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在低密度脂蛋白受体(LDL-R)基因敲除小鼠的西式饮食中添加液态果糖,会诱导肝脏炎症和纤维化标志物的产生,且在胰岛素刺激后不会破坏胰岛素受体信号传导。

The Addition of Liquid Fructose to a Western-Type Diet in LDL-R Mice Induces Liver Inflammation and Fibrogenesis Markers without Disrupting Insulin Receptor Signalling after an Insulin Challenge.

作者信息

Sangüesa Gemma, Baena Miguel, Hutter Natalia, Montañés José Carlos, Sánchez Rosa María, Roglans Núria, Laguna Juan Carlos, Alegret Marta

机构信息

Department of Pharmacology, Toxicology and Therapeutic Chemistry, School of Pharmacy and Food Sciences, University of Barcelona, 08028 Barcelona, Spain.

Institute of Biomedicine, University of Barcelona, 08028 Barcelona, Spain.

出版信息

Nutrients. 2017 Mar 15;9(3):278. doi: 10.3390/nu9030278.

Abstract

A high consumption of fat and simple sugars, especially fructose, has been related to the development of insulin resistance, but the mechanisms involved in the effects of these nutrients are not fully understood. This study investigates the effects of a Western-type diet and liquid fructose supplementation, alone and combined, on insulin signalling and inflammation in low-density lipoprotein (LDL) receptor-deficient mice (LDL-R). LDL-R mice were fed chow or Western diet ±15% fructose solution for 12 weeks. Plasma glucose and insulin, and the expression of genes related to inflammation in the liver and visceral white adipose tissue (vWAT), were analysed. V-akt murine thymoma viral oncogene homolog-2 (Akt) activation was measured in the liver of the mice after a single injection of saline or insulin. None of the dietary interventions caused inflammation in vWAT, whereas the Western diet induced hepatic inflammation, which was further enhanced by liquid fructose, leading also to a significant increase in fibrogenesis markers. However, there was no change in plasma glucose or insulin, or insulin-induced Akt phosphorylation. In conclusion, hepatic inflammation and fibrogenesis markers induced by a Western diet supplemented with liquid fructose in LDL-R mice are not associated with a significant impairment of hepatic insulin signalling.

摘要

高脂肪和单糖,尤其是果糖的高摄入量,与胰岛素抵抗的发展有关,但这些营养素作用的相关机制尚未完全明确。本研究调查了西式饮食和液体果糖补充剂单独及联合使用对低密度脂蛋白(LDL)受体缺陷小鼠(LDL-R)胰岛素信号传导和炎症的影响。给LDL-R小鼠喂食普通饲料或西式饮食±15%果糖溶液,持续12周。分析血浆葡萄糖和胰岛素,以及肝脏和内脏白色脂肪组织(vWAT)中与炎症相关基因的表达。在单次注射生理盐水或胰岛素后,测定小鼠肝脏中V-akt小鼠胸腺瘤病毒癌基因同源物2(Akt)的激活情况。没有一种饮食干预导致vWAT发生炎症,而西式饮食诱导肝脏炎症,液体果糖进一步加剧了这种炎症,还导致纤维化标志物显著增加。然而,血浆葡萄糖、胰岛素或胰岛素诱导的Akt磷酸化没有变化。总之,在LDL-R小鼠中,补充液体果糖的西式饮食诱导的肝脏炎症和纤维化标志物与肝脏胰岛素信号传导的显著受损无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59bf/5372941/b8ba823f8c0f/nutrients-09-00278-g001.jpg

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