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Effects of vasoactive intestinal polypeptide on intestinal absorption and blood flow.

机译:血管活性肠多肽对肠吸收和血流的影响。

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摘要

1. Intestinal absorption and blood flow in anaesthetized dogs was determined after I.V. infusion of vasoactive intestinal polypeptide (VIP) (1.75-175 ng/min) to determine the contribution of the cardiovascular changes to transport. 2. 22Na and 3H2O were utilized to determine the unidirectional fluxes of Na and H2O from saline perfused through the ileal lumen and the clearances of 3H2O were used to determine total and absorptive site blood flow. 3. Net Na and H2O absorption were reversed to secretion by VIP at 175 ng/min due to a significant decrease in unidirectional absorptive fluxes and smaller increases in secretory fluxes. 4. Arterial pressure and absorptive site blood flow were reduced in proportion to the changes in Na and H2O fluxes. 5. Total and absorptive site blood flow decreased and the blood flow resistances increased. 6. Prior treatment with guanethidine to suppress sympathetic effects did not greatly affect the responses to VIP. Prior treatment with atropine to suppress cholinergic effects inhibited most of the effects of VIP. 7. Absorptive site blood flow was linearly related to absorptive fluxes of Na and H2O but with different slopes for results from atropinized dogs as compared to those from dogs given VIP alone or VIP plus guanethidine. 8. It was concluded that VIP reduces gut absorption through a generalized cardiovascular effect and also through a mechanism which depends on the release of ACh by the gut.
机译:1.静脉注射后测定麻醉犬的肠吸收和血流量。输注血管活性肠多肽(VIP)(1.75-175 ng / min),以确定心血管变化对转运的贡献。 2.利用22Na和3H2O来确定通过回肠腔灌注的盐水中的Na和H2O的单向通量,并使用3H2O的清除率来确定总和吸收部位的血流。 3. VIP的净Na和H2O吸收在175 ng / min时被反向转化为分泌物,这是因为单向吸收通量显着降低,而分泌通量增加较小。 4.动脉压和吸收部位血流量与Na和H2O通量的变化成比例地降低。 5.总和吸收部位的血流量减少,血流阻力增加。 6.预先用胍乙啶治疗以抑制交感作用并没有很大地影响对VIP的反应。事先用阿托品治疗以抑制胆碱能作用抑制了VIP的大部分作用。 7.吸收部位的血流量与Na和H2O的吸收通量呈线性关系,但与单独给予VIP或VIP加胍乙啶的犬相比,萎缩性犬的结果具有不同的斜率。 8.结论是VIP通过普遍的心血管作用以及依赖于肠道释放ACh的机制来减少肠道吸收。

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