Suzuki M, Almeida F A, Nussenzveig D R, Sawyer D, Maack T
Department of Physiology, Cornell University Medical College, New York, New York 10021.
Am J Physiol. 1987 Nov;253(5 Pt 2):F917-28. doi: 10.1152/ajprenal.1987.253.5.F917.
A new methodological approach was developed to study the relationship between specific binding and dose-response curves of the renal effects of atrial natriuretic factor (ANF) in isolated perfused rat kidneys (IK). IK were perfused with 125I-labeled and unlabeled ANF 1-28 (4 pM to 1 microM) to determine the following: 1) distribution, capacity (Cmax), and apparent affinity (S50) of specific binding of ANF 1-28 in cortex, outer medulla, and papilla and 2) dose-response curves of the effects of ANF 1-28 on renal hemodynamics and excretion of fluid and electrolytes. The kidney had a very high density of high-affinity binding sites for ANF. Cortex had greater than 90% of total binding sites (Cmax = 6.8 pmol/g tissue; S50 = 54 pM), whereas papilla had less than 2% of total binding sites with a 10-fold lower apparent affinity (S50 = 860 pM) than in cortex. ANF-induced increases in glomerular filtration rate and excretion of fluid and electrolytes were detectable at 10-100 pM and maximal effects occurred at 1-10 nM ANF. Below 1 nM there was no dissociation between the renal hemodynamic and natriuretic effects of ANF. There was a close agreement between dose-response and binding curves of ANF to cortex. Results demonstrate that binding site occupancy in kidney cortex and renal effects of ANF occur at near physiological concentrations of the hormone.
开发了一种新的方法来研究心房利钠因子(ANF)对离体灌注大鼠肾脏(IK)的肾脏效应的特异性结合与剂量反应曲线之间的关系。用125I标记和未标记的ANF 1-28(4 pM至1 microM)灌注IK,以确定以下内容:1)ANF 1-28在皮质、外髓和乳头中的特异性结合的分布、容量(Cmax)和表观亲和力(S50),以及2)ANF 1-28对肾脏血流动力学和液体及电解质排泄影响的剂量反应曲线。肾脏对ANF具有非常高的高亲和力结合位点密度。皮质占总结合位点的90%以上(Cmax = 6.8 pmol/g组织;S50 = 54 pM),而乳头占总结合位点的不到2%,其表观亲和力比皮质低10倍(S50 = 860 pM)。在10 - 100 pM时可检测到ANF诱导的肾小球滤过率以及液体和电解质排泄增加,最大效应出现在1 - 10 nM的ANF时。在1 nM以下,ANF的肾脏血流动力学和利钠效应之间没有分离。ANF与皮质的剂量反应曲线和结合曲线之间有密切的一致性。结果表明,在接近生理浓度的激素条件下,肾脏皮质中的结合位点占据和ANF的肾脏效应会发生。