INTERACTION BETWEEN ANTIDEPRESSANTS AND PHOSPHOINOSITIDE SIGNAL TRANSDUCTION SYSTEM IN HUMAN PLATELETS

被引:14
作者
REHAVI, M
JERUSHALEMI, Z
AVIV, A
LAOR, N
PODLISZEWSKI, E
KARP, L
SHAVIT, S
WEIZMAN, R
机构
[1] BEILINSON MED CTR,BASIL & GERALD FELSENSTEIN MED RES CTR,IL-49100 PETAH TIQWA,ISRAEL
[2] BEILINSON MED CTR,ROGOFF MED RES INST,IL-49100 PETAH TIQWA,ISRAEL
[3] ABARBANEL MENTAL HLTH CTR,BAT YAM,ISRAEL
[4] YALE CHILD STUDY CTR,TEL AVIV,ISRAEL
[5] TEL AVIV COMMUNITY MENTAL HLTH CTR,TEL AVIV,ISRAEL
[6] TEL AVIV UNIV,SACKLER FAC MED,DEPT PSYCHIAT,IL-69978 TEL AVIV,ISRAEL
[7] BEILINSON MED CTR,GEHA PSYCHIAT HOSP,SACKLER FAC MED,IL-49100 PETAH TIQWA,ISRAEL
关键词
D O I
10.1016/0006-3223(93)90276-J
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The present study was designed to evaluate the inhibitory effect of antidepressants on thrombin-induced phosphoinositide (PI) hydrolysis. Thrombin 5 units/ml induced a 100%-200% increase in platelet inositol phosphates (IPs) formation. This effect was inhibited in a dose-dependent manner by various heterocyclic antidepressants (IC50 40-170 mumol/L) The monoamine oxidase inhibitor, phenelzine, in concentrations up to 500 mumol/L, was devoid of inhibitory activity. The tricyclic antidepressants, (50 mumol/L) inhibited also thrombin-induced platelet aggregation by 32%-47%. No alteration in thrombin-induced IPs formation was detected in recovered major depressed patients (n = 15) maintained on clomipramine (75-150 mg/day). These results indicate that the heterocyclic antidepressants interfere with the thrombin-linked PI-signaling system. However, the inhibitory effect is achieved only in concentrations above the plasma concentrations obtained with therapeutic doses of these agents.
引用
收藏
页码:40 / 44
页数:5
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