肝损伤与脂质代谢:d-半乳糖胺诱导脂肪肝的性别差异。

Acta hepato-gastroenterologica Pub Date : 1979-04-01
R Kattermann, H Sirowej
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引用次数: 0

摘要

在给予3.48 mmol /kg (0.75 g/kg) d -半乳糖胺(Ga1N) 12、24和48小时后,研究了雄性和雌性大鼠的血脂变化和肝脏甘油三酯积累的时间过程。在ga1n诱导的肝损伤早期,血浆中甘油三酯、磷脂和总胆固醇的浓度下降,而在后期,这些值高于正常水平,特别是在雄性动物中。相反,葡萄糖浓度持续下降,而游离脂肪酸(FFA)水平上升到雌性动物正常水平的两倍。在整个实验过程中,雄性动物的fa值明显降低。与此一致的是,服用Ga1N 24小时后,雌性动物肝脏上的甘油三酯积累量为75 mg/g,而雄性动物平均仅为33 mg/g。在较低剂量的1.16和2.32 mmol/kg Ga1N下,雌性动物也出现了类似的脂肪浸润。由此可见,Ga1N给药后游离脂肪酸内流增加是脂肪浸润的主要原因,血浆游离脂肪酸浓度的性别差异解释了肝脏甘油三酯积累的净差异。脂肪肝发病机制的其他影响可能源于ga1n诱导的肝损伤后糖基化反应的紊乱和/或脂蛋白分泌和代谢的改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Liver injury and lipid metabolism: sex differences in the fatty liver induced by d-galactosamine.

The time-course of plasma lipid alterations and of triglyceride accumulation in the liver was investigated in male and female rats 12, 24 and 48 hours after treatment with 3.48 mmole/kg (0.75 g/kg) D-galactosamine (Ga1N). In the early stages of Ga1N-induced liver injury the concentrations of triglycerides, phospholipids and total cholesterol decreased, while in the later stages these values in the plasma increased above normal, especially in male animals. In contrast, glucose concentrations continually decreased, while free fatty acid (FFA) levels rose to twice those normal in female animals. Male animals had significantly lower FFA-values throughout the experiment. Consistently, the triglyceride accumulation on liver was 75 mg/g in female animals 24 hours after Ga1N administration, while male animals in the average showed only 33 mg/g triglycerides. Similar fatty infiltrations were obtained in female animals with the rather low doses of 1.16 and 2.32 mmol/kg Ga1N. It is concluded that the increase of FFA-influx after Ga1N administration is the main cause for fatty infiltration, the sex differences in the plasma FFA concentrations explaining the net differences in liver triglyceride accumulation. Additional effects in the pathogenesis of fatty liver might stem from disturbed glycosylation reactions and/or an altered secretion and metabolism of lipoproteins after Ga1N-induced liver injury.

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