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Testosterone effect on experimental diabetes mellitus in encephalomyocarditis (EMC) virus infected mice

Diabetologia
|March 1, 1980
PubMed

Insights

Encephalomyocarditis virus infection causes diabetes in male mice. Testosterone exacerbates this effect, while castration offers protection against viral diabetes.

Area of Science:

  • Virology
  • Endocrinology
  • Immunology

Background:

  • Encephalomyocarditis virus (EMCV) M variant infection in DBA/2 mice can induce a diabetes mellitus-like condition.
  • This diabetogenic effect is predominantly observed in male mice, with females rarely exhibiting hyperglycemia.
  • The role of sex hormones in modulating the diabetogenic impact of EMCV is not fully understood.

Purpose of the Study:

  • To investigate the influence of testosterone on the development of EMCV-induced diabetes in male DBA/2 mice.
  • To elucidate the mechanisms underlying sex-based differences in susceptibility to viral diabetes.

Main Methods:

  • Adult male DBA/2 mice were divided into three groups: castrates, castrates treated with testosterone, and sham-operated controls.
  • All groups were infected with the M variant of EMCV.
  • Pancreatic insulin concentrations and blood glucose levels (hyperglycemia) were measured post-infection.

Main Results:

  • Infection led to a significant decrease in pancreatic insulin to approximately 10% of control values in intact males and testosterone-treated castrates.
  • Hyperglycemia was observed concurrently with reduced insulin levels in intact males and testosterone-treated castrates.
  • Untreated castrates showed a less pronounced reduction in pancreatic insulin and did not develop hyperglycemia.

Conclusions:

  • Testosterone plays a crucial role in exacerbating the diabetogenic effects of EMCV infection in male mice.
  • Castration appears to confer protection against the development of viral diabetes by mitigating the impact on pancreatic insulin.
  • These findings highlight the interplay between viral infections, sex hormones, and metabolic dysregulation in diabetes pathogenesis.

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