Hepatic oleate regulates liver stress response partially through PGC-1α during high-carbohydrate feeding

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• 作者：Xueqing Liu¹ ; ^&dagger ; ; Maggie S. Burhans² ; ^&dagger ; ; Matthew T. Flowers¹ ; James M. Ntambi¹ ; ² ; ^{ntambi@biochem.wisc.edu" class="auth_mail" title="E-mail the corresponding author}
• 关键词：ER ; endoplasmic reticulum ; TG ; triglycerides ; CE ; cholesterol esters ; PL ; phospholipids ; FFA ; free fatty acids ; SFA ; saturated fatty acids ; MUFA ; monounsaturated fatty acids ; SCD ; stearoyl-CoA desaturase ; GKO ; global knockout ; HSVLF ; high-sucrose very low-fat ; LKO ; liver-specific knockout ; GLS5 ; GKO liver-specific SCD5 ; GLS3 ; GKO liver-specific Scd3 ; HC ; high sucrose ; high-carbohydrate ; WT ; wild-type ; TLC ; thin layer chromatography ; GLC ; gas liquid chromatography ; ALT ; alanine aminotransferase
• 刊名：Journal of Hepatology
• 出版年：2016
• 出版时间：July 2016
• 年：2016
• 卷：65
• 期：1
• 页码：103-112
• 全文大小：1785 K

文摘

High-carbohydrate diets contribute to the development of liver stress and fatty liver disease. While saturated fatty acids are known to induce liver stress, the role of monounsaturated fatty acids (MUFA), synthesized by the stearoyl-CoA desaturase (SCD) family of enzymes, in regulation of liver function during lipogenic dietary conditions remains largely unknown. The major products of SCD-catalyzed reactions are oleate (18:1n-9) and palmitoleate (16:1n-7).

Methods

We generated mouse models with restricted exogenous MUFA supply and reduced endogenous MUFA synthesis, in which SCD1 global knockout (GKO) or liver-specific knockout (LKO) mice were fed a lipogenic high-sucrose very low-fat (HSVLF) or high-carbohydrate (HC) diet. In a gain-of-function context, we introduced liver-specific expression of either human SCD5, which synthesizes 18:1n-9, or mouse Scd3, which synthesizes 16:1n-7, into SCD1 GKO mice and fed the HSVLF diet.

Results

Lipogenic high-carbohydrate diets induced hepatic endoplasmic reticulum (ER) stress and inflammation in SCD1 GKO and LKO mice. Dietary supplementation with 18:1n-9, but not 18:0, prevented the HSVLF diet-induced hepatic ER stress and inflammation in SCD1 LKO mice, while hepatic SCD5, but not Scd3, expression reduced the ER stress and inflammation in GKO mice. Additional experiments revealed liver-specific deletion of the transcriptional coactivator PGC-1α reduced hepatic inflammatory and ER stress response gene expression in SCD1 LKO mice.

Conclusions

Our results demonstrate an indispensable role of hepatic oleate in protection against lipogenic diet-induced hepatic injury, and PGC-1α potentiates the ER stress response under conditions of restricted dietary oleate coupled to reduced capacity of endogenous hepatic oleate synthesis.

Lay summary

Susceptibility to metabolic dysfunction is influenced by genetic and environmental factors. In this study we show that modulation of two genes regulates the liver response, including ER stress and inflammation, to a high-carbohydrate low-fat diet. We reveal that hepatic availability of oleate, a monounsaturated fatty acid, is important for maintenance of liver health.