Cohen B M, Zubenko G S
Psychopharmacology (Berl). 1985;86(3):365-8. doi: 10.1007/BF00432230.
Marked changes in biophysical properties, including structural order, have been observed in the hydrophobic core of cell membranes exposed to phenothiazines in vitro. In this study, similar changes are reported in vivo in cell membranes from the brains of rats treated with phenothiazines at doses thought to yield tissue concentrations approximating those attained in the clinical treatment of psychiatric patients. The membrane structural order parameter was estimated ex vivo by steady-state fluorescence polarization determinations using 1,6-diphenyl 1,3,5-hexatriene (DPH), a fluorescent probe that localizes preferentially to the hydrocarbon region of cell membranes. In these preliminary studies, rats received chlorpromazine (20 mg/kg), fluphenazine (1 mg/kg), haloperidol (1 mg/kg), and imipramine (1 mg/kg) in single or multiple dose protocols. As in earlier in vitro studies, exposure to the phenothiazine antipsychotics led to an observed increase in DPH fluorescence polarization ex vivo and a presumed increase in structural order. As predicted from the in vitro experiments, the effect of chlorpromazine was greater than that of fluphenazine, probably because chlorpromazine was given at higher doses. The magnitude of the effects seen was great enough to imply that physiologically significant changes in cell membrane characteristics may be produced in patients receiving phenothiazines.
在体外,已观察到暴露于吩噻嗪类药物的细胞膜疏水核心的生物物理性质发生显著变化,包括结构有序性。在本研究中,据报道,用吩噻嗪类药物治疗的大鼠大脑细胞膜在体内也有类似变化,所用剂量被认为能使组织浓度接近精神病患者临床治疗时达到的浓度。使用1,6 - 二苯基 - 1,3,5 - 己三烯(DPH)通过稳态荧光偏振测定法离体估计膜结构有序参数,DPH是一种优先定位于细胞膜烃区域的荧光探针。在这些初步研究中,大鼠以单次或多次给药方案接受氯丙嗪(20毫克/千克)、氟奋乃静(1毫克/千克)、氟哌啶醇(1毫克/千克)和丙咪嗪(1毫克/千克)。与早期的体外研究一样,暴露于吩噻嗪类抗精神病药物导致离体观察到DPH荧光偏振增加以及推测的结构有序性增加。正如体外实验所预测的,氯丙嗪的作用大于氟奋乃静,可能是因为氯丙嗪的给药剂量更高。观察到的效应大小足以表明,接受吩噻嗪类药物治疗的患者细胞膜特性可能发生具有生理意义的变化。