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急性肾小管坏死后氨基酸介导的肾磷脂生物合成刺激作用。

Amino acid-mediated stimulation of renal phospholipid biosynthesis after acute tubular necrosis.

作者信息

Toback F G, Teegarden D E, Havener L J

出版信息

Kidney Int. 1979 May;15(5):542-7. doi: 10.1038/ki.1979.69.

Abstract

The mechanism by which amino acid infusion stimulates membrane physpholipid biosynthesis during renal regeneration after mercuric-chloride-induced acute tubular necrosis was studied in the rat. Amino acids can act directly on regenerating renal tissue to enhance net phospholipid synthesis because preincubation of cortical slices with amino acids induced an increase in [14C]-choline incorporation into phospholipid without altering the rate of breakdown. This amino acid stimulation of phospholipid biosynthesis was studied further by measuring [14C]-choline accumulation and its sequential conversion to phosphorylcholine, cytidine diphosphocholine (CDP-choline), and phosphatidylcholine via the Kennedy pathway in regenerating renal tissue. [14C]-Choline accumulation was increased after amino acid infusion, compared to glucose infusion. There were also increments in the Vmax of the choline kinase reaction, which converts entering [14C]-choline into [14C]-phosphorylcholine, and of the cholinephosphotransferase reaction in which [14C]-CDP-choline is incorporated into [14C]-phosphatidylcholine, whereas the apparent Km of each reaction was unchanged. Thus, amino acids infused after tubular necrosis can act directly on regenerating renal cells to increase precursor availability and augment two reactions of the phospholipid biosynthetic pathway.

摘要

在大鼠中研究了在氯化汞诱导的急性肾小管坏死之后的肾再生过程中,氨基酸输注刺激膜磷脂生物合成的机制。氨基酸可直接作用于再生的肾组织以增强净磷脂合成,因为用氨基酸预孵育皮质切片会导致[14C]-胆碱掺入磷脂增加,而不会改变分解速率。通过测量[14C]-胆碱积累及其在再生肾组织中经由肯尼迪途径依次转化为磷酸胆碱、胞苷二磷酸胆碱(CDP-胆碱)和磷脂酰胆碱,进一步研究了氨基酸对磷脂生物合成的这种刺激作用。与输注葡萄糖相比,输注氨基酸后[14C]-胆碱积累增加。将进入的[14C]-胆碱转化为[14C]-磷酸胆碱的胆碱激酶反应以及将[14C]-CDP-胆碱掺入[14C]-磷脂酰胆碱的胆碱磷酸转移酶反应的Vmax也增加,而每个反应的表观Km不变。因此,肾小管坏死之后输注的氨基酸可直接作用于再生的肾细胞,以增加前体的可利用性并增强磷脂生物合成途径的两个反应。

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