Beneficial effects of dimethyl fumarate on experimental autoimmune myocarditis

Arch Med Res. 2008 Oct;39(7):639-46. doi: 10.1016/j.arcmed.2008.07.003.

Abstract

Background: Fumaric acid esters (FAE) have been proven to be effective for the systemic treatment of psoriasis and multiple sclerosis, Th1 cell-mediated chronic inflammatory diseases, but their effect on autoimmune myocarditis has not yet been addressed. We investigated the effect of dimethyl fumarate (DMF) on myosin-induced experimental autoimmune myocarditis (EAM).

Methods: Dark Agouti (DA) rats immunized with porcine cardiac myosin were orally treated with 5 and 15 mg/kg body weight (bw) DMF either from days 0-10 (early treatment groups) or from days 10-21 (late treatment groups) after induction of EAM. All rats were sacrificed on day 21 after immunization and hearts were evaluated macroscopically and microscopically. Levels of TNF-alpha and IL-10 in serum and lymph node cells culture supernatants were detected by ELISA.

Results: Both early and late treatment with 15 mg/kg body weight (bw) DMF markedly reduced the severity of myocarditis by comparing the incidence, heart weight/bw ratio, macroscopic and microscopic scores, and number of OX-6+ cells in the myocardium. Further, levels of tumor necrosis factor-alpha (TNF-alpha) in serum and culture supernatants of lymph node cells stimulated with ConA or myosin were significantly lower in DMF-treated EAM animals compared with vehicle-treated EAM rats. There was no significant difference in serum levels of interleukin-10 between DMF- and vehicle-treated EAM rats.

Conclusions: These results show for the first time that DMF ameliorates experimental autoimmune myocarditis and may be acted, at least in part, by interfering with the production of TNF-alpha.

MeSH terms

  • Animals
  • Autoimmune Diseases / drug therapy*
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / pathology
  • Dimethyl Fumarate
  • Disease Models, Animal
  • Fumarates / administration & dosage
  • Fumarates / therapeutic use*
  • Immunosuppressive Agents / administration & dosage
  • Immunosuppressive Agents / therapeutic use*
  • Interleukin-10 / blood
  • Interleukin-10 / metabolism
  • Lymphocytes / immunology*
  • Lymphocytes / metabolism
  • Male
  • Myocarditis / drug therapy*
  • Myocarditis / immunology
  • Myocarditis / pathology
  • Myocardium / pathology
  • Myosins / immunology
  • Rats
  • Tumor Necrosis Factor-alpha / blood
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Fumarates
  • Immunosuppressive Agents
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Myosins
  • Dimethyl Fumarate