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补充半胱氨酸并减少全肠外营养诱导的断奶大鼠肝脏脂质积累。

Cysteine supplementation and reduction of total parenteral nutrition-induced hepatic lipid accumulation in the weanling rat.

作者信息

Narkewicz M R, Caldwell S, Jones G

机构信息

Department of Pediatrics, University of Colorado School of Medicine, Denver, USA.

出版信息

J Pediatr Gastroenterol Nutr. 1995 Jul;21(1):18-24. doi: 10.1097/00005176-199507000-00003.

DOI:10.1097/00005176-199507000-00003
PMID:8576809
Abstract

Total parenteral nutrition (TPN)-induced hepatic steatosis is the most common complication of TPN administration to humans. The mechanism of TPN-induced hepatic steatosis has not been studied in young mammals. The goal of this study was to determine the mechanism of TPN-induced hepatic steatosis in the weanling rat and the effect of supplementation of TPN with choline and/or cysteine on TPN-induced hepatic steatosis. In the weanling rat, we investigated the effect of TPN administration on histologic hepatic steatosis, total hepatic lipid, hepatic acetyl-CoA-carboxylase (ACC--the rate limiting enzyme in fatty acid synthesis) specific activity, and total plasma lipids. TPN administration resulted in a threefold increase in hepatic lipid as compared with control and sham animals (TPN 138 +/- 12 mg/g liver versus control 57 +/- 1), an increase in histologic steatosis (TPN 3.7 versus control 1.3), and a decline in total plasma lipid (TPN 2.1 +/- 0.3 g/L versus control 4.1 +/- 0.3). TPN-induced hepatic steatosis in the weanling rat was not associated with an increase in ACC specific activity (TPN 2.10 +/- 0.33 nmol/min/mg protein versus control 2.85 +/- 0.23). Supplementation of the TPN with choline (15 mg/day) did not significantly lessen hepatic steatosis; however, supplementation of TPN with cysteine (2.5 mg/day) or with cysteine and choline did result in a significant lessening of hepatic lipid content and of histologic steatosis and a normalization of total plasma lipid.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

全胃肠外营养(TPN)诱导的肝脂肪变性是对人类进行TPN治疗时最常见的并发症。TPN诱导肝脂肪变性的机制在幼年哺乳动物中尚未得到研究。本研究的目的是确定断乳大鼠中TPN诱导肝脂肪变性的机制,以及在TPN中补充胆碱和/或半胱氨酸对TPN诱导的肝脂肪变性的影响。在断乳大鼠中,我们研究了TPN给药对肝脏组织学脂肪变性、肝脏总脂质、肝脏乙酰辅酶A羧化酶(ACC,脂肪酸合成中的限速酶)比活性以及血浆总脂质的影响。与对照组和假手术动物相比,TPN给药导致肝脏脂质增加了两倍(TPN组为138±12mg/g肝脏,对照组为57±1),组织学脂肪变性增加(TPN组为3.7,对照组为1.3),血浆总脂质下降(TPN组为2.1±0.3g/L,对照组为4.1±0.3)。断乳大鼠中TPN诱导的肝脂肪变性与ACC比活性增加无关(TPN组为2.10±0.33nmol/min/mg蛋白,对照组为2.85±0.23)。在TPN中补充胆碱(15mg/天)并没有显著减轻肝脂肪变性;然而,在TPN中补充半胱氨酸(2.5mg/天)或同时补充半胱氨酸和胆碱确实导致肝脏脂质含量和组织学脂肪变性显著减轻,以及血浆总脂质恢复正常。(摘要截短于250字)

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