scholarly journals The Relation Between Fibroblast Growth Factor 21 and Insulin Resistance in hyperlipidemia Patients

2021 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
Rana F. Jasim ◽  
Safaa S. Mohammad ◽  
Thikra A. Allwsh
2020 ◽  
Vol 21 (18) ◽  
pp. 6836
Author(s):  
Hyo Jin Maeng ◽  
Gha Young Lee ◽  
Jae Hyun Bae ◽  
Soo Lim

Fibroblast growth factor 21 (FGF21) is a hormonal regulator of lipid and glucose metabolism. We aimed to investigate the effect of an FGF21 analogue (LY2405319) on the development of atherosclerosis and its associated parameters. ApoE−/− mice were fed an atherogenic diet for 14 weeks and were randomly assigned to control (saline) or FGF21 (0.1 mg/kg) treatment group (n = 10/group) for 5 weeks. Plaque size in the aortic arch/valve areas and cardiovascular risk markers were evaluated in blood and tissues. The effects of FGF21 on various atherogenesis-related pathways were also assessed. Atherosclerotic plaque areas in the aortic arch/valve were significantly smaller in the FGF21 group than in controls after treatment. FGF21 significantly decreased body weight and glucose concentrations, and increased circulating adiponectin levels. FGF21 treatment alleviated insulin resistance and decreased circulating concentrations of triglycerides, which were significantly correlated with plaque size. FGF21 treatment reduced lipid droplets in the liver and decreased fat cell size and inflammatory cell infiltration in the abdominal visceral fat compared with the control group. The monocyte chemoattractant protein-1 levels were decreased and β-hydroxybutyrate levels were increased by FGF21 treatment. Uncoupling protein 1 expression in subcutaneous fat was greater and fat cell size in brown fat was smaller in the FGF21 group compared with controls. Administration of FGF21 showed anti-atherosclerotic effects in atherosclerosis-prone mice and exerted beneficial effects on critical atherosclerosis pathways. Improvements in inflammation and insulin resistance seem to be mechanisms involved in the mitigation of atherosclerosis by FGF21 therapy.


PLoS ONE ◽  
2013 ◽  
Vol 8 (3) ◽  
pp. e55632 ◽  
Author(s):  
Birgitte Lindegaard ◽  
Thine Hvid ◽  
Thomas Grøndahl ◽  
Christian Frosig ◽  
Jan Gerstoft ◽  
...  

Metabolism ◽  
2010 ◽  
Vol 59 (1) ◽  
pp. 33-37 ◽  
Author(s):  
Sebastian Stein ◽  
Holger Stepan ◽  
Jürgen Kratzsch ◽  
Michael Verlohren ◽  
Hans-Joachim Verlohren ◽  
...  

2015 ◽  
Vol 47 ◽  
pp. 236
Author(s):  
Arun Maharaj ◽  
Aaron L. Slusher ◽  
Michael Whitehurst ◽  
Robert F. Zoeller ◽  
James T. Mock ◽  
...  

2021 ◽  
pp. 1-14
Author(s):  
Haizhao Song ◽  
Xinchun Shen ◽  
Qiang Chu ◽  
Xiaodong Zheng

BACKGROUND: Red raspberry (Rubus idaeus L.), a natural dietary source of (poly)phenols, has been used as medicine for centuries. OBJECTIVE: The purpose of this study is to determine the effect of a red raspberry (poly)phenolic extract (RPE) on diet-induced obesity, hepatic steatosis and insulin resistance, and elucidate the underlying molecular mechanisms. METHODS: Male specific pathogen-free C57BL/6J mice were randomly divided into three groups (n = 12 per group), and fed with low-fat diet (10% fat energy), high-fat diet (HFD, 45% fat energy), or HFD supplemented with RPE of 150 mg/kg body weight by intragastric administration for 14 weeks. Obesity-related biochemical indexes and hepatic gene expression levels were determined. The statistical analyses were conducted using one-way analysis of variance (ANOVA) followed by Duncan’s multiple range test. RESULTS: The body weight gain, steatosis grade scores and insulin resistance index in the RPE group decreased by 34.48% (P = 0.00), 58.82% (P = 0.00), and 53.77% (P = 0.00), respectively, compared to those in the HFD group. Moreover, RPE supplement significantly changed the expression profile of the genes involved in lipid metabolism and fibroblast growth factor 21 signaling pathway. CONCLUSIONS: This study demonstrated that RPE protected from diet-induced obesity and related metabolic disorders by improving the lipid metabolism and fibroblast growth factor 21 resistance.


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