3 / 5
Notes:
conference
series LLC Ltd
Volume 8
Page 20
Oct 25-26, 2018 Budapest, Hungary
21
st
World Obesity Conference
World Obesity-2018
Journal of Obesity & Weight Loss Therapy | ISSN : 2165-7904
Nadezhda Bazhan et al., J Obes Weight Loss Ther 2018, Volume:8
DOI: 10.4172/2165-7904-C10-083
Sex differences in the effect of high-fat diet on mouse white adipose
tissue
Fibroblast growth factor-21 (FGF21) is a circulating hepatokine, favors white adipose
tissue (WAT) glucose utilization and lipolysis in mice. Diet induced obesity (DIO) is
potentially FGF21-resistant state: Increased circulating FGF21 levels are associated
with decreased FGF21 signaling in obese mice. It is unknown whether DIO changes
WAT FGF21 signaling and metabolic gene expressions in a sex-specific manner.
Obesity was induced by high-calorie diet (10 weeks) in C57Bl mice of both sexes.
Blood parameters and visceral WAT expressions of genes involved in FGF21 signaling
(FGF21, PPARγ, PGC1α, KLB), glucose input (SLC2A1, SLC2A4), lipolysis (Hsl),
lipogenesis (Lpl), fatty acid oxidation (Cpt1), and thermogenesis (Ucp1) were analyzed
by RT-PCR. DIO increased WAT indexes and circulating FGF21 levels in mice of both
sexes, but WAT content was much higher and FGF21 blood levels were much lower in
obese females than in obese males. DIO induced WAT FGF21 gene expression only
in male. There were signs of FGF21 resistance (reduced Pgc1α and Slc1a expression)
in WAT of obese males. However, increased circulating FGF21 levels and local WAT
FGF21 expression seem to ensure adequate expression of other FGF21 target genes
and reduced WAT accumulation in obese males as compared to females. There were
signs of FGF21 resistance, insulin resistance, and dysregulation of lipid turnover
(reduced PPARΓ, SLC2A4, HSL, and LPL expression) in WAT of obese females. These
transcription changes in combination with low circulating FGF21 level could lead to
pronounce WAT accumulation in obese females.
The study was supported by the Russian Science Foundation, Grant No 17-15-01036.
Biography
Bazhan N is currently a Chief Researcher at the Institute of Cytology and Genetics, Russian Academy of Sciences
and Professor of Novosibirsk State University. She studied on molecular-physiological mechanisms underlying
genetic melanocortin obesity, the role of central melanocortin system in the development of stress-induced anorexia;
the role of hypothalamo-pituitary-adrenal axis in the food-intake regulation and the mechanisms of metabolic
changes associated with age in mice.
bazhan-nm@yandex.ruNadezhda Bazhan
The Institute of Cytology and Genetics,
Russia, Federation
Co-Author
Yakovleva T, Dubinina A
and Makarova E
The Institute of Cytology and Genetics,
Russia, Federation