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

被引:45
|
作者
Zaffaroni, Mauro [2 ]
Marino, Franca [1 ,3 ]
Bombelli, Raffaella [1 ]
Rasini, Ernanuela [1 ]
Monti, Marta [1 ]
Ferrari, Marco [1 ]
Ghezzi, Angelo [2 ]
Comi, Giancarlo [2 ,4 ,5 ]
Lecchini, Sergio [1 ,3 ]
Cosentino, Marco [1 ,3 ]
机构
[1] Univ Insubria, Dept Clin Med, Sect Expt & Clin Pharmacol, Varese, VA, Italy
[2] Hosp S Antonio Abate, Multiple Sclerosis Ctr, Gallarate, VA, Italy
[3] Univ Insubria, Ctr Res Neurosci, Varese, VA, Italy
[4] Inst Sci, Dept Neurol, Milan, Italy
[5] Univ Vita Salute, Osped San Raffaele, Milan, Italy
关键词
Multiple sclerosis; Interferon beta; Lymphocytes; Catecholamines; Catecholamine receptors;
D O I
10.1016/j.expneurol.2008.08.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 rnRNA 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 I month and further increased up to 6-12 months of treatment. On the contrary, DRD2 mRNA progressively decreased and DRD3 rnRNA 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. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:315 / 321
页数:7
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