Therapeutic benefits of the methyl donor S-adenosylmethionine on nerve injury-induced mechanical hypersensitivity and cognitive impairment in mice

Stéphanie Grégoire, Magali Millecamps, Lina Naso, Sonia Do Carmo, A. Claudio Cuello, Moshe Szyf, Laura S. Stone

Research output: Contribution to journalArticlepeer-review

16 Scopus citations


Despite considerable advances in understanding mechanisms involved in chronic pain, effective treatment remains elusive. Comorbid conditions including anxiety, depression, and cognitive impairment further impact quality of life. Chronic pain is associated with reversible changes in brain anatomy and function and with long-term changes in gene expression. Epigenetic mechanisms, including DNA methylation, contribute to wide-spread and long-lasting reprogramming of gene expression. We previously reported decreases in global DNA methylation in the mouse frontal cortex 6 months after induction of neuropathic pain using the spared nerve injury (SNI) model. Here, we examined the therapeutic effect of increasing DNA methylation using the methyl donor S-adenosylmethionine (SAM). S-adenosylmethionine is marketed as a nutritional supplement for a range of conditions including liver disease, depression, osteoarthritis, fibromyalgia, and dementia. Three months after SNI or sham surgery, animals were treated with SAM (20 mg/kg, 3×/week) or saline orally for 4 months, and the impact on sensory, motor, motivational, and cognitive indices was measured. S-adenosylmethionine attenuated SNI-induced mechanical hypersensitivity and reduced active avoidance of mechanical stimuli but had no effect on cold sensitivity or motor capacity. S-adenosylmethionine completely blocked nerve injury-induced cognitive impairment and attenuated SNI-induced decreases in global DNA methylation in the frontal cortex. In summary, chronic oral administration of the methyl donor, SAM, attenuated sensory and cognitive symptoms associated with nerve injury in mice. These effects may be mediated, in part, through modulation of DNA methylation in the central nervous system by systemic administration of the methyl donor SAM.

Original languageEnglish (US)
Pages (from-to)802-810
Number of pages9
Issue number5
StatePublished - May 1 2017
Externally publishedYes

Bibliographical note

Funding Information:
Supported by a grant from Pfizer Canada to L. S. Stone and M. Szyf, a grant from the Canadian Institutes for Health Research to L. S. Stone, M. Szyf, and M. Millecamps and a Louise and Alan Edwards Foundation Postdoctoral Fellowship to S. Grégoire.


  • Animal model
  • Cognitive impairment
  • DNA methylation
  • Epigenetics
  • Nutritional supplement


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