Transgenic n-3 PUFAs enrichment leads to weight loss via modulating neuropeptides in hypothalamus

Neurosci Lett. 2016 Jan 12:611:28-32. doi: 10.1016/j.neulet.2015.11.029. Epub 2015 Dec 2.

Abstract

Body weight is related to fat mass, which is associated with obesity. Our study explored the effect of fat-1 gene on body weight in fat-1 transgenic mice. In present study, we observed that the weight/length ratio of fat-1 transgenic mice was lower than that of wild-type mice. The serum levels of triglycerides (TG), cholesterol (CT), high-density lipoprotein cholesterol (HDL-c), low-density lipoprotein cholesterol (LDL-c) and blood glucose (BG) in fat-1 transgenic mice were all decreased. The weights of peri-bowels fat, perirenal fat and peri-testicular fat in fat-1 transgenic mice were reduced. We hypothesized that increase of n-3 PUFAs might alter the expression of hypothalamic neuropeptide genes and lead to loss of body weight in fat-1 transgenic mice. Therefore, we measured mRNA levels of appetite neuropeptides, Neuropeptide Y (NPY), Agouti-related peptides (AgRP), Proopiomelanocortin (POMC), Cocaine and amphetamine regulated transcript (CART), ghrelin and nesfatin-1 in hypothalamus by real-time PCR. Compared with wild-type mice, the mRNA levels of CART, POMC and ghrelin were higher, while the mRNA levels of NPY, AgRP and nesfatin-1 were lower in fat-1 transgenic mice. The results indicate that fat-1 gene or n-3 PUFAs participates in regulation of body weight, and the mechanism of this phenomenon involves the expression of appetite neuropeptides and lipoproteins in fat-1 transgenic mice.

Keywords: Body weight; Fat-1 gene; Hypothalamus; Neuropeptide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / anatomy & histology
  • Animals
  • Appetite / genetics
  • Blood Glucose / metabolism
  • Body Size / genetics
  • Cadherins / genetics*
  • Cholesterol / blood
  • Fatty Acids, Omega-3 / metabolism*
  • Hypothalamus / metabolism*
  • Male
  • Mice, Transgenic
  • Neuropeptides / genetics
  • Neuropeptides / metabolism*
  • RNA, Messenger / metabolism
  • Triglycerides / blood
  • Weight Loss / genetics*

Substances

  • Blood Glucose
  • Cadherins
  • Fatty Acids, Omega-3
  • Neuropeptides
  • RNA, Messenger
  • Triglycerides
  • fat1 protein, mouse
  • Cholesterol