A cottonseed oil-enriched diet improves liver and plasma lipid levels in a male mouse model of fatty liver.
Yura SonJay ShockeyMichael K DowdJosephine G ShiehJamie A CooperChad M PatonPublished in: American journal of physiology. Regulatory, integrative and comparative physiology (2022)
A high-fat (HF) diet causes fatty liver, hyperlipidemia, and hypercholesterolemia, and cottonseed oil (CSO) has been shown to improve liver and plasma lipids in human and mouse models. The purpose of this study was to determine the effect of CSO vs. olive oil (OO)-enriched diets on lipid levels in a HF-diet model of fatty liver disease. We placed mice on a HF diet to induce obesity and fatty liver, after which mice were placed on CSO or OO diets, with chow and HF (5.1 kcal/g) groups as control. When CSO- and OO-fed mice were given isocaloric diets with the HF group, there were no differences in body weight, plasma, or hepatic lipids. However, when the CSO and OO diets were reduced in calories (4.0 kcal/g), CSO and OO groups reduced body weight. The CSO group had lower plasma total cholesterol (-56 ± 6%, P < 0.01), free cholesterol (-53 ± 7%, P < 0.01), triglycerides (-61 ± 14%, P < 0.01), and LDL (-42 ± 16%, P = 0.01) vs. HF group whereas the OO diet lowered LDL (-18 ± 12%, P = 0.05) vs. HF. Furthermore, the CSO diet decreased hepatic total cholesterol (-40 ± 12%, P < 0.01), free cholesterol (-23 ± 11%, P = 0.04), and triglycerides (-47 ± 12%, P = 0.02). There were no significant changes in lipogenesis and fatty acid oxidation among the groups. However, the CSO group increased lipid oxidative gene expression in liver and dihydrosterculic acid increased PPARα target genes with in vitro models. Taken together, consuming a reduced calorie diet enriched in CSO reduces liver and plasma lipid profiles in an obese model of fatty liver.
Keyphrases
- weight loss
- fatty acid
- bariatric surgery
- body weight
- physical activity
- mouse model
- gene expression
- high fat diet induced
- low density lipoprotein
- acute heart failure
- metabolic syndrome
- type diabetes
- insulin resistance
- adipose tissue
- coronary artery disease
- endothelial cells
- skeletal muscle
- dna methylation
- transcription factor
- cardiovascular events
- hydrogen peroxide
- genome wide identification