Cholesterol-induced hepatic inflammation does not contribute to the development of insulin resistance in male LDL receptor knockout mice

Anouk Funke, Marijke Schreurs, Marcela Aparicio Vergara, Fareeba Sheedfar, Nanda Gruben, Niels J. Kloosterhuis, Ronit Shiri-Sverdlov, Albert K. Groen, Bart van de Sluis, Marten H. Hofker, Debby P. Y. Koonen*

*Corresponding author voor dit werk

OnderzoeksoutputAcademicpeer review

19 Citaten (Scopus)
141 Downloads (Pure)

Samenvatting

Objective: It is generally assumed that hepatic inflammation in obesity is linked to the pathogenesis of insulin resistance. Several recent studies have shed doubt on this view, which questions the causality of this association. This study focuses on Kupffer cell-mediated hepatic inflammation as a possible driver of insulin resistance in the absence and presence of obesity.

Methods: We used male mice deficient for the low-density lipoprotein receptor (Ldlr(-/-)) and susceptible to cholesterol-induced hepatic inflammation. Whole body and hepatic insulin resistance was measured in mice fed 4 diets for 2 and 15 weeks, i.e., chow, high-fat (HF), HF-cholesterol (HFC; 0.2% cholesterol) and HF without cholesterol (HFnC). Biochemical parameters in plasma and liver were measured and inflammation was determined using immunohistochemistry and RT-PCR.

Results: At 2 weeks, we did not find significant metabolic effects in either diet group, except for the mice fed a HFC diet which showed pronounced hepatic inflammation (p <0.05) but normal insulin sensitivity. At 15 weeks, a significant increase in insulin levels, HOMA-IR, and hepatic insulin resistance was observed in mice fed a HFC, HFnC, and HF diet compared to chow-fed mice (p <0.05). Regardless of the level of hepatic inflammation (HFC > HF, HFnC; p <0.05) insulin resistance in mice fed HFC was no worse compared to mice on a HFnC and HF diet.

Conclusion: These data show that cholesterol-induced hepatic inflammation does not contribute to the development of insulin resistance in male Ldlr(-/-) mice. This study suggests that Kupffer cell-driven hepatic inflammation is a consequence, not a cause, of metabolic dysfunction in obesity. (C) 2013 Elsevier Ireland Ltd. All rights reserved.

Originele taal-2English
Pagina's (van-tot)390-396
Aantal pagina's7
TijdschriftAtherosclerosis
Volume232
Nummer van het tijdschrift2
DOI's
StatusPublished - feb.-2014

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