Renal synthesis, degradation and active transport of aliphatic acyl amino acids relationship to p-aminohippurate transport.
Renal synthesis, degradation and active transport of aliphatic acyl amino acids relationship to p-aminohippurate transport.
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脂肪族酰基氨基酸的肾脏合成、降解和主动转运与对氨基马尿酸转运的关系。
DOI:
10.1152/ajplegacy.1955.182.3.537
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发表时间:
1955
期刊:
影响因子:
--
通讯作者:
J. Taggart
中科院分区:
文献类型:
--
作者:
D. Schachter;J. Manis;J. Taggart
OTH in vitro and in z&o experiments B have shown that low concentrations of various metabolic intermediates exert a profound influence on the mechanism responsible for the tubular excretion of p-aminohippurate (PAH). Acetate and its precursors, lactate and pyruvate, increase the rate of PAH transport by 30-IOO%, or more, in the rabbit (I), dog (2) and man (3). In contrast, PAH transport is depressed markedly by low concentrations of the dicarboxylic acids of the citric acid cycle, by fatty acids of intermediate carbon chain length (Ce-CIJ, and by certain amino acids, viz. L-alanine and L-glutamate (I). Neither the augmentation or depression of PAH transport by the various substrates appears to be related directly to effects on cellular respiration. Recent studies in this laboratory have been concerned with the biosynthesis of hippurate and other N-acylglycines (4, 5). The acyl thio esters of coenzyme A (R-CO-S-CoA) have been established as the energy-rich intermediates in acylglycine synthesis, as shown in the following equations: