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Dark nights reverse metabolic disruption caused by dim light at night

机译:漆黑的夜晚逆转了夜晚昏暗的光线引起的新陈代谢破坏

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Objective The increasing prevalence of obesity and related metabolic disorders coincides with increasing exposure to light at night. Previous studies report that mice exposed to dim light at night (dLAN) develop symptoms of metabolic syndrome. This study investigated whether mice returned to dark nights after dLAN exposure recover metabolic function. Design and Methods Male Swiss-Webster mice were assigned to either: standard light-dark (LD) conditions for 8 weeks (LD/LD), dLAN for 8 weeks (dLAN/dLAN), LD for 4 weeks followed by 4 weeks of dLAN (LD/dLAN), and dLAN for 4 weeks followed by 4 weeks of LD (dLAN/LD). Results After 4 weeks in their respective lighting conditions both groups initially placed in dLAN increased body mass gain compared to LD mice. Half of the dLAN mice (dLAN/LD) were then transferred to LD and vice versa (LD/dLAN). Following the transfer dLAN/dLAN and LD/dLAN mice gained more weight than LD/LD and dLAN/LD mice. At the conclusion of the study dLAN/LD mice did not differ from LD/LD mice with respect to weight gain and had lower fat pad mass compared to dLAN/dLAN mice. Compared to all other groups dLAN/dLAN mice decreased glucose tolerance as indicated by an intraperitoneal glucose tolerance test at week 7, indicating that dLAN/LD mice recovered glucose metabolism. dLAN/dLAN mice also increased MAC1 mRNA expression in peripheral fat as compared to both LD/LD and dLAN/LD mice, suggesting peripheral inflammation is induced by dLAN, but not sustained after return to LD. Conclusion These results suggest that re-exposure to dark nights ameliorates metabolic disruption caused by dLAN exposure.
机译:目的肥胖症和相关代谢紊乱的患病率增加与夜间光照增加有关。先前的研究报告称,夜间暴露于暗光(dLAN)的小鼠会出现代谢综合征的症状。这项研究调查了小鼠是否在dLAN暴露后恢复了黑夜恢复了代谢功能。设计和方法将雄性Swiss-Webster小鼠分配至以下任一条件:标准明暗(LD)条件8周(LD / LD),dLAN 8周(dLAN / dLAN),LD 4周,随后4周dLAN (LD / dLAN),先进行dLAN 4周,再进行LD(dLAN / LD)4周。结果在各自的光照条件下4周后,与LD小鼠相比,两组最初放置在dLAN中的体重增加。然后将一半的dLAN小鼠(dLAN / LD)转移到LD,反之亦然(LD / dLAN)。转移后,dLAN / dLAN和LD / dLAN小鼠比LD / LD和dLAN / LD小鼠体重增加。在研究结束时,与dLAN / dLAN小鼠相比,dLAN / LD小鼠的体重增加与LD / LD小鼠没有区别,并且脂肪垫的质量更低。与所有其他组相比,第7周的腹膜内葡萄糖耐量测试表明dLAN / dLAN小鼠的葡萄糖耐量降低,表明dLAN / LD小鼠恢复了葡萄糖代谢。与LD / LD和dLAN / LD小鼠相比,dLAN / dLAN小鼠还增加了外周脂肪中MAC1 mRNA的表达,这表明dLAN诱导了外周炎症,但回到LD后并没有持续。结论这些结果表明,再次暴露于漆黑的夜晚可改善dLAN暴露引起的代谢破坏。

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