Von Willebrand Factor Deficiency Improves Hepatic Steatosis, Insulin Resistance, and Inflammation in Mice Fed High‐Fat Diet

Objective The aim of this study was to investigate the effect of Von Willebrand factor (VWF) on high‐fat diet (HFD)‐induced hepatic steatosis, insulin resistance, and inflammation in mice. Methods The expression of VWF was detected in obese mice. Wild‐type and VWF knockout mice were fed a normal cho...

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Veröffentlicht in:Obesity (Silver Spring, Md.) Md.), 2020-04, Vol.28 (4), p.756-764
Hauptverfasser: Yang, Juan, Lu, Yan, Lou, Xudan, Wang, Jian, Yu, Huilin, Bao, Zhijun, Wang, Haidong
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container_end_page 764
container_issue 4
container_start_page 756
container_title Obesity (Silver Spring, Md.)
container_volume 28
creator Yang, Juan
Lu, Yan
Lou, Xudan
Wang, Jian
Yu, Huilin
Bao, Zhijun
Wang, Haidong
description Objective The aim of this study was to investigate the effect of Von Willebrand factor (VWF) on high‐fat diet (HFD)‐induced hepatic steatosis, insulin resistance, and inflammation in mice. Methods The expression of VWF was detected in obese mice. Wild‐type and VWF knockout mice were fed a normal chow diet or an HFD, and then biomedical, histological, and metabolic analyses were conducted to identify pathologic alterations. Inflammatory cytokine levels and the number of hepatic macrophages were determined in these mice fed an HFD. Results VWF expression was significantly increased in obese mice. VWF−/− mice were less obese and had improved hepatic steatosis, balance of lipid metabolism, and insulin resistance in response to HFD. Furthermore, VWF deficiency attenuated HFD‐induced systemic and hepatic inflammation. In addition, VWF deficiency rescued the abnormal accumulation of hepatic macrophages. Conclusions These data demonstrated VWF deficiency improves hepatic steatosis, insulin resistance, and inflammation. Furthermore, the protective effects are mediated via regulation of hepatic macrophages.
doi_str_mv 10.1002/oby.22744
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Methods The expression of VWF was detected in obese mice. Wild‐type and VWF knockout mice were fed a normal chow diet or an HFD, and then biomedical, histological, and metabolic analyses were conducted to identify pathologic alterations. Inflammatory cytokine levels and the number of hepatic macrophages were determined in these mice fed an HFD. Results VWF expression was significantly increased in obese mice. VWF−/− mice were less obese and had improved hepatic steatosis, balance of lipid metabolism, and insulin resistance in response to HFD. Furthermore, VWF deficiency attenuated HFD‐induced systemic and hepatic inflammation. In addition, VWF deficiency rescued the abnormal accumulation of hepatic macrophages. Conclusions These data demonstrated VWF deficiency improves hepatic steatosis, insulin resistance, and inflammation. Furthermore, the protective effects are mediated via regulation of hepatic macrophages.</description><identifier>ISSN: 1930-7381</identifier><identifier>EISSN: 1930-739X</identifier><identifier>DOI: 10.1002/oby.22744</identifier><identifier>PMID: 32144880</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Cytokines ; Diet ; Fatty acids ; Food ; Gene expression ; Glucose ; Inflammation ; Insulin resistance ; Kinases ; Laboratory animals ; Lipids ; Liver ; Metabolic disorders ; Obesity ; Proteins ; Studies ; Tumor necrosis factor-TNF</subject><ispartof>Obesity (Silver Spring, Md.), 2020-04, Vol.28 (4), p.756-764</ispartof><rights>2020 The Obesity Society</rights><rights>2020 The Obesity Society.</rights><rights>Copyright Blackwell Publishing Ltd. 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source Wiley Online Library Journals Frontfile Complete; Wiley Online Library Free Content
subjects Cytokines
Diet
Fatty acids
Food
Gene expression
Glucose
Inflammation
Insulin resistance
Kinases
Laboratory animals
Lipids
Liver
Metabolic disorders
Obesity
Proteins
Studies
Tumor necrosis factor-TNF
title Von Willebrand Factor Deficiency Improves Hepatic Steatosis, Insulin Resistance, and Inflammation in Mice Fed High‐Fat Diet
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