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循环脂多糖结合蛋白(LBP)作为肥胖相关胰岛素抵抗的标志物。

Circulating lipopolysaccharide-binding protein (LBP) as a marker of obesity-related insulin resistance.

机构信息

Department of Diabetes, Endocrinology and Nutrition, Institut d'Investigació Biomèdica de Girona (IdIBGi), CIBEROBN (CB06/03/010) and Instituto de Salud Carlos III (ISCIII), Girona, Spain.

出版信息

Int J Obes (Lond). 2012 Nov;36(11):1442-9. doi: 10.1038/ijo.2011.256. Epub 2011 Dec 20.

Abstract

OBJECTIVE

Lipopolysaccharide-binding protein (LBP) is a 65-kDa acute-phase protein present in blood at high concentrations, known to be derived from the liver. We aimed to gain insights into the association of circulating LBP with insulin resistance in humans and mice. METHODS, DESIGN AND MEASUREMENTS: We studied the cross-sectional (n=222) and weight loss-induced (n=34) associations of LBP (enzyme-linked immunosorbent assay) with inflammatory and metabolic parameters (including minimal model-measured insulin sensitivity), and the effects of high-fat diet (HFD), metformin and genetic insulin sensitization (glucagon-like peptide 1 receptor knockout model) in mice.

RESULTS

Circulating LBP concentration was significantly increased in subjects with type 2 diabetes and dramatically increased in subjects with morbid obesity. LBP was significantly associated with insulin sensitivity and different inflammatory markers and decreased after weight loss (22.2 ± 5.8 vs 16.2 ± 9.3 μg ml(-1), P<0.0001) in association with changes in body mass index and insulin sensitivity. Circulating LBP concentration was increased in HFD mice, whereas decreased in glucagon-like peptide 1 receptor knockout mice (significantly more insulin sensitive than wild-type mice) and after metformin administration.

CONCLUSION

LBP is an inflammatory marker associated with obesity-related insulin resistance.

摘要

目的

脂多糖结合蛋白(LBP)是一种 65kDa 的急性期蛋白,在血液中以高浓度存在,已知来源于肝脏。我们旨在深入了解循环 LBP 与人类和小鼠胰岛素抵抗的关系。

方法、设计和测量:我们研究了 LBP(酶联免疫吸附测定)与炎症和代谢参数(包括最小模型测量的胰岛素敏感性)的横断面(n=222)和减肥诱导(n=34)的相关性,以及高脂肪饮食(HFD)、二甲双胍和遗传胰岛素敏感性(胰高血糖素样肽 1 受体敲除模型)在小鼠中的作用。

结果

2 型糖尿病患者的循环 LBP 浓度显著升高,病态肥胖患者的循环 LBP 浓度显著升高。LBP 与胰岛素敏感性和不同的炎症标志物显著相关,并且在与体重指数和胰岛素敏感性变化相关的体重减轻后(22.2±5.8 vs 16.2±9.3μg/ml,P<0.0001)降低。HFD 小鼠的循环 LBP 浓度升高,而胰高血糖素样肽 1 受体敲除小鼠(比野生型小鼠胰岛素敏感性显著更高)和二甲双胍给药后降低。

结论

LBP 是一种与肥胖相关的胰岛素抵抗相关的炎症标志物。

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