Enhancing natriuretic peptide signaling in adipose tissue, but not in muscle, protects against diet-induced obesity and insulin resistance

• Published in: Science signaling 2017-07, Vol.10 (489)
• Main Authors: Wu, Wei, Shi, Fubiao, Liu, Dianxin, Ceddia, Ryan P, Gaffin, Robert, Wei, Wan, Fang, Huafeng, Lewandowski, E Douglas, Collins, Sheila
• Format: Article
• Language: English
• Subjects: Adipose Tissue - metabolism; Adipose Tissue - pathology; Animals; Dietary Fats - adverse effects; Dietary Fats - pharmacology; Insulin Resistance; Mice; Mice, Knockout; Obesity - chemically induced; Obesity - genetics; Obesity - metabolism; Receptors, Atrial Natriuretic Factor - genetics; Receptors, Atrial Natriuretic Factor - metabolism; Signal Transduction - drug effects; Signal Transduction - genetics
• ISSN: 1945-0877; 1937-9145
• 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.