Hitzemann R, Mark C, Hirschowitz J, Garver D
Biol Psychiatry. 1985 Apr;20(4):397-407. doi: 10.1016/0006-3223(85)90042-3.
Recent studies have shown that patients with a schizophrenic-like illness have a significant deficit in erythrocyte ghost membrane (EGM) phosphatidylcholine (PC); patients with the most severe deficiency showed a marked decrease in Na+-Li+ counterflow activity (Hitzemann et al. 1984a and b). The present study was undertaken to see if the decrement in PC is associated with a decrease in phospholipid methylation activity. Phospholipid methylation in human EGMs is distinctly different from that in rat EGMs (Hirata and Axelrod 1980) in that the human activity is not Mg++-dependent, and apparent methyltransferase I activity is located in the external membrane surface. The patient population consisted of 20 DSM-III schizophrenics (SCZ), 13 DSM-III schizophreniform (SF) disorder patients, and 11 DSM-III manics (M). Twelve age- and sex-matched controls were used for the comparison group. Methylation activity was significantly decreased in all three patient groups, although the M group had significantly higher activity than the SF group. Twenty-four of the SCZ and SF patients entered a Li+ trial. The Li+ responder group (n = 8) showed significantly lower activity than the nonresponder group (n = 16). Overall, we conclude that the decrement in phospholipid methylation activity partially contributes to the decrement in PC levels.
最近的研究表明,患有精神分裂症样疾病的患者红细胞膜(EGM)磷脂酰胆碱(PC)存在显著缺陷;最严重缺乏的患者钠-锂逆向转运活性显著降低(希茨曼等人,1984a和b)。本研究旨在探讨PC的减少是否与磷脂甲基化活性的降低有关。人EGM中的磷脂甲基化与大鼠EGM中的明显不同(平田和阿克塞尔罗德,1980),因为人类的活性不依赖于镁离子,且表观甲基转移酶I活性位于外膜表面。患者群体包括20名符合《精神疾病诊断与统计手册》第三版(DSM-III)标准的精神分裂症患者(SCZ)、13名符合DSM-III标准的精神分裂症样(SF)障碍患者和11名符合DSM-III标准的躁狂症患者(M)。选取12名年龄和性别匹配的对照者作为比较组。所有三个患者组的甲基化活性均显著降低,尽管M组的活性显著高于SF组。24名SCZ和SF患者进入锂盐试验。锂盐反应者组(n = 8)的活性显著低于无反应者组(n = 16)。总体而言,我们得出结论,磷脂甲基化活性的降低部分导致了PC水平的降低。