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Ameliorative Effect of Annona muricata (Graviola) Extract on Hyperglycemia Induced Hepatic Damage in Type 2 Diabetic Mice.
Son, Yiseul; Lee, Heaji; Son, Su-Young; Lee, Choong-Hwan; Kim, Sun-Yeou; Lim, Yunsook.
Afiliación
  • Son Y; Department of Food and Nutrition, Kyung Hee University, 26 Kyung Hee-Daero, Seoul 02447, Korea.
  • Lee H; Department of Food and Nutrition, Kyung Hee University, 26 Kyung Hee-Daero, Seoul 02447, Korea.
  • Son SY; Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, Korea.
  • Lee CH; Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, Korea.
  • Kim SY; Gachon Institute of Pharmaceutical Science, Gachon University, #191, Hambakmoero, Incheon 21936, Korea.
  • Lim Y; Department of Food and Nutrition, Kyung Hee University, 26 Kyung Hee-Daero, Seoul 02447, Korea.
Antioxidants (Basel) ; 10(10)2021 Sep 29.
Article en En | MEDLINE | ID: mdl-34679681
ABSTRACT
Annona muricata (AM) is evergreen plant of the Annonaceae family and known to have anticancer and antidiabetic effects. However, anti-diabetic mechanisms of AM extracts (AME) associated with hepatic glucose regulation and lipid metabolism remain unclear. In this study, we investigated the protective effect of AME extracted on hepatic damage in diabetic mice. Diabetes was induced by a high-fat diet with two-times streptozotocin (STZ) injection (60 mg/kg BW) in C57BL/6 male mice. The diabetic mice were daily administered with AME (50 or 100 mg/kg BW) by gavage for 9 weeks. Biomarkers related to energy metabolism and insulin signaling were examined to identify the effect of AME on hyperglycemia induced hepatic damage. AME supplementation reduced levels of FBG, HbA1c, HOMA-IR and hepatic lipid profiles as well as enhanced insulin signaling by increased the protein levels of IRS-1 accompanied GLUT2 in diabetic mice. Especially low dose of AME showed the beneficial effect of reducing oxidative stress (4-HNE, protein carbonyls, Nrf2, NQO1) and improved hepatic morphology demonstrated by lipid droplets along with upregulation of lipophagy (pAMPK, p-mTOR/mTOR, LC3-2/LC3-1) in diabetic mice. Moreover, AME supplementation ameliorated hepatic lipid metabolism (FAS, SREBP1c, C/EBPα, PPARγ, CPT1A, PPARα) and energy metabolism (pAMPK, PGC1α) in diabetic mice. Taken together, this study suggested that AME could be helpful to prevent hepatic abnormality by regulation of insulin signaling associated with energy metabolism and autophagy in diabetes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Antioxidants (Basel) Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Antioxidants (Basel) Año: 2021 Tipo del documento: Article