Hammarlund M, Paalzow L K
Biopharm Drug Dispos. 1985 Jan-Mar;6(1):9-21. doi: 10.1002/bdd.2510060103.
Furosemide was given to rats as five different i.v. bolus doses (2.5-100 mg kg-1), or as an i.v. infusion to a steady-state concentration in plasma of 14 micrograms ml-1. The urinary furosemide excretion rate (delta Ae/delta t) and the diuretic effect (volume of urine) were measured. A parallel shift in the excretion-response curve was seen as a fivefold increase in (delta Ae/delta t)50 [delta Ae/delta t) at half-maximal effect) between the i.v. bolus doses from 2.5 to 40 mg kg-1. The slope factor did not change. During infusion, a decrease in efficiency to 20 per cent of the initial value was seen. These results are indicative of an acute tolerance development to the diuretic effect of furosemide. Some intrarenal feedback inhibition mechanism might be involved, as the extracellular fluid volume seems to be of great importance to the effect obtained. The resulting effect can be compared with the influence of a competitive antagonist.
给大鼠静脉注射五种不同剂量的速尿(2.5 - 100毫克/千克),或静脉输注使其血浆稳态浓度达到14微克/毫升。测量尿速尿排泄率(ΔAe/Δt)和利尿作用(尿量)。静脉注射剂量从2.5毫克/千克增加到40毫克/千克时,排泄-反应曲线出现平行移动,最大效应一半时的排泄率(ΔAe/Δt)50增加了五倍,斜率因子不变。输注过程中,效率降至初始值的20%。这些结果表明对速尿的利尿作用出现了急性耐受性。可能涉及一些肾内反馈抑制机制,因为细胞外液量似乎对所获得的效应非常重要。所产生的效应可与竞争性拮抗剂的影响相比较。