School of Medical Sciences, UNSW Sydney, Sydney, New South Wales, Australia.
Garvan Institute of Medical Research, St Vincent's Clinical School, UNSW Sydney, Sydney, New South Wales, Australia.
Am J Physiol Endocrinol Metab. 2021 Jul 1;321(1):E176-E189. doi: 10.1152/ajpendo.00446.2020. Epub 2021 Jun 14.
Almost 40% of adults worldwide are classified as overweight or obese. Exercise is a beneficial intervention in obesity, partly due to increases in mitochondrial activity and subsequent increases in nicotinamide adenine dinucleotide (NAD), an important metabolic cofactor. Recent studies have shown that increasing NAD levels through pharmacological supplementation with precursors such as nicotinamide mononucleotide (NMN) improved metabolic health in high-fat-diet (HFD)-fed mice. However, the effects of combined exercise and NMN supplementation are unknown. Thus, here we examined the combined effects of NMN and treadmill exercise in female mice with established obesity after 10 wk of diet. Five-week-old female C57BL/6J mice were exposed to a control diet ( = 16) or HFD. Mice fed a HFD were either untreated (HFD; = 16), received NMN in drinking water (400 mg/kg; HNMN; = 16), were exposed to treadmill exercise 6 days/wk (HEx; = 16), or were exposed to exercise combined with NMN (HNEx; = 16). Although some metabolic benefits of NMN have been described, at this dose, NMN administration impaired several aspects of exercise-induced benefits in obese mice, including glucose tolerance, glucose-stimulated insulin secretion from islets, and hepatic triglyceride accumulation. HNEx mice also exhibited increased antioxidant and reduced prooxidant gene expression in both islets and muscle, suggesting that altered redox status is associated with the loss of exercise-induced health benefits with NMN cotreatment. Our data show that NMN treatment impedes the beneficial metabolic effects of exercise in a mouse model of diet-induced obesity in association with disturbances in redox metabolism. NMN dampened exercise-induced benefits on glucose handling in diet-induced obesity. NMN administration alongside treadmill exercise enhanced the ratio of antioxidants to prooxidants. We suggest that NMN administration may not be beneficial when NAD levels are replete.
全球近 40%的成年人被归类为超重或肥胖。运动是肥胖的有益干预措施,部分原因是线粒体活性增加,随后烟酰胺腺嘌呤二核苷酸(NAD)增加,NAD 是一种重要的代谢辅助因子。最近的研究表明,通过药理学补充烟酰胺单核苷酸(NMN)等前体来增加 NAD 水平,可以改善高脂肪饮食(HFD)喂养的小鼠的代谢健康。然而,联合运动和 NMN 补充的效果尚不清楚。因此,在这里,我们在饮食 10 周后检查了 NMN 和跑步机运动对肥胖雌性小鼠的联合影响。将 5 周龄的雌性 C57BL/6J 小鼠暴露于对照饮食( = 16)或 HFD。喂食 HFD 的小鼠未处理(HFD; = 16),或在饮用水中给予 NMN(400mg/kg;HNMN; = 16),每周 6 天暴露于跑步机运动(HEx; = 16),或暴露于运动与 NMN 联合(HNEx; = 16)。尽管已经描述了 NMN 的一些代谢益处,但在此剂量下,NMN 给药会损害肥胖小鼠中运动诱导益处的几个方面,包括葡萄糖耐量、胰岛葡萄糖刺激的胰岛素分泌和肝甘油三酯积累。HNEx 小鼠的胰岛和肌肉中的抗氧化和减少的促氧化剂基因表达也增加,这表明氧化还原状态的改变与 NMN 伴随治疗时运动诱导的健康益处丧失有关。我们的数据表明,NMN 治疗会干扰饮食诱导肥胖小鼠模型中运动的有益代谢作用,同时还会干扰氧化还原代谢。NMN 减弱了运动对饮食诱导肥胖中葡萄糖处理的有益作用。NMN 给药与跑步机运动相结合增强了抗氧化剂与促氧化剂的比例。我们建议,当 NAD 水平充足时,NMN 给药可能不会有益。