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精神药物对体外血小板膜物理性质的影响。

Effects of psychotropic agents on the physical properties of platelet membranes in vitro.

作者信息

Zubenko G S, Cohen B M

出版信息

Psychopharmacology (Berl). 1985;86(3):369-73. doi: 10.1007/BF00432231.

Abstract

Normal platelet membranes were exposed in vitro to a variety of psychotropic medications commonly used in the treatment of patients with psychiatric disorders. Changes in structural order at the hydrocarbon region of the drug-exposed membranes were determined by steady-state fluorescence polarization measurements employing the fluorescent probe 1,6-diphenyl-1,3,5-hexatriene (DPH). Chlorpromazine, an aliphatic phenothiazine, produced a significant increase in DPH fluorescence polarization at concentrations from 2-200 microM. Thioridazine, a piperidine phenothiazine, and three piperazine derivatives, perphenazine, trifluoperazine, and fluphenazine, produced significant increases in this parameter at concentrations from 20-200 microM. The other agents tested, including thiothixene, lithium, antidepressants, anxiolytics, and anticonvulsants, were without effect in the concentration ranges examined. The phenothiazine-induced increase in DPH fluorescence polarization apparently depended on the structure of the phenothiazine nucleus; changes in side-chain structure appeared to modulate this effect, most likely by altering the inherent membrane solubility of the agents.

摘要

将正常血小板膜在体外暴露于常用于治疗精神疾病患者的多种精神药物中。使用荧光探针1,6 - 二苯基 - 1,3,5 - 己三烯(DPH)通过稳态荧光偏振测量来确定药物暴露膜烃区域的结构有序变化。氯丙嗪,一种脂肪族吩噻嗪,在2 - 200微摩尔浓度范围内使DPH荧光偏振显著增加。硫利达嗪,一种哌啶吩噻嗪,以及三种哌嗪衍生物,奋乃静、三氟拉嗪和氟奋乃静,在20 - 200微摩尔浓度范围内使该参数显著增加。所测试的其他药物,包括替沃噻吨、锂、抗抑郁药、抗焦虑药和抗惊厥药,在所研究的浓度范围内均无作用。吩噻嗪引起的DPH荧光偏振增加显然取决于吩噻嗪核的结构;侧链结构的变化似乎调节了这种作用,最有可能是通过改变药物的固有膜溶解度来实现的。

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