Journal
FOOD SCIENCE AND HUMAN WELLNESS
Volume 11, Issue 4, Pages 1076-1085Publisher
KEAI PUBLISHING LTD
DOI: 10.1016/j.fshw.2022.03.034
Keywords
Metabolic syndrome; Insulin resistance; Insulin signaling pathway; PPAR gamma; Pomegranate peel polyphenols
Categories
Funding
- National Natural Science Foundation of China [31871801, 32001679]
- Science and Technology Research of Shaanxi Province [2020QFY08-03]
- Forestry Science and Technology Programs of Shaanxi Province [SXLK2020-0213]
- Fundamental Research Funds for the Central Universities [GK201604013]
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This study investigated the potential of pomegranate peel polyphenols (PPPs) in preventing the development of metabolic syndrome (MetS) by improving insulin resistance (IR). The results showed that PPPs treatment reversed the negative effects of high fat diet-induced insulin resistance, including disordered glucose and lipid metabolism, and muscle fiber morphology. PPPs treatment increased the protein expressions of insulin receptor (InsR) and phosphorylated insulin receptor substrate 1 (IRS-1), stimulated peroxisome proliferator activated receptor gamma (PPAR gamma) and phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT/PKB) signaling pathway, as well as increased the protein levels of phosphorylated glycogen synthase kinase-3 beta (GSK-3 beta) and glucose transporter 4 (GLUT4). These findings suggest that PPPs have beneficial effects in alleviating insulin resistance by enhancing insulin sensitivity and regulating glucose metabolism.
Insulin resistance (IR) has been considered to be an important causative factor of metabolic syndrome (MetS). The present study investigated whether pomegranate peel polyphenols (PPPs) could prevent the development of MetS by improving IR in rats. Male Sprague-Dawley (SD) rats were fed high fat diet (HFD) to induce MetS and supplemented with different dosages of PPPs for 12 weeks. The results showed that HFD-induced insulin resistant rats had disordered metabolism of blood glucose, blood lipid. and terrible muscle fiber morphology when compared with normal diet-fed rats, but PPPs treatment at a dosage of 300 mg/kg.day significantly reversed these negative effects. Moreover, in skeletal muscle tissue of insulin resistant rats, PPPs treatments significantly increased the protein expressions of insulin receptor (InsR) and phosphorylated insulin receptor substrate 1 (IRS-1), stimulated peroxisome proliferator activated receptor gamma (PPAR gamma) and phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT/PKB) signaling pathway, and aggrandized the protein levels of phosphorylated glycogen synthase kinase-3 beta (GSK-3 beta) and glucose transporter 4 (GLUT4). Our results suggest that PPPs possess of the beneficial effects on alleviating IR by enhancing insulin sensitivity and regulating glucose metabolism. (C) 2022 Beijing Academy of Food Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.
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