SCHIZOPHRENIC-PATIENTS TREATED WITH HIGH-DOSE PHENOTHIAZINE OR THIOXANTHENE BECOME DEFICIENT IN POLYUNSATURATED FATTY-ACIDS IN THEIR THROMBOCYTES

被引:17
作者
FISCHER, S
KISSLING, W
KUSS, HJ
机构
[1] TECH UNIV MUNICH,DEPT PSYCHIAT,W-8000 MUNICH 2,GERMANY
[2] UNIV MUNICH,DEPT PSYCHIAT,W-8000 MUNICH 2,GERMANY
关键词
D O I
10.1016/0006-2952(92)90015-B
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Total fatty acids were analysed in thrombocytes of schizophrenic patients treated with a "high dose" or "low dose" monotherapy of neuroleptic drugs phenothiazine or thioxanthene. The ratio of the very long chain fatty acid hexacosanoic acid to the long chain fatty acid docosanoic acid (C26:0/C22:0) increased in the "high dose" and "low dose" groups as compared to healthy untreated controls (P < 0.05). The polyunsaturated fatty acid arachidonic acid decreased in the "high" and "low dose" groups (P < 0.01 and P < 0.05). The polyunsaturated fatty acids alpha-linolenic acid, eicosapentaenoic acid and docosahexaenoic acid were not detectable in most of the "high dose" schizophrenic patients, however, they were found in the "low dose" group and in the controls. There was a negative correlation between the daily dosage of phenothiazine and the percentages of the polyunsaturated fatty acids arachidonic acid and alpha-linolenic acid + eicosapentaenoic acid + docosahexaenoic acid in thrombocytes (r = -0.87, P < 0.01 and r = -0.81, P < 0.01). Two patients of the "high dose" group with an especially high and long lasting monotherapy of neuroleptics were nearly devoid of polyunsaturated fatty acids in their thrombocytes. Untreated schizophrenic patients exhibited a fatty acid pattern in their thrombocytes not markedly different from that of the healthy untreated control group. We conclude that neuroleptic drugs phenothiazine or thioxanthene can alter the fatty acid pattern of thrombocytes.
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页码:317 / 323
页数:7
相关论文
共 10 条
[1]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[2]   THROMBOXANES - NEW GROUP OF BIOLOGICALLY-ACTIVE COMPOUNDS DERIVED FROM PROSTAGLANDIN ENDOPEROXIDES [J].
HAMBERG, M ;
SVENSSON, J ;
SAMUELSSON, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (08) :2994-2998
[3]   PEROXISOMAL FATTY-ACID OXIDATION IS SELECTIVELY INHIBITED BY PHENOTHIAZINES IN ISOLATED HEPATOCYTES [J].
LEIGHTON, F ;
PERSICO, R ;
NECOCHEA, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 120 (02) :505-511
[4]   THE CEREBROHEPATORENAL (ZELLWEGER) SYNDROME - INCREASED LEVELS AND IMPAIRED DEGRADATION OF VERY-LONG-CHAIN FATTY-ACIDS AND THEIR USE IN PRENATAL-DIAGNOSIS [J].
MOSER, AE ;
SINGH, I ;
BROWN, FR ;
SOLISH, GI ;
KELLEY, RI ;
BENKE, PJ ;
MOSER, HW .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (18) :1141-1146
[5]   IDENTIFICATION OF FEMALE CARRIERS OF ADRENOLEUKODYSTROPHY [J].
MOSER, HW ;
MOSER, AE ;
TROJAK, JE ;
SUPPLEE, SW .
JOURNAL OF PEDIATRICS, 1983, 103 (01) :54-59
[6]   LIPID-METABOLISM IN ZELLWEGERS SYNDROME [J].
POULOS, A .
PROGRESS IN LIPID RESEARCH, 1989, 28 (01) :35-51
[7]   SHORT AND LONG-TERM INFLUENCE OF PHENOTHIAZINES ON LIVER PEROXISOMAL FATTY-ACID OXIDATION IN RODENTS [J].
VANDENBRANDEN, C ;
VAMECQ, J ;
DACREMONT, G ;
PREMEREUR, N ;
ROELS, F .
FEBS LETTERS, 1987, 222 (01) :21-26
[8]   THIORIDAZINE - A SELECTIVE INHIBITOR OF PEROXISOMAL BETA-OXIDATION INVIVO [J].
VANDENBRANDEN, C ;
ROELS, F .
FEBS LETTERS, 1985, 187 (02) :331-333
[9]   EXPERIMENTAL INHIBITION OF PEROXISOMAL BETA-OXIDATION IN RATS - INFLUENCE ON BRAIN MYELINATION [J].
VANDENBRANDEN, C ;
LEEMAN, J ;
DACREMONT, G ;
COLLUMBIEN, R ;
ROELS, F .
GLIA, 1990, 3 (06) :458-463
[10]  
VONSCHACKY C, 1985, J LIPID RES, V26, P457