Activation of Three Major Signaling Pathways After Endurance Training and Spinal Cord Injury

Mol Neurobiol. 2022 Feb;59(2):950-967. doi: 10.1007/s12035-021-02628-y. Epub 2021 Nov 22.

Abstract

We aimed to investigate the effects of endurance training on expression of growth factors (GFs) and stimulation of neurotrophin-dependent signaling pathways (PI3k/Akt, PLCγ/PKC, PLCγ/CAMKII, Ras-Erk1/2 and Rac1-Cdc42) responsible for neuroplasticity, neuroregeneration, survival and growth after spinal cord injury (SCI). Wistar rats were divided into four groups: (i) intact controls; (ii) 6 weeks of endurance training; (iii) SCI; (iv) pre-training + SCI. The animals survived for 6 weeks after SCI. Firstly, endurance training markedly upregulated mRNA expression and protein levels (up to four times) of growth factors (BDNF, GDNF) and their receptors (TrkB, Gfrα) in low thoracic segments (Th8-Th10) compared to levels in untrained animals. Secondly, we found that spontaneous neuroplasticity seen in the SCI alone group was GF-specific and was activated through both PLCγ-PKC and PLC-CAMKII signaling pathways. In addition, training prior to SCI markedly increased the activity of PLCγ-PKC signaling at both transcript and protein levels at and around the lesion site. Similar effects were seen in expression of PI3k/Akt and Ras/Erk1/2 signaling responsible for cell survival and regeneration. Thirdly, rats which underwent physical activity prior to SCI were more active and had significantly better neurological scores at the 14th and 42nd days of survival. These results suggest that regular physical activity could play an important role after SCI, as it maintains increased expression of GFs in spinal cord tissue 6 weeks post-SCI. The BDNF- and/or BDNF + GDNF-dependent signaling pathways were significantly affected in pre-trained SCI animals. In contrast, GDNF-dependent Rac1-Cdc42 signaling was not involved in training-affected SCI response.

Keywords: BDNF; GDNF; Neuroplasticity; Neurotrophin-dependent intracellular signaling; PLCγ-PKC pathway; Spinal cord compression.

MeSH terms

  • Animals
  • Brain-Derived Neurotrophic Factor / metabolism
  • Endurance Training*
  • MAP Kinase Signaling System
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phospholipase C gamma / metabolism
  • Protein Kinase C / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Proto-Oncogene Proteins p21(ras)
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Wistar
  • Recovery of Function
  • Signal Transduction* / physiology
  • Spinal Cord / pathology
  • Spinal Cord Injuries* / pathology

Substances

  • Brain-Derived Neurotrophic Factor
  • Proto-Oncogene Proteins c-akt
  • Protein Kinase C
  • Phospholipase C gamma
  • phospholipase Cgamma1, rat
  • Proto-Oncogene Proteins p21(ras)