Aspalathin-Enriched Green Rooibos Extract Reduces Hepatic Insulin Resistance by Modulating PI3K/AKT and AMPK Pathways

被引:56
|
作者
Mazibuko-Mbeje, Sithandiwe E. [1 ,2 ]
Dludla, Phiwayinkosi V. [1 ]
Roux, Candice [1 ]
Johnson, Rabia [1 ,2 ]
Ghoor, Samira [1 ]
Joubert, Elizabeth [3 ,4 ]
Louw, Johan [1 ,5 ]
Opoku, Andy R. [5 ]
Muller, Christo J. F. [1 ,2 ,5 ]
机构
[1] South African Med Res Council, Biomed Res & Innovat Platform, POB 19070, ZA-7505 Tygerberg, South Africa
[2] Stellenbosch Univ, Div Med Physiol, Fac Hlth Sci, Private Bag X1, ZA-7505 Tygerberg, South Africa
[3] ARC, Plant Bioact Grp Postharvest & Agroproc Technol, Private Bag X5026, ZA-7599 Stellenbosch, South Africa
[4] Stellenbosch Univ, Dept Food Sci, Private Bag X1, ZA-7602 Matieland, South Africa
[5] Univ Zululand, Dept Biochem & Microbiol, Private Bag X1001, ZA-3886 Kwa Dlangezwa, South Africa
来源
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
metabolic syndrome; obesity; insulin resistance; diabetes mellitus; green rooibos extract; therapeutic target; AMPK; PI3K; AKT; ACTIVATED PROTEIN-KINASE; FATTY-ACID OXIDATION; LINEARIS EXTRACT; GLUCOSE-INTOLERANCE; LIPID HOMEOSTASIS; IMPROVES GLUCOSE; LIVER-DISEASE; HERBAL TEA; IRS-1/PI3K/AKT; CARDIOMYOCYTES;
D O I
10.3390/ijms20030633
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We previously demonstrated that an aspalathin-enriched green rooibos extract (GRE) reversed palmitate-induced insulin resistance in C2C12 skeletal muscle and 3T3-L1 fat cells by modulating key effectors of insulin signalling such as phosphatidylinositol-4,5-bisphosphate 3-kinase/protein kinase B (PI3K/AKT) and AMP-activated protein kinase (AMPK). However, the effect of GRE on hepatic insulin resistance is unknown. The effects of GRE on lipid-induced hepatic insulin resistance using palmitate-exposed C3A liver cells and obese insulin resistant (OBIR) rats were explored. GRE attenuated the palmitate-induced impairment of glucose and lipid metabolism in treated C3A cells and improved insulin sensitivity in OBIR rats. Mechanistically, GRE treatment significantly increased PI3K/AKT and AMPK phosphorylation while concurrently enhancing glucose transporter 2 expression. These findings were further supported by marked stimulation of genes involved in glucose metabolism, such as insulin receptor (Insr) and insulin receptor substrate 1 and 2 (Irs1 and Irs2), as well as those involved in lipid metabolism, including Forkhead box protein O1 (FOXO1) and carnitine palmitoyl transferase 1 (CPT1) following GRE treatment. GRE showed a strong potential to ameliorate hepatic insulin resistance by improving insulin sensitivity through the regulation of PI3K/AKT, FOXO1 and AMPK-mediated pathways.
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页数:16
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