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Obese mothers supplemented with melatonin during gestation and lactation ameliorate the male offspring's pancreatic islet cellular composition and beta-cell function

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CAMBRIDGE UNIV PRESS
DOI: 10.1017/S2040174423000168

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Pancreatic islet; DOHaD; Maternal obesity; Beta-cell; Molecular biology

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Supplementing obese mothers with melatonin during gestation and lactation has benefits for the pancreatic islet cellular composition and beta-cell function in adult male offspring. The study found that melatonin supplementation improved glucose metabolism and weight loss in both mothers and offspring, while reducing pro-inflammatory markers and endoplasmic reticulum stress. Additionally, antioxidant enzymes were improved, beta-cell mass and hyperinsulinemia were reduced, and beta-cell maturity and identity gene expressions were enhanced in the offspring. Overall, melatonin supplementation in obese mothers helps preserve pancreatic islets and functioning beta cells in their offspring.
Melatonin supplementation to obese mothers during gestation and lactation might benefit the pancreatic islet cellular composition and beta-cell function in male offspring adulthood. C57BL/6 females (mothers) were assigned to two groups (n = 20/each) based on their consumption in control (C 17% kJ as fat) or high-fat diet (HF 49% kJ as fat). Mothers were supplemented with melatonin (Mel) (10 mg/kg daily) during gestation and lactation, or vehicle, forming the groups (n = 10/each): C, CMel, HF, and HFMel. The male offspring were studied, considering they only received the C diet after weaning until three months old. The HF mothers and their offspring showed higher body weight, glucose intolerance, insulin resistance, and low insulin sensitivity than the C ones. However, HFMel mothers and their offspring showed improved glucose metabolism and weight loss than the HF ones. Also, the offspring's higher expressions of pro-inflammatory markers and endoplasmic reticulum (ER) stress were observed in HF but reduced in HFMel. Contrarily, antioxidant enzymes were less expressed in HF but improved in HFMel. In addition, HF showed increased beta-cell mass and hyperinsulinemia but diminished in HFMel. Besides, the beta-cell maturity and identity gene expressions diminished in HF but enhanced in HFMel. In conclusion, obese mothers supplemented with melatonin benefit their offspring's islet cell remodeling and function. In addition, improving pro-inflammatory markers, oxidative stress, and ER stress resulted in better glucose and insulin levels control. Consequently, pancreatic islets and functioning beta cells were preserved in the offspring of obese mothers supplemented with melatonin.

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