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Mill. Fruits Ameliorate Hepatic Glycolipid Metabolism Disorder in Rats Induced by High Fat/High Sugar Diet

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Journal Nutrients
Date 2021 Dec 28
PMID 34960032
Citations 3
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Abstract

Hepatic glycolipid metabolism disorder is considered as one of the key factors in the pathogenesis of many chronic diseases. The objective of this study was to investigate the protective effect and underlying mechanisms of Mill. fruits against hepatic glycolipid metabolic disorders in rats induced by a high fat/high sugar diet. Results showed that ethanol extract, especially at a dose of 600 mg/kg b.w., could effectively ameliorate glycolipid metabolic disorders in rats. The biochemical indexes, including CAT, GSH and HOMA-IR, were significantly improved by the administration of ethanol extract. Immunohistochemistry and Western blot analysis revealed that ethanol extract up-regulated the expression levels of PI3K/AKT, PPAR-α, and the phosphorylation of IRS1 and AMPK proteins, and down-regulated the expressions of SREBP-1 and FAS proteins in the liver, which are closely related to hepatic glycolipid metabolism. Those findings suggested that Mill. fruits could be developed as functional foods and/or nutraceuticals for preventing or controlling some chronic diseases related to hepatic glycolipid metabolism disorder.

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References
1.
Harford K, Reynolds C, McGillicuddy F, Roche H . Fats, inflammation and insulin resistance: insights to the role of macrophage and T-cell accumulation in adipose tissue. Proc Nutr Soc. 2011; 70(4):408-17. DOI: 10.1017/S0029665111000565. View

2.
Perry R, Samuel V, Petersen K, Shulman G . The role of hepatic lipids in hepatic insulin resistance and type 2 diabetes. Nature. 2014; 510(7503):84-91. PMC: 4489847. DOI: 10.1038/nature13478. View

3.
Laleh P, Yaser K, Abolfazl B, Shahriar A, Mohammad A, Nazila F . Oleoylethanolamide increases the expression of PPAR-Α and reduces appetite and body weight in obese people: A clinical trial. Appetite. 2018; 128:44-49. DOI: 10.1016/j.appet.2018.05.129. View

4.
Chen C, Han X, Dong P, Li Z, Yanagita T, Xue C . Sea cucumber saponin liposomes ameliorate obesity-induced inflammation and insulin resistance in high-fat-diet-fed mice. Food Funct. 2018; 9(2):861-870. DOI: 10.1039/c7fo01599b. View

5.
Nagle C, Klett E, Coleman R . Hepatic triacylglycerol accumulation and insulin resistance. J Lipid Res. 2008; 50 Suppl:S74-9. PMC: 2674743. DOI: 10.1194/jlr.R800053-JLR200. View