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抗惊厥药物对人淋巴细胞外周苯二氮䓬受体的影响。

Effect of anticonvulsant drugs on peripheral benzodiazepine receptors of human lymphocytes.

作者信息

Ferrarese C, Marzorati C, Perego M, Bianchi G, Cavarretta R, Pierpaoli C, Moretti G, Frattola L

机构信息

Department of Neurology, University of Milan, Ospedale San Gerardo, Monza, Italy.

出版信息

Neuropharmacology. 1995 Apr;34(4):427-31. doi: 10.1016/0028-3908(95)00001-m.

Abstract

Anticonvulsant drugs, such as carbamazepine, may exert some of their effects through peripheral benzodiazepine receptors (PBR), which are present in glial cells and regulate the synthesis of neurosteroids. PBR have also been demonstrated in human lymphocytes, where they might be used as peripheral markers of anticonvulsant drug effects. In the present paper we investigated the interaction of various antiepileptic drugs with PBR of human lymphocytes and evaluated possible effects of acute and chronic treatment with these drugs. At normal therapeutic concentrations, diazepam, carbamazepine and phenobarbital occupy respectively 70, 30 and 10% of PBR sites in human lymphocytes. Although no change of receptor density or affinity was observed after acute in vitro treatment, in epileptic patients chronically treated with carbamazepine, phenobarbital and valproic acid, PBR Bmax was increased with respect to controls and untreated epileptics. Since PBR of human lymphocytes may be affected by anticonvulsant drug treatment, we suggest that they might be involved in the immunological alterations reported in these patients and might be used as peripheral markers of drug effects on the central nervous system.

摘要

抗惊厥药物,如卡马西平,可能通过外周苯二氮䓬受体(PBR)发挥其部分作用,该受体存在于神经胶质细胞中并调节神经甾体的合成。PBR在人类淋巴细胞中也有发现,在那里它们可能被用作抗惊厥药物作用的外周标志物。在本文中,我们研究了各种抗癫痫药物与人类淋巴细胞PBR的相互作用,并评估了这些药物急性和慢性治疗的可能效果。在正常治疗浓度下,地西泮、卡马西平和苯巴比妥分别占据人类淋巴细胞中PBR位点的70%、30%和10%。虽然急性体外治疗后未观察到受体密度或亲和力的变化,但在长期接受卡马西平、苯巴比妥和丙戊酸治疗的癫痫患者中,相对于对照组和未治疗的癫痫患者,PBR的最大结合容量(Bmax)增加。由于人类淋巴细胞的PBR可能受抗惊厥药物治疗的影响,我们认为它们可能与这些患者中报道的免疫改变有关,并且可能被用作药物对中枢神经系统作用的外周标志物。

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