Voluntary wheel running during adolescence distinctly alters running output in adulthood in male and female rats

Behav Brain Res. 2020 Jan 13:377:112235. doi: 10.1016/j.bbr.2019.112235. Epub 2019 Sep 12.

Abstract

Adult female rats show greater running output compared with age-matched male rats, and the midbrain dopaminergic system may account for behavioral differences in running output. However, it is unknown if the lower running output in adult males can be regulated by wheel running experience during adolescence, and whether wheel running experience during adolescence will diminish the sex differences in running output during adulthood. We therefore determined and compared the exercise output in adult male and female rats that either had initiated voluntary wheel running only during adulthood or during adolescence. Our results demonstrate that running output in adult males were significantly higher when running was initiated during adolescence, and this higher running output was not significantly different from females. Running output did not differ during adulthood in females when wheel running was initiated during adolescence or during adulthood. Higher running output in females was associated with reduced expression of tyrosine hydroxylase and hyperactivation of calcium/calmodulin-dependent protein kinase II (CaMKII) in the dorsal striatum. Notably, running during adolescence-induced higher exercise output in adult males was associated with hyperactivation of CaMKII in the dorsal striatum, indicating a mechanistic role for CaMKII in running output. Together, the present results indicate sexually dimorphic adaptive biochemical changes in the dorsal striatum in rats that had escalated running activity, and highlight the importance of including sex as a biological variable in exploring neuroplasticity changes that predict enhanced exercise output in a voluntary physical activity paradigm.

Keywords: CaMKII; D1R; MAPK-1; PSD-95; Physical activity; Tyrosine hydroxylase.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Age Factors
  • Animals
  • Behavior, Animal / physiology*
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism*
  • Female
  • Male
  • Models, Animal
  • Neostriatum / metabolism*
  • Phosphorylation / physiology
  • Rats
  • Rats, Long-Evans
  • Running / physiology*
  • Sex Characteristics*
  • Tyrosine 3-Monooxygenase / metabolism*

Substances

  • Tyrosine 3-Monooxygenase
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2