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血管紧张素II和去甲肾上腺素可拮抗血管活性肠肽对大鼠回肠和结肠的分泌作用。

Angiotensin II and norepinephrine antagonize the secretory effect of VIP in rat ileum and colon.

作者信息

Bhaskar Rao M, O'Dorisio T M, Cataland S, George J M, Gaginella T S

出版信息

Peptides. 1984 Mar-Apr;5(2):291-4. doi: 10.1016/0196-9781(84)90221-3.

Abstract

Vasoactive intestinal polypeptide (VIP) induces intestinal secretion of water and electrolytes in experimental animals and man. We assessed the ability of angiotensin II (AII) and norepinephrine (NE) to block the secretion evoked by VIP, in vivo. Ileal and colonic segments in rats were perfused in situ for two hours with a physiological buffer containing [14C]-PEG-4000 as a volume marker. Saline (0.9% NaCl) was infused intravenously during the first hour and VIP or a combination of VIP plus AII or NE was infused during the second hour. All (0.7 ng/kg/min) alone enhanced water absorption significantly (p less than 0.01) in the ileum and an appreciable, although not a statistically significant, effect was observed in the colon. AII antagonized the secretory effects of VIP in the ileum as well as in the colon. Norepinephrine (5 micrograms/kg/min) also reversed the effect of VIP on the small intestine and colon. Although the mechanism by which AII antagonizes the secretory effects of VIP has not been identified, it is probable that AII promotes absorption, at least in part secondary to release of mucosal NE.

摘要

血管活性肠肽(VIP)可诱导实验动物和人体肠道分泌水和电解质。我们在体内评估了血管紧张素II(AII)和去甲肾上腺素(NE)阻断VIP诱发的分泌的能力。用含有[14C]-聚乙二醇-4000作为容积标记物的生理缓冲液对大鼠的回肠和结肠段进行原位灌注两小时。在第一个小时内静脉输注生理盐水(0.9%氯化钠),在第二个小时内输注VIP或VIP加AII或NE的组合。单独使用AII(0.7纳克/千克/分钟)可显著增强回肠的水吸收(p<0.01),在结肠中观察到了明显的效果,尽管在统计学上不显著。AII拮抗了VIP在回肠和结肠中的分泌作用。去甲肾上腺素(5微克/千克/分钟)也逆转了VIP对小肠和结肠的作用。虽然尚未确定AII拮抗VIP分泌作用的机制,但很可能AII促进吸收,至少部分是继发于黏膜NE的释放。

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