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兔肾皮质切片对对氨基马尿酸盐蓄积的代谢调节研究。

Investigations on metabolic modulation of p-aminohippurate accumulation by rabbit renal cortical slices.

作者信息

Hewitt W R, Clark R L, Hook J B

出版信息

J Pharmacol Exp Ther. 1976 Dec;199(3):498-509.

PMID:11338
Abstract

Preparation and incubation of renal cortical slices from adult, female, New Zealand white rabbit depleted tissue citrate concentration. Acetate (10.0 mM) in the incubation significantly increased slice citrate concentration and p-aminohippurate (PAH) accumulation. Physiological concentrations of citrate increased PAH accumulation and final medium pH. increasing concentrations of citrate produced a biphasic effect on PAH accumulation. These data suggested that citrate may act as an intracellular modulator of organic anion transport. This hypothesis was tested with other stimulators of PAH accumulation. Physiological concentrations of alpha-ketoglutarate or succinate increased slice accumulation of PAH. Higher concentrations of either substrate significantly inhibited PAH accumulation. Final medium pH increased with increased medium concentration of both substrates. alpha-Ketoglutarate (0.5 mM) increased PAH accumulation but had no effect on slice citrate concentration. Glucose did not alter either PAH accumulation or slice citrate concentration. Slices incubated without substrate were depleted of citrate but not of alpha-ketoglutarate. Acetate (1.0 mM) significantly increased slice concentration of both alpha-ketoglutarate and citrate. These data suggested that organic anion transport could be modulated by several metabolic intermediates acting through similar but separate mechanisms.

摘要

成年雌性新西兰白兔肾皮质切片的制备与孵育,组织柠檬酸盐浓度降低。孵育液中的乙酸盐(10.0 mM)显著提高了切片柠檬酸盐浓度和对氨基马尿酸(PAH)蓄积。生理浓度的柠檬酸盐增加了PAH蓄积和最终培养基pH值。柠檬酸盐浓度增加对PAH蓄积产生双相效应。这些数据表明柠檬酸盐可能作为有机阴离子转运的细胞内调节剂。用其他PAH蓄积刺激剂对该假设进行了检验。生理浓度的α-酮戊二酸或琥珀酸盐增加了切片PAH蓄积。两种底物的较高浓度均显著抑制PAH蓄积。随着培养基中两种底物浓度增加,最终培养基pH值升高。α-酮戊二酸(0.5 mM)增加了PAH蓄积,但对切片柠檬酸盐浓度无影响。葡萄糖未改变PAH蓄积或切片柠檬酸盐浓度。在无底物条件下孵育的切片柠檬酸盐耗尽,但α-酮戊二酸未耗尽。乙酸盐(1.0 mM)显著提高了α-酮戊二酸和柠檬酸盐的切片浓度。这些数据表明有机阴离子转运可被几种通过相似但不同机制起作用的代谢中间产物调节。

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