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精神分裂症患者血小板磷脂酶A2活性增加。

Increased platelet phospholipase A2 activity in schizophrenia.

作者信息

Gattaz W F, Schmitt A, Maras A

机构信息

Neurobiology Unit, Central Institute of Mental Health, Mannheim, Germany.

出版信息

Schizophr Res. 1995 Jul;16(1):1-6. doi: 10.1016/0920-9964(94)00060-l.

Abstract

The intracellular enzyme phospholipase A2 (PLA2) plays an essential role in the breakdown of membrane phospholipids, which regulate the physicochemical properties of the cell membrane. In the brain PLA2 has been reported to influence receptor function and signal transduction. Regarding dopaminergic neurons, data from animals experiments and from binding studies suggest that PLA2 activation reduces dopaminergic neurotransmission. In the present study we investigated intracellular PLA2 in platelets from 31 DSM-III-R paranoid schizophrenic patients (15 neuroleptic-naive) compared to 31 healthy individuals and to 31 non-schizophrenic psychiatric controls, both matched to the schizophrenics by age and sex. Platelet PLA2 activity was significantly increased in schizophrenics as compared to healthy and to psychiatric controls. Neuroleptic treatment reduced significantly the enzyme activity. Our findings in platelets suggest an accelerated breakdown of membrane phospholipids in schizophrenia. An accelerated phospholipid breakdown has also been reported in the frontal cortex from schizophrenic patients. Further studies should clarify whether increased PLA2 in the brain, as observed in platelets, could contribute to a frontal dysfunction in schizophrenia.

摘要

细胞内酶磷脂酶A2(PLA2)在膜磷脂分解过程中发挥着重要作用,而膜磷脂可调节细胞膜的物理化学性质。据报道,在大脑中PLA2会影响受体功能和信号转导。关于多巴胺能神经元,动物实验和结合研究的数据表明,PLA2的激活会降低多巴胺能神经传递。在本研究中,我们调查了31名DSM-III-R偏执型精神分裂症患者(15名未使用过抗精神病药物)血小板中的细胞内PLA2,将其与31名健康个体以及31名非精神分裂症的精神科对照者进行比较,后两者在年龄和性别上与精神分裂症患者相匹配。与健康个体和精神科对照者相比,精神分裂症患者的血小板PLA2活性显著升高。抗精神病药物治疗显著降低了该酶的活性。我们在血小板中的研究结果表明,精神分裂症患者存在膜磷脂分解加速的情况。在精神分裂症患者的额叶皮质中也有磷脂分解加速的报道。进一步的研究应阐明,正如在血小板中观察到的那样,大脑中PLA2的增加是否可能导致精神分裂症患者的额叶功能障碍。

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