Does long-term androgen deficiency lead to metabolic syndrome in middle-aged rats?

Veronika Borbélyová1, Emese Domonkos1, Janka Bábíčková1

  • 1Institute of Molecular Biomedicine, Faculty of Medicine, Comenius University, Sasinkova 4, 811 08 Bratislava, Slovakia.

Experimental Gerontology
|August 16, 2017
PubMed

Insights

Long-term hypogonadism starting before puberty did not cause metabolic syndrome in middle-aged male rats, but may impact liver function. Sex differences in metabolic health are not testosterone-dependent.

Area of Science:

  • Endocrinology
  • Metabolic Syndrome Research
  • Animal Models in Physiology

Background:

  • Hypogonadism is linked to metabolic syndrome in observational and animal studies.
  • Previous research often examines short-term effects of adult-onset androgen deficiency.
  • The impact of prepubertal, long-term hypogonadism on metabolic health remains less understood.

Purpose of the Study:

  • To investigate the long-term metabolic effects of androgen deficiency initiated before puberty.
  • To assess components of the metabolic syndrome in middle-aged male rats with early-onset hypogonadism.

Main Methods:

  • Examined metabolic parameters in adult male rats, female rats, and gonadectomized male rats at 18 months of age.
  • Assessed plasma levels of testosterone, cholesterol, lipoproteins, glucose, insulin, and uric acid.
  • Evaluated liver enzymes, liver triacylglycerol, blood pressure, and oral glucose tolerance tests.

Main Results:

  • Observed sex differences in body weight, glycemia dynamics, plasma testosterone, cholesterol, and HDL.
  • Long-term hypogonadism did not significantly alter blood pressure, glycemia, plasma insulin, or uric acid.
  • Gonadectomized males showed elevated plasma liver enzymes and liver triacylglycerol.

Conclusions:

  • Long-term hypogonadism initiated before puberty does not induce the metabolic syndrome in middle-aged male rats.
  • Early-onset hypogonadism may specifically affect liver parameters.
  • Observed sex differences in metabolic parameters are not mediated by testosterone levels.