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蛋氨酸-胆碱缺乏性脂肪性肝炎饮食模型不表现出胰岛素抵抗。

The methionine-choline deficient dietary model of steatohepatitis does not exhibit insulin resistance.

作者信息

Rinella Mary E, Green Richard M

机构信息

Northwestern University Feinberg School of Medicine, Division of Hepatology, 303 E. Chicago Ave, Searle 10-567, Chicago, IL 60611, USA.

出版信息

J Hepatol. 2004 Jan;40(1):47-51. doi: 10.1016/j.jhep.2003.09.020.

Abstract

BACKGROUND/AIMS: Non-alcoholic steatohepatitis is an important disease whose pathophysiology remains incompletely understood, although in humans a strong association with insulin resistance exists. Mice fed a methionine-choline deficient (MCD) diet develop steatohepatitis, however the influence of insulin in this model is unknown.

METHODS

Male FVB/NJ mice were fed the MCD, MCD control or chow diet for 10 or 28 days. Fasting glucose, ALT, triglyceride and insulin was measured. Glucose tolerance tests (GTT) and insulin tolerance tests (ITT) were performed followed by quantitative insulin sensitivity check index (QUICKI) determination.

RESULTS

ALT levels were significantly higher in the MCD group. Fasting glucose was 81+/-5 mg/dl in MCD diet fed mice, compared to MCD controls (196+/-46 mg/dl) and chow (199+/-15 mg/dl) (P<0.0001). During GTT and ITT, the effect of glucose administration on blood glucose was dampened, and the insulin effect more pronounced in the MCD group (P=0.026 and P<0.001). QUICKI in MCD fed mice was significantly higher than in the chow fed mice.

CONCLUSIONS

GTT, ITT and QUICKI confirmed the absence of insulin resistance in the MCD fed mice. This model causes fibrosing steatohepatitis and may help delineate the non-insulin resistant mechanisms involved in human steatohepatitis.

摘要

背景/目的:非酒精性脂肪性肝炎是一种重要疾病,尽管在人类中它与胰岛素抵抗存在密切关联,但其病理生理学仍未完全明确。喂食蛋氨酸-胆碱缺乏(MCD)饮食的小鼠会发生脂肪性肝炎,然而胰岛素在该模型中的影响尚不清楚。

方法

将雄性FVB/NJ小鼠分别喂食MCD饮食、MCD对照饮食或普通饮食10天或28天。测量空腹血糖、谷丙转氨酶(ALT)、甘油三酯和胰岛素水平。进行葡萄糖耐量试验(GTT)和胰岛素耐量试验(ITT),随后测定定量胰岛素敏感性检查指数(QUICKI)。

结果

MCD组的ALT水平显著更高。喂食MCD饮食的小鼠空腹血糖为81±5mg/dl,而MCD对照组为(196±46mg/dl),普通饮食组为(199±15mg/dl)(P<0.000l)。在GTT和ITT期间,MCD组给予葡萄糖后对血糖的影响减弱,而胰岛素的作用更明显(P=0.026和P<0.001)。喂食MCD饮食的小鼠的QUICKI显著高于喂食普通饮食的小鼠。

结论

GTT、ITT和QUICKI证实喂食MCD饮食的小鼠不存在胰岛素抵抗。该模型可导致纤维化脂肪性肝炎,可能有助于阐明人类脂肪性肝炎中涉及的非胰岛素抵抗机制。

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