Dennhardt R, Lingelbach B, Haberich F J
Gut. 1979 Feb;20(2):107-13. doi: 10.1136/gut.20.2.107.
Experiments were carried out in different segments of the intestine of unanaesthetised rats to assess the effect of vasopressin on intestinal absorptive processes. The following data were observed. (1) Within a physiological range of doses (Aziz, 1969), ADH diminished the net sodium absorption mainly by reducing the unidirectional sodium influx, whereas the behaviour of the efflux was not uniform. (2) The unidirectional volume fluxes showed the same behaviour as did the sodium fluxes. (3) ADH produced an oral-aboral gradient (jejunum greater than ileum greater than colon). (4) ADH did not significantly change the transfer of actively transported sugars; it did influence, however, passively transported substances. (5) During the intravenous application of ADH, a substance was secreted into the perfusion solution which diminished the absorption of volume and electrolytes. (6) Cyclic AMP acted on intestinal absorption in the same way as did ADH. In view of these results two mutually independent transport pathways for sodium and water are supposed, one of which is influenced by ADH or cAMP. Based on a two membrane model, an ADH mechanism is discussed: the permeability of the luminal membrane system is enhanced in the presence of vasopressin.
在未麻醉大鼠的不同肠段进行实验,以评估血管加压素对肠道吸收过程的影响。观察到以下数据:(1) 在生理剂量范围内(阿齐兹,1969年),抗利尿激素主要通过减少单向钠内流来降低钠的净吸收,而外流的表现并不一致。(2) 单向体积通量与钠通量表现出相同的行为。(3) 抗利尿激素产生了一个口-肛梯度(空肠大于回肠大于结肠)。(4) 抗利尿激素并未显著改变主动转运糖的转运;然而,它确实影响了被动转运的物质。(5) 在静脉注射抗利尿激素期间,一种物质分泌到灌注液中,该物质减少了体积和电解质的吸收。(6) 环磷酸腺苷对肠道吸收的作用与抗利尿激素相同。鉴于这些结果,推测存在两条相互独立的钠和水转运途径,其中一条受抗利尿激素或环磷酸腺苷影响。基于双膜模型,讨论了一种抗利尿激素机制:在血管加压素存在的情况下,腔膜系统的通透性增强。