Physical exercise increases the production of tyrosine hydroxylase and CDNF in the spinal cord of a Parkinson's disease mouse model

Neurosci Lett. 2021 Aug 24:760:136089. doi: 10.1016/j.neulet.2021.136089. Epub 2021 Jun 26.

Abstract

Previous research advocates that exercise is a non-pharmacological therapy for Parkinson's disease (PD). However, few studies have investigated the effects of exercise on central nervous system structures other than the nigrostriatal pathway by using PD animal models. This study investigated the effects of exercise on tyrosine hydroxylase (TH)- and cerebral dopamine neurotrophic factor (CDNF)-containing spinal-cord neurons. Male Swiss mice were divided into 4 groups: sedentary control (SEDCONT), exercise control (EXERCONT), sedentary Parkinson (SEDPD), and exercise Parkinson (EXERPD). The PD groups were submitted to a surgical procedure for stereotaxic bilateral injection of 6-hydroxydopamine into the striatum. TH- and CDNF-containing spinal-cord neurons were evaluated in all groups, using immunohistochemistry and western-blotting. TH content in the ventral horn differed notably between the SEDPD and EXERPD groups. CDNF content was highest in the EXERPD group. SEDPD and EXERPD groups differed the most, as shown by immunohistochemistry and western-blotting. The EXERPD group showed the most intense labeling in immunohistochemistry compared to the SEDCONT and EXERCONT groups. Therefore, we showed here that exercise increased the content of both TH and CDNF in the spinal-cord neurons of a bilateral PD mouse model. We may assume that the spinal cord is affected in a PD model, and therefore this central nervous system region deserves more attention from researchers dealing with PD.

Keywords: Animal model; Cerebral dopamine neurotrophic factor; Exercise; Parkinson’s disease; Tyrosine hydroxylase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Corpus Striatum / metabolism
  • Disease Models, Animal
  • Humans
  • Male
  • Mice
  • Motor Neurons / metabolism*
  • Nerve Growth Factors / analysis
  • Nerve Growth Factors / metabolism*
  • Oxidopamine / metabolism
  • Parkinsonian Disorders / pathology
  • Parkinsonian Disorders / rehabilitation*
  • Spinal Cord / cytology
  • Spinal Cord / metabolism
  • Spinal Cord / pathology
  • Tyrosine 3-Monooxygenase / analysis
  • Tyrosine 3-Monooxygenase / metabolism*

Substances

  • Nerve Growth Factors
  • cdnf protein, mouse
  • Oxidopamine
  • Tyrosine 3-Monooxygenase