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Do Elevated Plasma Vasoactive Intestinal Polypeptide (VIP) Levels Cause Small Intestinal Motor Disturbances in Humans?

机译:血浆血管活性肠多肽(VIP)水平升高会引起人类小肠运动障碍吗?

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摘要

Increased VIP plasma levels cause severe secretory diarrhea. Moreover, VIP is a major regulator of human intestinal motility. We hypothesized that VIP-mediated intestinal motility disturbances contribute to symptoms in elevated plasma VIP. Ten healthy volunteers were intubated twice with an orojejunal multilumen tube for duodenal manometry, jejunal perfusion of electrolyte and marker solution, and aspiration 10 and 40 cm more distally. All subjects randomly received intravenous infusion of saline and 300 pmol/kg * hr VIP for 5 hr. Results showed that VIP but not saline infusion induced net jejunal sodium secretion, watery diarrhea, and cardiovascular effects (P < 0.04). VIP did not alter intestinal motor activity or the mean duration of the interdigestive motility cycle or of phases I and II but nearly halved the duration of phase III (P = 0.0002). We conclude that increased plasma VIP markedly shortens human phase III activity without influencing other motility parameters. Hence, it is unlikely that VIP-mediated small intestinal motor disturbances cause symptoms in VIPOMA. Yet VIP may contribute to terminate phase III motility.
机译:VIP血浆水平升高会导致严重的分泌性腹泻。而且,VIP是人类肠道运动的主要调节剂。我们假设VIP介导的肠蠕动障碍导致血浆VIP升高的症状。十名健康志愿者用经口空肠多腔管插管两次,以进行十二指肠测压,对电解质和标记物溶液进行空肠灌注,并向远端抽吸10和40 cm。所有受试者随机接受生理盐水和300 pmol / kg *小时VIP的静脉输注5小时。结果表明,VIP注射但不注射生理盐水可导致空肠净钠分泌,水样腹泻和心血管疾病(P <0.04)。 VIP并没有改变肠动力活动或消化系统蠕动周期或I和II期的平均持续时间,但几乎使III期的持续时间减半(P = 0.0002)。我们得出结论,血浆VIP的增加明显缩短了人类III期的活动,而不会影响其他运动参数。因此,VIP介导的小肠运动障碍不太可能引起VIPOMA症状。 VIP可能有助于终止III期运动。

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