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肝脏硬脂酰辅酶A去饱和酶1活性降低与肥胖人群的脂肪肝和胰岛素抵抗相关。

Low hepatic stearoyl-CoA desaturase 1 activity is associated with fatty liver and insulin resistance in obese humans.

作者信息

Stefan N, Peter A, Cegan A, Staiger H, Machann J, Schick F, Claussen C D, Fritsche A, Häring H-U, Schleicher E

机构信息

Department of Internal Medicine, Division of Endocrinology, Diabetology, Vascular Medicine, Nephrology and Clinical Chemistry, University of Tübingen, Otfried-Müller-Str. 10, 72076 Tübingen, Germany.

出版信息

Diabetologia. 2008 Apr;51(4):648-56. doi: 10.1007/s00125-008-0938-7. Epub 2008 Feb 20.

Abstract

AIMS/HYPOTHESIS: Stearoyl-CoA desaturase 1 (SCD1) is the rate-limiting enzyme in monounsaturated fatty acid synthesis. It is imperative for the assembly of VLDL particles, which transport triacylglycerol (TG) from liver to adipose tissue and other sites. We aimed to determine the role of hepatic SCD1 activity in human glucose and lipid metabolism.

METHODS

We studied 54 people participating in a lifestyle intervention programme with diet modification and increased physical activity. Insulin sensitivity was determined during a euglycaemic-hyperinsulinaemic clamp and estimated from an OGTT. Liver fat was quantified by (1)H-magnetic resonance spectroscopy at baseline and after 9 months of intervention. The pattern of fatty acids in serum VLDL-TGs was determined by ultracentrifugation followed by thin layer and gas chromatography, with the 18:1 n-9: 18:0 ratio providing an index of hepatic SCD1 activity.

RESULTS

The hepatic SCD1 activity index correlated negatively with liver fat (r= -0.29, p=0.04) and positively with insulin sensitivity, both OGTT-derived (r=0.42, p=0.003) and clamp-derived (r=0.27, p=0.07). These correlations depended on overall adiposity. They were absent in leaner participants (n=27, liver fat: p=0.34, insulin sensitivity [OGTT]: p=0.75, insulin sensitivity [clamp]: p=0.24), but were strong in obese individuals (n=27, p=0.004, p=0.0002 and p=0.006, respectively). Furthermore, during intervention a high SCD1 activity index at baseline predicted a decrease in liver fat only in obese participants (r= -0.46, p=0.02).

CONCLUSIONS/INTERPRETATION: Our data suggest that high hepatic SCD1 activity may regulate fat accumulation in the liver and possibly protects from insulin resistance in obesity.

摘要

目的/假设:硬脂酰辅酶A去饱和酶1(SCD1)是单不饱和脂肪酸合成中的限速酶。它对于极低密度脂蛋白(VLDL)颗粒的组装至关重要,VLDL负责将三酰甘油(TG)从肝脏转运至脂肪组织及其他部位。我们旨在确定肝脏SCD1活性在人体葡萄糖和脂质代谢中的作用。

方法

我们研究了54名参与生活方式干预项目的人员,这些项目包括饮食调整和增加体育活动。在正常血糖-高胰岛素钳夹期间测定胰岛素敏感性,并通过口服葡萄糖耐量试验(OGTT)进行评估。在基线和干预9个月后,通过氢磁共振波谱法对肝脏脂肪进行定量。通过超速离心,随后进行薄层色谱和气相色谱法,测定血清VLDL-TG中的脂肪酸模式,18:1 n-9与18:0的比值可作为肝脏SCD1活性的指标。

结果

肝脏SCD1活性指数与肝脏脂肪呈负相关(r = -0.29,p = 0.04),与胰岛素敏感性呈正相关,无论是来自OGTT(r = 0.42,p = 0.003)还是钳夹试验(r = 0.27,p = 0.07)。这些相关性取决于总体肥胖程度。在较瘦的参与者中不存在这些相关性(n = 27,肝脏脂肪:p = 0.34,胰岛素敏感性[OGTT]:p = 0.75,胰岛素敏感性[钳夹试验]:p = 0.24),但在肥胖个体中相关性很强(n = 27,分别为p = 0.004、p = 0.0002和p = 0.006)。此外,在干预期间,基线时高SCD1活性指数仅在肥胖参与者中预测肝脏脂肪减少(r = -0.46,p = 0.02)。

结论/解读:我们的数据表明,肝脏SCD1高活性可能调节肝脏中的脂肪积累,并可能在肥胖中预防胰岛素抵抗。

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