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肝损伤与脂质代谢:d-半乳糖胺诱导的脂肪肝中的性别差异

Liver injury and lipid metabolism: sex differences in the fatty liver induced by d-galactosamine.

作者信息

Kattermann R, Sirowej H

出版信息

Acta Hepatogastroenterol (Stuttg). 1979 Apr;26(2):112-21.

PMID:463486
Abstract

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.

摘要

在用3.48毫摩尔/千克(0.75克/千克)D-半乳糖胺(GalN)处理后的12、24和48小时,对雄性和雌性大鼠血浆脂质变化及肝脏中甘油三酯蓄积的时间进程进行了研究。在GalN诱导的肝损伤早期,甘油三酯、磷脂和总胆固醇浓度降低,而在后期,血浆中的这些值高于正常水平,尤其是在雄性动物中。相比之下,葡萄糖浓度持续降低,而雌性动物中游离脂肪酸(FFA)水平升至正常水平的两倍。在整个实验过程中,雄性动物的FFA值显著较低。一致的是,在给予GalN 24小时后,雌性动物肝脏中的甘油三酯蓄积量为75毫克/克,而雄性动物平均仅显示33毫克/克甘油三酯。用1.16和2.32毫摩尔/千克的低剂量GalN处理雌性动物也获得了类似的脂肪浸润。结论是,给予GalN后FFA流入增加是脂肪浸润的主要原因,血浆FFA浓度的性别差异解释了肝脏甘油三酯蓄积的净差异。脂肪肝发病机制中的其他影响可能源于糖基化反应紊乱和/或GalN诱导的肝损伤后脂蛋白分泌和代谢改变。

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