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氨氯吡咪、呋塞米、布美他尼和氨苯蝶啶对猪胰腺碳酸氢钠分泌无作用。

Lack of effect of amiloride, furosemide, bumetanide and triamterene on pancreatic NaHCO3 secretion in pigs.

作者信息

Grotmol T, Buanes T, Brørs O, Raeder M G

出版信息

Acta Physiol Scand. 1986 Apr;126(4):593-600. doi: 10.1111/j.1748-1716.1986.tb07860.x.

Abstract

This study examines the effects of the Na entry blockers amiloride, furosemide, bumetanide and triamterene on pancreatic NaHCO3 secretion. The purpose of the study was to elucidate whether Na flux through a Na-H-antiport, a Na,K,Cl-symport or a Na-K(H)-antiport respectively, may be rate limiting for pancreatic NaHCO3 secretion. The effect of each drug on secretion was tested in four groups of six anaesthetized pigs (20-25 kg body wt) during supramaximal, intravenous secretin infusion (3.0 CU kg-1 body wt. h-1), following laparotomy and cannulation of the pancreatic duct. Secretion was measured over a wide range of arterial pH values, both before and after drug administration in each animal. Pancreatic NaHCO3 secretion averaged 268 (219-308) mumol min-1 at physiological arterial pH 7.40 in the control period. Neither amiloride (90 mg kg-1 body wt), furosemide (10 mg kg-1 body wt), bumetanide (0.6 mg kg-1 body wt) nor triamterene (25 mg kg-1 body wt) affected the rate of secretin-dependent NaHCO3 secretion or the relation between NaHCO3 secretion and arterial pH. It is concluded that Na flux through neither a Na-H-antiport, a Na,K,Cl-symport nor a Na-K(H)-antiport appears to be rate limiting for pancreatic secretion of NaHCO3.

摘要

本研究考察了钠进入阻滞剂氨氯吡咪、呋塞米、布美他尼和氨苯蝶啶对胰腺碳酸氢钠分泌的影响。本研究的目的是阐明分别通过钠-氢反向转运体、钠-钾-氯同向转运体或钠-钾(氢)反向转运体的钠通量是否可能是胰腺碳酸氢钠分泌的限速因素。在剖腹手术并对胰管插管后,于超最大剂量静脉输注促胰液素(3.0 CU kg-1体重·小时-1)期间,在四组六头麻醉猪(体重20 - 25 kg)中测试了每种药物对分泌的影响。在每只动物给药前后,在很宽的动脉pH值范围内测量分泌情况。在对照期,生理动脉pH值7.40时,胰腺碳酸氢钠分泌平均为268(219 - 308)μmol min-1。氨氯吡咪(90 mg kg-1体重)、呋塞米(10 mg kg-1体重)、布美他尼(0.6 mg kg-1体重)或氨苯蝶啶(25 mg kg-1体重)均未影响促胰液素依赖性碳酸氢钠分泌速率或碳酸氢钠分泌与动脉pH之间的关系。得出的结论是,通过钠-氢反向转运体、钠-钾-氯同向转运体或钠-钾(氢)反向转运体的钠通量似乎均不是胰腺碳酸氢钠分泌的限速因素。

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