Yao Jeffrey K, Thomas Elizabeth A, Reddy Ravinder D, Keshavan Matcheri S
Neurochemistry and Psychopharmacology Laboratory (Bldg. 13), VA Pittsburgh Healthcare System, 7180 Highland Dr., Pittsburgh, PA 15206, USA.
Schizophr Res. 2005 Jan 1;72(2-3):259-66. doi: 10.1016/j.schres.2004.05.007.
Apolipoprotein D (apoD) is a member of the lipocalin superfamily of transporter proteins that bind small hydrophobic molecules, including arachidonic acid (AA). The ability of apoD to bind AA implicates it in pathways associated with membrane phospholipid signal transduction and metabolism. Recent findings of an increased expression of apoD in the mouse brain after clozapine treatment suggested a role for apoD in the pharmacological action of clozapine. Moreover, clozapine has been shown to increase membrane AA levels in RBC phospholipids from schizophrenic patients. ApoD levels have also been shown to be elevated in the CNS of subjects with chronic schizophrenia, a disorder associated with AA dysfunction. In this study, we examined whether plasma apoD levels are related to red blood cell membrane AA contents in the first-episode neuroleptic-naive schizophrenic (FENNS) patients. Plasma apoD levels as measured by enzyme-linked immunosorbent assay (ELISA) were not significantly different (F = 0.51, df = 2,86, p = 0.60) among healthy controls (n = 36), FENNS patients (n = 33) and patients with other psychiatric disorders (n = 19). However, plasma apoD levels were significantly correlated with RBC-AA (p = 0.0022) and docosapentaenoic acid (p = 0.0008) in FENNS patients. There are several known mechanisms that can lead to the type of membrane fatty acid defects that have been identified in schizophrenia. Whether plasma apoD alone is a major determinant of reduced RBC membrane AA levels in FENNS patients remains to be determined, although these preliminary data appear not to support this premise. Taken together with other in vitro studies, however, the present data support the view that an increased expression of apoD such as induced by atypical neuroleptic drug, may facilitate incorporation of AA into membrane phospholipids by its selective binding to AA.
载脂蛋白D(apoD)是脂质运载蛋白超家族转运蛋白的成员,该家族蛋白可结合包括花生四烯酸(AA)在内的小疏水分子。apoD结合AA的能力表明其参与了与膜磷脂信号转导和代谢相关的途径。最近的研究发现,氯氮平治疗后小鼠脑中apoD的表达增加,提示apoD在氯氮平的药理作用中发挥作用。此外,已有研究表明氯氮平可增加精神分裂症患者红细胞磷脂中的膜AA水平。在患有慢性精神分裂症(一种与AA功能障碍相关的疾病)的受试者中枢神经系统中,apoD水平也已显示升高。在本研究中,我们检查了首发未使用过抗精神病药物的精神分裂症患者(FENNS)的血浆apoD水平是否与红细胞膜AA含量相关。通过酶联免疫吸附测定(ELISA)测得的血浆apoD水平在健康对照者(n = 36)、FENNS患者(n = 33)和其他精神疾病患者(n = 19)之间无显著差异(F = 0.51,自由度 = 2,86,p = 0.60)。然而,FENNS患者的血浆apoD水平与红细胞AA(p = 0.0022)和二十二碳五烯酸(p = 0.0008)显著相关。有几种已知机制可导致精神分裂症中已确定的膜脂肪酸缺陷类型。尽管这些初步数据似乎不支持这一前提,但血浆apoD本身是否是FENNS患者红细胞膜AA水平降低的主要决定因素仍有待确定。然而,结合其他体外研究,目前的数据支持这样一种观点,即非典型抗精神病药物诱导的apoD表达增加可能通过其与AA的选择性结合促进AA掺入膜磷脂中。