Electrical stimulation and testosterone differentially enhance expression of regeneration-associated genes

Nijee Sharma, Sam J. Marzo, Kathryn J. Jones, Eileen M. Foecking

Research output: Contribution to journalArticle

50 Citations (Scopus)

Abstract

As functional recovery following peripheral nerve injury is dependent upon successful repair and regeneration, treatments that enhance different regenerative events may be advantageous. Using a rat facial nerve crush axotomy model, our lab has previously investigated the effects of a combinatorial treatment strategy, consisting of electrical stimulation (ES) of the proximal nerve stump and testosterone propionate (TP) administration. Results indicated that the two treatments differentially enhance facial nerve regenerative properties, whereby ES reduced the delay before sprout formation, TP accelerated the overall regeneration rate, and the combinatorial treatment had additive effects. To delineate the molecular mechanisms underlying such treatments, the present study investigated the effects of ES and TP on expression of specific regeneration-associated genes. Following a right facial nerve crush at the stylomastoid foramen, gonadectomized adult male rats were administered only ES, only TP, a combination of both, or left untreated. Real time RT-PCR analysis was used to assess fold changes in mRNA levels in the facial motor nucleus at 0 h, 6 h, 1 d, 2 d, 7 d, and 21 d post-axotomy. The candidate genes analyzed included two tubulin isoforms (α1-tubulin and βII-tubulin), 43-kiloDalton growth-associated protein (GAP-43), brain derived neurotrophic factor (BDNF), pituitary adenylate cyclase-activating peptide (PACAP), and neuritin (candidate plasticity-related gene 15). The two treatments have differential effects on gene expression, with ES leading to early but transient upregulation and TP producing late but steady increases in mRNA levels. In comparison to individual treatments, the combinatorial treatment strategy has the most enhanced effects on the transcriptional program activated following injury.

Original languageEnglish (US)
Pages (from-to)183-191
Number of pages9
JournalExperimental Neurology
Volume223
Issue number1
DOIs
StatePublished - May 1 2010

Fingerprint

Testosterone Propionate
Electric Stimulation
Testosterone
Regeneration
Facial Nerve
Tubulin
Nerve Crush
GAP-43 Protein
Axotomy
Genes
Peripheral Nerve Injuries
Messenger RNA
Brain-Derived Neurotrophic Factor
Adenylyl Cyclases
Real-Time Polymerase Chain Reaction
Protein Isoforms
Up-Regulation
Gene Expression
Peptides
Wounds and Injuries

Keywords

  • Electrical stimulation
  • Nerve injury
  • Regeneration
  • Regeneration-associated genes
  • Testosterone

ASJC Scopus subject areas

  • Neurology
  • Developmental Neuroscience

Cite this

Electrical stimulation and testosterone differentially enhance expression of regeneration-associated genes. / Sharma, Nijee; Marzo, Sam J.; Jones, Kathryn J.; Foecking, Eileen M.

In: Experimental Neurology, Vol. 223, No. 1, 01.05.2010, p. 183-191.

Research output: Contribution to journalArticle

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