Watanabe I, Goto F
Department of Anesthesiology, Takasaki National Hospital, Japan.
Jpn Circ J. 1994 Feb;58(2):136-42. doi: 10.1253/jcj.58.136.
Effects of alpha-human atrial natriuretic polypeptide (alpha-hANP) on renal function were studied in anesthetized dogs and isolated perfused rat kidneys. Two doses of alpha-hANP were used to determine whether renal hemodynamics or tubular reabsorption is tha major factor in the diuretic action of alpha hANP. The excretion rates of sodium (Na) and inorganic phosphate (PO4) were evaluated to determine the site of diuretic action in the renal tubule. In dogs that received the smaller dose of alpha-hANP (5 ng.kg-1.min-1) infused into the renal arteries without changes in systemic or renal hemodynamics, urine volume (UV) and urinary Na excretion (UNaV) increased significantly. Fractional excretion of Na (FENa) was increased, while fractional excretion of PO4 (FEpo4) was unchanged, following the infusion of alpha-hANP. The calculated fractional Na reabsorption in the distal tubule (DTRNa) during the infusion of alpha-hANP was significantly suppressed. In dogs that received the a larger dose of alpha-hANP (50 ng.kg-1.min-1), the glomerular filtration rate (GFR), UV, and FENa were increased and DTRNa was decreased. In isolated rat kidneys perfused at a constant pressure, a lower concentration of alpha-hANP (0.5 ng.ml-1) in the perfusate caused diuresis and increased Na and PO4 excretion without any renal hemodynamic alterations. A higher concentration of alpha-hANP (5 ng.ml-1) increased GFR, Na and PO4 excretion. Since PO4 reabsorption is believed to occur primarily in the renal proximal tubule, these findings suggest that the diuretic action of alpha-hANP in smaller doses in induced by direct action on renal distal nephron.(ABSTRACT TRUNCATED AT 250 WORDS)
在麻醉犬和离体灌注大鼠肾脏中研究了α-人心房利钠多肽(α-hANP)对肾功能的影响。使用两种剂量的α-hANP来确定肾血流动力学或肾小管重吸收是否是α-hANP利尿作用的主要因素。评估钠(Na)和无机磷酸盐(PO4)的排泄率以确定肾小管中利尿作用的部位。在接受较小剂量α-hANP(5 ng·kg-1·min-1)注入肾动脉且全身或肾血流动力学无变化的犬中,尿量(UV)和尿钠排泄(UNaV)显著增加。注入α-hANP后,钠分数排泄(FENa)增加,而磷酸盐分数排泄(FEpo4)不变。注入α-hANP期间,远端小管中计算出的钠重吸收分数(DTRNa)被显著抑制。在接受较大剂量α-hANP(50 ng·kg-1·min-1)的犬中,肾小球滤过率(GFR)、UV和FENa增加,DTRNa降低。在恒压灌注的离体大鼠肾脏中,灌注液中较低浓度的α-hANP(0.5 ng·ml-1)引起利尿并增加Na和PO4排泄,而无任何肾血流动力学改变。较高浓度的α-hANP(5 ng·ml-1)增加GFR、Na和PO4排泄。由于PO4重吸收主要发生在肾近端小管,这些发现表明较小剂量的α-hANP的利尿作用是由对肾远端肾单位的直接作用诱导的。(摘要截短于250字)