Neurosecretory protein GL stimulates food intake, de novo lipogenesis, and onset of obesity.
Eiko Iwakoshi-UkenaKenshiro ShikanoKunihiro KondoShusuke TaniuchiMegumi FurumitsuYuta OchiTsutomu SasakiShiki OkamotoGeorge E BentleyLance J KriegsfeldYasuhiko MinokoshiKazuyoshi UkenaPublished in: eLife (2017)
Mechanisms underlying the central regulation of food intake and fat accumulation are not fully understood. We found that neurosecretory protein GL (NPGL), a newly-identified neuropeptide, increased food intake and white adipose tissue (WAT) in rats. NPGL-precursor gene overexpression in the hypothalamus caused increases in food intake, WAT, body mass, and circulating insulin when fed a high calorie diet. Intracerebroventricular administration of NPGL induced de novo lipogenesis in WAT, increased insulin, and it selectively induced carbohydrate intake. Neutralizing antibody administration decreased the size of lipid droplets in WAT. Npgl mRNA expression was upregulated by fasting and low insulin levels. Additionally, NPGL-producing cells were responsive to insulin. These results point to NPGL as a novel neuronal regulator that drives food intake and fat deposition through de novo lipogenesis and acts to maintain steady-state fat level in concert with insulin. Dysregulation of NPGL may be a root cause of obesity.
Keyphrases
- type diabetes
- adipose tissue
- insulin resistance
- high fat diet induced
- glycemic control
- weight loss
- metabolic syndrome
- fatty acid
- high glucose
- diabetic rats
- weight gain
- induced apoptosis
- transcription factor
- high fat diet
- blood pressure
- protein protein
- blood glucose
- cell cycle arrest
- drug induced
- blood brain barrier
- dna methylation
- cancer therapy
- genome wide
- skeletal muscle
- signaling pathway
- body mass index
- copy number
- cell death
- endothelial cells
- dengue virus
- subarachnoid hemorrhage