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心房利钠因子与血管紧张素II在近端HCO3-重吸收中的相互作用。

Interaction of atrial natriuretic factor and angiotensin II in proximal HCO3- reabsorption.

作者信息

Gomes G N, Aires M M

机构信息

Department of Physiology, Escola Paulista de Medicina, Universidade de São Paulo, Brazil.

出版信息

Am J Physiol. 1992 Feb;262(2 Pt 2):F303-8. doi: 10.1152/ajprenal.1992.262.2.F303.

DOI:10.1152/ajprenal.1992.262.2.F303
PMID:1531734
Abstract

Bicarbonate reabsorption was evaluated by the acidification kinetics technique in middle proximal tubule in Munich-Wistar rats. Atrial natriuretic factor (ANF) and angiotensin II (ANG II) were infused into the jugular vein (ANF, 0.5 microgram.min-1.kg-1 after a prime of 10 micrograms/kg; ANG II, 20 ng.min-1.kg-1) or added to luminal or peritubular perfusion fluid (10(-6) M ANF; 10(-12) M ANG II). In the presence of ANF, in each condition, no significant differences in net HCO3- reabsorption or in acidification half time were observed compared with the control group. In the presence of ANG II, a significant increase in HCO3- reabsorption was observed, expressed by a fall in acidification half time from a mean of 4.75 +/- 0.20 (n = 86) to 2.47 +/- 0.18 s (n = 32) in systemically infused rats or to 2.30 +/- 0.15 s (n = 35) in luminally perfused tubules and from 4.57 +/- 0.32 (n = 44) to 2.04 +/- 0.10 s (n = 50) during capillary perfusion. However, when ANG II was systemically infused or perfused in lumen or in peritubular capillaries, addition of ANF to lumen or capillaries by perfusion or systemic infusion abolished the effects observed with ANG II alone. These studies confirm that ANG II stimulates proximal HCO3- reabsorption and show that ANF alone does not affect this process, but impairs the stimulation caused by ANG II.

摘要

采用酸化动力学技术,在慕尼黑-威斯塔大鼠的近端肾小管中段评估碳酸氢盐重吸收情况。将心房利钠因子(ANF)和血管紧张素II(ANG II)注入颈静脉(ANF,先静脉注射10微克/千克,随后以0.5微克·分钟-1·千克-1的速率输注;ANG II,以20纳克·分钟-1·千克-1的速率输注),或将其添加至管腔或肾小管周围灌注液中(10-6M ANF;10-12M ANG II)。在存在ANF的情况下,与对照组相比,在每种条件下,净HCO3-重吸收或酸化半衰期均未观察到显著差异。在存在ANG II的情况下,观察到HCO3-重吸收显著增加,表现为酸化半衰期缩短,在全身输注ANG II的大鼠中,酸化半衰期从平均4.75±0.20秒(n = 86)降至2.47±0.18秒(n = 32),在管腔灌注的肾小管中降至2.30±0.15秒(n = 35),在毛细血管灌注期间从4.57±0.32秒(n = 44)降至2.04±0.10秒(n = 50)。然而,当ANG II通过全身输注、管腔灌注或肾小管周围毛细血管灌注时,通过灌注或全身输注向管腔或毛细血管中添加ANF可消除单独使用ANG II时观察到的效应。这些研究证实ANG II刺激近端HCO3-重吸收,并表明单独的ANF不影响此过程,但会削弱ANG II引起的刺激作用。

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