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Ribonucleic acid synthesis in the renal cortex at the initiation of compensatory growth.

机译:代偿性生长开始时肾皮质中的核糖核酸合成。

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摘要

The mechanisms responsible for the increase in RNA per cell during the first 48h of renal compensatory growth were studied in the renal cortex. Unilaterally nephrectomized, sham-operated or non-operated rats were used. Incorporation into RNA of labelled precursors was studied in vivo and in vitro. Sham-operation produced significant changes in precursor incorporation, absolute amounts of UTP and RNA, and the rate of RNA synthesis. At 6h after surgery, the amount of RNA decreased in sham-operated controls, whereas that in growing cortex remained unchanged. Incorporation into RNA in vivo was greater in the growing cortex, although the rate of RNA synthesis was not increased. At 24h, precursor incorporation into RNA and UTP and RNA synthesis were all increased in the growing cortex. In contrast with results obtained in vivo, slices of growing cortex incorporated less labelled precursor into RNA than did cortex slices from sham-operated controls, from 3 to 48h. Maximal differences were found from 6 to 24h. An attempt was made to equalize endogenous precursor pool sizes by increasing the concentration of unlabelled uridine in the media; incorporation differences were narrowed significantly. Serum from nephrectomized animals did not increase precursor incorporation into RNA in vitro. An increase in RNA synthesis is an important factor in RNA accretion in the renal cortex beyond 12h of compensatory growth. This is accompanied by increased UTP content and preceded by expansion of other pools. The amount of labelled precursor incorporated into RNA is greatly influenced by its delivery rate to the growing kidney in vivo and by intracellular dilution of expanded precursor pools in vitro.
机译:在肾皮质中研究了在肾脏代偿性生长的前48小时内每个细胞RNA升高的机制。使用单侧肾切除,假手术或非手术大鼠。在体内和体外研究了将标记的前体掺入RNA。假手术在前体掺入,UTP和RNA的绝对量以及RNA合成速率方面产生了重大变化。手术后6小时,假手术对照组的RNA数量减少,而皮质生长的RNA数量保持不变。尽管没有增加RNA合成的速度,但在生长的皮质中体内掺入RNA的比例更高。在第24小时,在皮层中,前体掺入RNA和UTP以及RNA合成均增加。与在体内获得的结果相反,在3至48小时内,生长的皮质切片将比假手术对照的皮质切片掺入的标记前体更少。从6到24小时发现最大差异。尝试通过增加培养基中未标记尿苷的浓度来平衡内源性前体库的大小;掺入差异明显缩小。肾切除动物的血清在体外不增加前体掺入RNA的能力。 RNA合成的增加是补偿性生长超过12小时后肾皮质RNA积聚的重要因素。这伴随着UTP内容的增加以及其他池的扩展。掺入RNA中的标记前体的量在很大程度上受其向体内不断增长的肾脏的递送速率和体外扩增的前体库的细胞内稀释的影响。

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