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大鼠早期和晚期尿毒症对尿素合成调节的相反作用。

Opposite effects on regulation of urea synthesis by early and late uraemia in rats.

作者信息

Nielsen Susanne Schouw, Grøfte Thorbjørn, Grønbaek Henning, Tygstrup Niels, Vilstrup Hendrik

机构信息

Department of Medicine V (Hepatology and Gastroenterology), Aarhus University Hospital, 44 Noerrebrogade, DK-8000 Aarhus C, Denmark.

出版信息

Clin Nutr. 2007 Apr;26(2):245-51. doi: 10.1016/j.clnu.2006.11.005. Epub 2007 Jan 23.

Abstract

BACKGROUND & AIMS: Acute and chronic kidney failure lead to catabolism with loss of lean body mass. Up-regulation of hepatic urea synthesis may play a role for the loss of body nitrogen and for the level of uraemia. The aims were to investigate the effects of early and late experimental renal failure on the regulation of hepatic urea synthesis and the expression of urea cycle enzyme genes in the liver.

METHODS

We examined the in vivo capacity of urea nitrogen synthesis, mRNA levels of urea cycle enzyme genes, and N-balances 6 days and 21 days after 5/6th partial nephrectomy in rats, and compared these data with pair- and free-fed control animals.

RESULTS

Compared with pair-fed animals, early uraemia halved the in vivo urea synthesis capacity and decreased urea gene expressions (P<0.05). In contrast, late uraemia up-regulated in vivo urea synthesis and expression of all urea genes (P<0.05), save that of the flux-generating enzyme carbamoyl phosphate synthetase. The N-balance in rats with early uraemia was markedly negative (P<0.05) and near zero in late uraemia.

CONCLUSIONS

Early uraemia down-regulated urea synthesis, so hepatic ureagenesis was not in itself involved in the negative N-balance. In contrast, late uraemia up-regulated urea synthesis, which probably contributed towards the reduced N-balance of this condition. These time-dependent, opposite effects on the uraemia-induced regulation of urea synthesis in vivo were not related to food restriction and probably mostly reflected regulation on gene level.

摘要

背景与目的

急性和慢性肾衰竭会导致分解代谢,伴有瘦体重的丢失。肝尿素合成上调可能在机体氮丢失和尿毒症水平方面发挥作用。本研究旨在探讨实验性早期和晚期肾衰竭对肝尿素合成调节及肝脏尿素循环酶基因表达的影响。

方法

我们检测了大鼠5/6肾切除术后6天和21天尿素氮合成的体内能力、尿素循环酶基因的mRNA水平以及氮平衡,并将这些数据与配对喂养和自由进食的对照动物进行比较。

结果

与配对喂养的动物相比,早期尿毒症使体内尿素合成能力减半,并降低了尿素基因表达(P<0.05)。相反,晚期尿毒症上调了体内尿素合成及所有尿素基因的表达(P<0.05),但通量生成酶氨甲酰磷酸合成酶的表达除外。早期尿毒症大鼠的氮平衡显著为负(P<0.05),晚期尿毒症时接近零。

结论

早期尿毒症下调尿素合成,因此肝尿素生成本身并不参与负氮平衡。相反,晚期尿毒症上调尿素合成,这可能导致了该状态下氮平衡的降低。这些对尿毒症诱导的体内尿素合成调节的时间依赖性相反效应与食物限制无关,可能主要反映了基因水平的调节。

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