a concomitant mesenteric hyperemia in the cat. Net fluid movement in the intestine was converted from absorption in the control state to secretion following phorbol ester administration. Intravenous atropine reduced the phorbol ester-induced secretion by 56%; clonidine abolished the remaining secretory response. In the rat, intragastric administration of phorbol ester produced enteropooling comparable to that of other potent intestinal secretagogues. Since phorbol esters are known to activate protein kinase C, these studies suggest that activation of protein kinase C in the small intestine may lead to a full secretory response. The evidence suggests that this secretion is accompanied by a metabolic hyperemia. These results suggest that protein kinase C plays an important role in the regulation of intestinal fluid transport.
研究旨在检测佛波酯对麻醉猫肠液转运和血流以及清醒大鼠肠内液体积聚的影响。向猫的一段离体小肠腔内给予佛波酯可产生大量肠分泌以及伴随的肠系膜充血。给予佛波酯后,肠内的净液体移动从对照状态下的吸收转变为分泌。静脉注射阿托品可使佛波酯诱导的分泌减少56%;可乐定消除了剩余的分泌反应。在大鼠中,胃内给予佛波酯产生的肠内液体积聚与其他强效肠促分泌剂相当。由于已知佛波酯可激活蛋白激酶C,这些研究提示小肠中蛋白激酶C的激活可能导致完全的分泌反应。有证据表明这种分泌伴随着代谢性充血。这些结果提示蛋白激酶C在肠液转运的调节中起重要作用。