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http://dx.doi.org/10.4162/nrp.2021.15.3.294

Allomyrina dichotoma larva extract attenuates free fatty acid-induced lipotoxicity in pancreatic beta cells  

Kim, Kyong (Department of Food Nutrition, College of Bio Convergence, Eulji University)
Kwak, Min-Kyu (Department of Food Nutrition, College of Bio Convergence, Eulji University)
Bae, Gong-Deuk (Institute of Lee Gil Ya Cancer and Diabetes, Department of Molecular Medicine, Gachon University)
Park, Eun-Young (College of Pharmacy and Natural Medicine Research Institute, Mokpo National University)
Baek, Dong-Jae (College of Pharmacy and Natural Medicine Research Institute, Mokpo National University)
Kim, Chul-Young (College of Pharmacy, Hanyang University)
Jang, Se-Eun (Department of Food Nutrition, College of Bio Convergence, Eulji University)
Jun, Hee-Sook (College of Pharmacy and Gachon Institute of Pharmaceutical Science, Gachon University)
Oh, Yoon Sin (Department of Food Nutrition, College of Bio Convergence, Eulji University)
Publication Information
Nutrition Research and Practice / v.15, no.3, 2021 , pp. 294-308 More about this Journal
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.
Keywords
Diabetes mellitus; apoptosis; insulin-secreting cells; nitric oxide; oxidative stress;
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