Wu Wei, Shi Fubiao, Liu Dianxin, Ceddia Ryan P, Gaffin Robert, Wei Wan, Fang Huafeng, Lewandowski E Douglas, Collins Sheila
Integrative Metabolism Program, Sanford Burnham Prebys Medical Discovery Institute at Lake Nona, Orlando, FL 32827, USA.
Division of Endocrinology and Metabolism, Huashan Hospital, Fudan University, Shanghai 200040, China.
Sci Signal. 2017 Jul 25;10(489):eaam6870. doi: 10.1126/scisignal.aam6870.
In addition to controlling blood pressure, cardiac natriuretic peptides (NPs) can stimulate lipolysis in adipocytes and promote the "browning" of white adipose tissue. NPs may also increase the oxidative capacity of skeletal muscle. To unravel the contribution of NP-stimulated metabolism in adipose tissue compared to that in muscle in vivo, we generated mice with tissue-specific deletion of the NP clearance receptor, NPRC, in adipose tissue ( ) or in skeletal muscle ( ). We showed that, similar to null mice, mice, but not mice, were resistant to obesity induced by a high-fat diet. mice exhibited increased energy expenditure, improved insulin sensitivity, and increased glucose uptake into brown fat. These mice were also protected from diet-induced hepatic steatosis and visceral fat inflammation. These findings support the conclusion that NPRC in adipose tissue is a critical regulator of energy metabolism and suggest that inhibiting this receptor may be an important avenue to explore for combating metabolic disease.
除了控制血压外,心脏利钠肽(NPs)还可以刺激脂肪细胞中的脂肪分解,并促进白色脂肪组织的“褐变”。NPs还可能增加骨骼肌的氧化能力。为了阐明与体内肌肉相比,NP刺激的脂肪组织代谢的贡献,我们构建了在脂肪组织( )或骨骼肌( )中组织特异性缺失NP清除受体NPRC的小鼠。我们发现,与 基因敲除小鼠相似, 小鼠而非 小鼠对高脂饮食诱导的肥胖具有抗性。 小鼠表现出能量消耗增加、胰岛素敏感性改善以及棕色脂肪对葡萄糖摄取增加。这些小鼠还能免受饮食诱导的肝脏脂肪变性和内脏脂肪炎症的影响。这些发现支持了脂肪组织中的NPRC是能量代谢关键调节因子的结论,并表明抑制该受体可能是对抗代谢疾病的一个重要探索途径。