Dynamics of ECT normalization of low G protein function and immunoreactivity in mononuclear leukocytes of patients with major depression

被引:29
作者
Avissar, S
Nechamkin, Y
Roitman, G
Schreiber, G
机构
[1] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Clin Pharmacol, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Psychiat, IL-84105 Beer Sheva, Israel
关键词
D O I
10.1176/ajp.155.5.666
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Heterotrimeric G proteins were Previously implicated in the biochemical mechanisms underlying the pathophysiology and treatment of mood disorders. Low function and immunoreactivity of G proteins were observed in patients with major depression. In the present study the authors evaluated the effects of ECT on the low measures of G proteins in patients with major depression. Method: Repented G protein measurements in mononuclear leukocytes of 10 patients with major depression were made. Each patient was examined while untreated and after successive sessions of ECT; 14 normal subjects were also studied. G protein function was evaluated through beta-adrenergic- and muscarinic-agonist-enhanced guanine nucleotide binding capacity, substantiated by quantitative measures of G proteins through immunoblot analyses using polyclonal antibodies against G(s) alpha, G(i) alpha, and G beta proteins. Results: Mononuclear leukocytes of patients with depression showed immunoreactive levels of G(s) alpha and G(i) alpha that were significantly lower than those of normal subjects; the depressed patients also had markedly hypofunctional G(s) and G(i). The low levels of G protein function and immunoreactivity were alleviated by ECT. Repeated measurements in the same patients after successive ECT sessions showed that the normalization of G protein measures preceded, and thus predicted, clinical improvement. The function and quantity of G(s) and G(i) proteins in patients given ECT were significantly correlated. Conclusions: These findings support the implication of G proteins in the pathophysiology and treatment of mood disorders. G protein measurements in patients with depression may potentially serve not only as a biochemical marker for affective state but also for biochemical prediction and evaluation of responses to ECT.
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页码:666 / 671
页数:6
相关论文
共 45 条
[1]   Measurement of early events in signal transduction beyond receptors involving G proteins function in mononuclear leucocytes [J].
Avissar, S ;
Schreiber, G .
JOURNAL OF NEUROIMMUNOLOGY, 1996, 70 (01) :81-86
[2]   INTERACTION OF ANTIBIPOLAR AND ANTIDEPRESSANT TREATMENTS WITH RECEPTOR-COUPLED G-PROTEINS [J].
AVISSAR, S ;
SCHREIBER, G .
PHARMACOPSYCHIATRY, 1992, 25 (01) :44-50
[3]   MAGNESIUM REVERSAL OF LITHIUM INHIBITION OF BETA-ADRENERGIC AND MUSCARINIC RECEPTOR COUPLING TO G-PROTEINS [J].
AVISSAR, S ;
MURPHY, DL ;
SCHREIBER, G .
BIOCHEMICAL PHARMACOLOGY, 1991, 41 (02) :171-175
[4]  
Avissar S, 1997, AM J PSYCHIAT, V154, P211
[5]   THE INVOLVEMENT OF GUANINE-NUCLEOTIDE BINDING-PROTEINS IN THE PATHOGENESIS AND TREATMENT OF AFFECTIVE-DISORDERS [J].
AVISSAR, S ;
SCHREIBER, G .
BIOLOGICAL PSYCHIATRY, 1992, 31 (05) :435-459
[6]   Reduced beta-adrenergic receptor-coupled Gs protein function and Gs alpha immunoreactivity in mononuclear leukocytes of patients with depression [J].
Avissar, S ;
BarkiHarrington, L ;
Nechamkin, Y ;
Roitman, G ;
Schreiber, G .
BIOLOGICAL PSYCHIATRY, 1996, 39 (09) :755-760
[7]   Differential G protein measures in mononuclear leukocytes of patients with bipolar mood disorder are state dependent [J].
Avissar, S ;
Nechamkin, Y ;
BarkiHarrington, L ;
Roitman, G ;
Schreiber, G .
JOURNAL OF AFFECTIVE DISORDERS, 1997, 43 (02) :85-93
[8]   BENNETT,AE AWARD PAPER MUSCARINIC RECEPTOR SUBCLASSIFICATION AND G-PROTEINS - SIGNIFICANCE FOR LITHIUM ACTION IN AFFECTIVE-DISORDERS AND FOR THE TREATMENT OF THE EXTRAPYRAMIDAL SIDE-EFFECTS OF NEUROLEPTICS [J].
AVISSAR, S ;
SCHREIBER, G .
BIOLOGICAL PSYCHIATRY, 1989, 26 (02) :113-130
[9]   LITHIUM INHIBITS ADRENERGIC AND CHOLINERGIC INCREASES IN GTP BINDING IN RAT CORTEX [J].
AVISSAR, S ;
SCHREIBER, G ;
DANON, A ;
BELMAKER, RH .
NATURE, 1988, 331 (6155) :440-442
[10]  
AVISSAR S, 1990, EUR J PHARM-MOLEC PH, V100, P99