期刊
INTERNATIONAL JOURNAL OF PSYCHIATRY IN MEDICINE
卷 40, 期 4, 页码 413-424出版社
SAGE PUBLICATIONS INC
DOI: 10.2190/PM.40.4.e
关键词
amitriptyline; nortriptyline; imipramine; desipramine; venlafaxine; O-desmethylvenlafaxine; TSST-1; IFN-gamma
类别
Objective: A growing body of data indicates that an activation of pro-inflammatory cytokines such as interferon-gamma (IFN-gamma) is involved in the pathophysiology of depression and that the suppression of pro-inflammatory cytokine production by antidepressants may lead to an improvement of depressive symptoms. However, the influence of the serotornn and noradrenalin reuptake inhibitor (SNRI) venlafaxine and its metabolite O-desmethylvenlafaxine on the stimulated blood cell secretion of IFN-gamma has not been studied so far. Method: We measured IFN-gamma levels in the stimulated blood of healthy female subjects in a whole blood assay using the toxic shock syndrome toxin TSST-1 as stimulant. Blood was either supplemented with antidepressants or not. Results: Mean IFN-gamma concentrations differed between blood with and without antidepressant supplements (p = 0.026). Planned contrasts revealed that compared to non-supplemented blood, four of the blood samples supplemented with the tricyclic antidepressants (TCAs) reduced IFN-gamma levels: amitriptylinc (adjusted p-value (p = 0.004), nortriptyline (p = 0.037), imipramine (p = 0.021), and desipramine (p = 0.048). There was no significant difference between the control condition and the venlafaxine or O-desmethylvenlafaxine condition. Conclusions: TCAs might, among other mechanisms, act as antidepressants by suppressing the production of pro-inflammatory cytokines, whereas no significant effect of venlafaxine and O-desmethylvenlafaxine on IFN-y secretion could be demonstrated. (Int'l. J. Psychiatry in Medicine 2010;40:413-424)
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