Center for Human Nutrition, Washington University School of Medicine, St Louis, Missouri, USA.
Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Endocrinology. 2021 Mar 1;162(3). doi: 10.1210/endocr/bqab006.
Nicotinamide adenine dinucleotide (NAD+) is an essential coenzyme that regulates cellular energy metabolism in many cell types. The major purpose of the present study was to test the hypothesis that NAD+ in white adipose tissue (WAT) is a regulator of whole-body metabolic flexibility in response to changes in insulin sensitivity and with respect to substrate availability and use during feeding and fasting conditions. To this end, we first evaluated the relationship between WAT NAD+ concentration and metabolic flexibility in mice and humans. We found that WAT NAD+ concentration was increased in mice after calorie restriction and exercise, 2 enhancers of metabolic flexibility. Bariatric surgery-induced 20% weight loss increased plasma adiponectin concentration, skeletal muscle insulin sensitivity, and WAT NAD+ concentration in people with obesity. We next analyzed adipocyte-specific nicotinamide phosphoribosyltransferase (Nampt) knockout (ANKO) mice, which have markedly decreased NAD+ concentrations in WAT. ANKO mice oxidized more glucose during the light period and after fasting than control mice. In contrast, the normal postprandial stimulation of glucose oxidation and suppression of fat oxidation were impaired in ANKO mice. Data obtained from RNA-sequencing of WAT suggest that loss of NAMPT increases inflammation, and impairs insulin sensitivity, glucose oxidation, lipolysis, branched-chain amino acid catabolism, and mitochondrial function in WAT, which are features of metabolic inflexibility. These results demonstrate a novel function of WAT NAMPT-mediated NAD+ biosynthesis in regulating whole-body metabolic flexibility, and provide new insights into the role of adipose tissue NAD+ biology in metabolic health.
烟酰胺腺嘌呤二核苷酸(NAD+)是一种必需的辅酶,可调节许多细胞类型的细胞能量代谢。本研究的主要目的是检验以下假说,即在白色脂肪组织(WAT)中,NAD+是一种调节全身代谢灵活性的物质,可响应胰岛素敏感性的变化以及在进食和禁食条件下的底物可用性和利用情况而变化。为此,我们首先评估了 WAT NAD+浓度与小鼠和人类代谢灵活性之间的关系。我们发现,卡路里限制和运动后,小鼠的 WAT NAD+浓度增加,这是代谢灵活性的两种增强剂。减肥手术引起的 20%体重减轻增加了肥胖人群的血浆脂联素浓度、骨骼肌胰岛素敏感性和 WAT NAD+浓度。接下来,我们分析了脂肪细胞特异性烟酰胺磷酸核糖转移酶(Nampt)敲除(ANKO)小鼠,这些小鼠的 WAT NAD+浓度明显降低。ANKO 小鼠在光照期和禁食后比对照小鼠氧化更多的葡萄糖。相比之下,ANKO 小鼠的正常餐后葡萄糖氧化刺激和脂肪氧化抑制受损。WAT 的 RNA 测序数据表明,NAMPT 的缺失会增加炎症,并损害 WAT 中的胰岛素敏感性、葡萄糖氧化、脂肪分解、支链氨基酸分解代谢和线粒体功能,这些都是代谢灵活性受损的特征。这些结果表明 WAT NAMPT 介导的 NAD+生物合成在调节全身代谢灵活性方面具有新的功能,并为脂肪组织 NAD+生物学在代谢健康中的作用提供了新的见解。