Therapy with interferon-beta modulates endogenous catecholamines in lymphocytes of patients with multiple sclerosis

Exp Neurol. 2008 Dec;214(2):315-21. doi: 10.1016/j.expneurol.2008.08.015. Epub 2008 Sep 12.

Abstract

Objective: To investigate the endogenous dopaminergic/adrenergic system of lymphocytes in multiple sclerosis (MS) patients during treatment with interferon (IFN)-beta.

Methods: Patients with relapsing-remitting MS undergoing IFN-beta treatment were prospectively studied during the first year of treatment. Circulating lymphocytes were obtained at baseline and after 1, 3, 6 and 12 months of treatment and assayed for catecholamine (CA) production and mRNA expression of tyrosine hydroxylase (TH, the rate-limiting enzyme in the synthesis of CA), beta(2)-adrenoceptors (AR) and D2, D3 and D5 dopaminergic receptors (DR).

Results: In cells from patients treated with IFN-beta for 12 months the production of CA hugely increased and was less sensitive to IFN-gamma-induced inhibition. Expression of mRNA for TH, beta(2)-AR and DRD5 was already enhanced after 1 month and further increased up to 6-12 months of treatment. On the contrary, DRD2 mRNA progressively decreased and DRD3 mRNA did not significantly change over the whole study period.

Conclusions: In MS patients IFN-beta treatment enhances the ability of lymphocytes to produce CA, and induces extensive modifications of both beta(2)-AR and DR-operated pathways. The clinical relevance of these effects deserves consideration.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Catecholamines / metabolism*
  • Cells, Cultured
  • Female
  • Humans
  • Immunologic Factors / administration & dosage*
  • Interferon-beta / administration & dosage*
  • Lymphocytes / cytology
  • Lymphocytes / drug effects*
  • Lymphocytes / metabolism
  • Male
  • Multiple Sclerosis, Relapsing-Remitting / drug therapy*
  • Multiple Sclerosis, Relapsing-Remitting / immunology*
  • Prospective Studies
  • Receptors, Adrenergic, beta-2 / genetics
  • Receptors, Dopamine D2 / genetics
  • Receptors, Dopamine D3 / genetics
  • Receptors, Dopamine D5 / genetics
  • Tyrosine 3-Monooxygenase / genetics
  • Young Adult

Substances

  • Catecholamines
  • Immunologic Factors
  • Receptors, Adrenergic, beta-2
  • Receptors, Dopamine D2
  • Receptors, Dopamine D3
  • Receptors, Dopamine D5
  • Interferon-beta
  • Tyrosine 3-Monooxygenase