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Allomyrina dichotoma larva extract attenuates free fatty acid-induced lipotoxicity in pancreatic beta cells.
Kim, Kyong; Kwak, Min-Kyu; Bae, Gong-Deuk; Park, Eun-Young; Baek, Dong-Jae; Kim, Chul-Young; Jang, Se-Eun; Jun, Hee-Sook; Oh, Yoon Sin.
Affiliation
  • Kim K; Department of Food Nutrition, College of Bio Convergence, Eulji University, Seongnam 13135, Korea.
  • Kwak MK; Department of Food Nutrition, College of Bio Convergence, Eulji University, Seongnam 13135, Korea.
  • Bae GD; Institute of Lee Gil Ya Cancer and Diabetes, Department of Molecular Medicine, Gachon University, Incheon 21999, Korea.
  • Park EY; College of Pharmacy and Natural Medicine Research Institute, Mokpo National University, Muan 58554, Korea.
  • Baek DJ; College of Pharmacy and Natural Medicine Research Institute, Mokpo National University, Muan 58554, Korea.
  • Kim CY; College of Pharmacy, Hanyang University, Ansan 15588, Korea.
  • Jang SE; Department of Food Nutrition, College of Bio Convergence, Eulji University, Seongnam 13135, Korea.
  • Jun HS; College of Pharmacy and Gachon Institute of Pharmaceutical Science, Gachon University, Incheon 21936, Korea.
  • Oh YS; Department of Food Nutrition, College of Bio Convergence, Eulji University, Seongnam 13135, Korea.
Nutr Res Pract ; 15(3): 294-308, 2021 Jun.
Article de En | MEDLINE | ID: mdl-34093971
ABSTRACT
BACKGROUD/

OBJECTIVES:

Allomyrina dichotoma larva (ADL), one of the many edible insects recognized as future food resources, has a range of pharmacological activities. In a previous study, an ADL extract (ADLE) reduced the hepatic insulin resistance of high-fat diet (HFD)-induced diabetic mice. On the other hand, the associated molecular mechanisms underlying pancreatic beta-cell dysfunction remain unclear. This study examined the effects of ADLE on palmitate-induced lipotoxicity in a beta cell line of a rat origin, INS-1 cells. MATERIALS/

METHODS:

ADLE was administered to high-fat diet treated mice. The expression of apoptosis-related molecules was measured by Western blotting, and reactive oxidative stress generation and nitric oxide production were measured by DCH-DA fluorescence and a Griess assay, respectively.

RESULTS:

The administration of ADLE to HFD-induced diabetic mice reduced the hyperplasia, 4-hydroxynonenal levels, and the number of apoptotic cells while improving the insulin levels compared to the HFD group. Treatment of INS-1 cells with palmitate reduced insulin secretion, which was attenuated by the ADLE treatment. Furthermore, the ADLE treatment prevented palmitate-induced cell death in INS-1 cells and isolated islets by reducing the apoptotic signaling molecules, including cleaved caspase-3 and PARP, and the Bax/Bcl2 ratio. ADLE also reduced the levels of reactive oxygen species generation, lipid accumulation, and nitrite production in palmitate-treated INS-1 cells while increasing the ATP levels. This effect corresponded to the decreased expression of inducible nitric oxide synthase (iNOS) mRNA and protein.

CONCLUSIONS:

ADLE helps prevent lipotoxic beta-cell death in INS-1 cells and HFD-diabetic mice, suggesting that ADLE can be used to prevent or treat beta-cell damage in glucose intolerance during the development of diabetes.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Nutr Res Pract Année: 2021 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Nutr Res Pract Année: 2021 Type de document: Article