Humphreys M H
Am J Physiol. 1976 Jun;230(6):1517-23. doi: 10.1152/ajplegacy.1976.230.6.1517.
The effect of furosemide on intestinal absorption of water and electrolytes was studied using segments of rat ileum perfused in vivo. Furosemide (1 mM) in the perfusion fluid reduced absorption of Na, Cl, and water by 50% from a balanced electrolyte solution without changing the transepithelial potential difference (PD). This effect was also observed in the absence of luminal glucose and was largely reversible. Substitution of all Na in perfusion fluid with choline produced secretion of Na and water and abolished Cl absorption; substitution of all Cl with SO4 reduced Na absorption to 20% of control values. Under both these conditions, furosemide had only trivial effects on electrolyte absorption and exerted no effect on PD. Measurements of unidirectional fluxes of Na and Cl showed that furosemide decreased net flux by reducing lumen-to-blood flux of these ions rather than increasing blood-to lumen flux. These results resemble those obtained in this tissue following exposure to acetazolamide, and suggest that furosemide inhibits a coupled, neutral process of NaCl transport from lumen to blood. Although this effect could be a result of carbonic anhydrase inhibition it more likely occurs from a separate action of furosemide on ileal transport.
利用在体灌注的大鼠回肠段研究了呋塞米对肠道水和电解质吸收的影响。灌注液中加入呋塞米(1 mM)可使平衡电解质溶液中的钠、氯和水的吸收减少50%,而不改变跨上皮电位差(PD)。在无管腔葡萄糖的情况下也观察到了这种效应,且该效应在很大程度上是可逆的。用胆碱替代灌注液中的所有钠会导致钠和水的分泌,并消除氯的吸收;用硫酸根替代所有氯会使钠的吸收降至对照值的20%。在这两种情况下,呋塞米对电解质吸收的影响都很小,对PD无影响。钠和氯的单向通量测量表明,呋塞米通过减少这些离子从管腔到血液的通量而不是增加从血液到管腔的通量来降低净通量。这些结果与该组织暴露于乙酰唑胺后获得的结果相似,提示呋塞米抑制了氯化钠从管腔到血液的耦联中性转运过程。虽然这种效应可能是碳酸酐酶抑制的结果,但更可能是呋塞米对回肠转运的独立作用所致。