Brunette M G, Leclerc M
Maisonneuve-Rosemont Hospital, Research Center and University of Montreal, Quebec, Canada.
J Endocrinol. 2001 Aug;170(2):441-50. doi: 10.1677/joe.0.1700441.
Estrogens are widely used for contraception and osteoporosis prevention. The aim of the present study was to investigate the effect of 17 beta-estradiol on calcium (Ca(2+)) transport by the nephron luminal membranes, independently of any other Ca(2+)-regulating hormones. Proximal and distal tubules of rabbit kidneys were incubated with 17 beta-estradiol or the carrier for various periods of time, and the luminal membranes of these tubules were purified and vesiculated. Ca(2+) uptake by membrane vesicles was measured using the Millipore filtration technique. Incubation of proximal tubules with the hormone did not influence Ca(2+) uptake by the luminal membranes. In contrast, incubation of distal tubules with 10(-8) M 17 beta-estradiol for 30 min decreased the initial uptake of 0.5 mM Ca(2+) from 0.34+/-0.04 (s.e.m. ) to 0.17+/-0.04 pmol/microg per 5 s (P<0.05). In the presence of 100 mM Na(+), 0.5 mM Ca(2+) uptake was strongly diminished and the effect of 17 beta-estradiol disappeared (0.17+/-0.01 and 0.21+/-0.07 pmol/microg per 5 s in vesicles from the control and treated tubules). Direct incubation of the membranes with 17 beta-estradiol, however, failed to show any influence of the hormone on Ca(2+) transport. The action of 17 beta-estradiol was dose-dependent, with a half-maximal effect at approximately 10(-9) M. Ca(2+) uptake by the distal tubule membranes presents dual kinetics. 17 beta-Estradiol decreased the V(max) value of the high-affinity component from 0.42+/-0.02 to 0.31+/-0.03 pmol/microg per 10 s (P<0.02). In contrast with the effect of the hormone on Ca(2+) transport, estradiol increased Na(+) uptake by both the proximal and distal tubule luminal membranes. In conclusion, incubation of proximal and distal tubules with estrogen decreases Ca(2+) reabsorption by the high-affinity Ca(2+) channels of the distal luminal membranes, and enhances Na(+) transport by the membranes from proximal and distal nephrons.
雌激素被广泛用于避孕和预防骨质疏松症。本研究的目的是独立于任何其他钙调节激素,研究17β-雌二醇对肾单位管腔膜钙(Ca(2+))转运的影响。将兔肾近端和远端小管与17β-雌二醇或载体孵育不同时间,然后纯化这些小管的管腔膜并制成囊泡。使用密理博过滤技术测量膜囊泡对Ca(2+)的摄取。用激素孵育近端小管对管腔膜摄取Ca(2+)没有影响。相反,用10(-8) M 17β-雌二醇孵育远端小管30分钟,使0.5 mM Ca(2+)的初始摄取量从0.34±0.04(标准误)降至每5秒0.17±0.04 pmol/μg(P<0.05)。在存在100 mM Na(+)的情况下,0.5 mM Ca(2+)的摄取量大幅减少,17β-雌二醇的作用消失(对照和处理过的小管的囊泡中每5秒分别为0.17±0.01和0.21±0.07 pmol/μg)。然而,将膜与17β-雌二醇直接孵育未能显示该激素对Ca(2+)转运有任何影响。17β-雌二醇的作用呈剂量依赖性,在约10(-9) M时达到半数最大效应。远端小管膜对Ca(2+)的摄取呈现双重动力学。17β-雌二醇使高亲和力成分的V(max)值从每10秒0.42±0.02降至0.31±0.03 pmol/μg(P<0.02)。与激素对Ca(2+)转运的影响相反,雌二醇增加了近端和远端小管管腔膜对Na(+)的摄取。总之,用雌激素孵育近端和远端小管会降低远端管腔膜高亲和力Ca(2+)通道对Ca(2+)的重吸收,并增强近端和远端肾单位膜对Na(+)的转运。