Facilitation of drug entry into the CNS via transient permeation of blood brain barrier: laboratory and preliminary clinical evidence from bradykinin receptor agonist, Cereport

被引:105
作者
Borlongan, CV
Emerich, DF
机构
[1] Med Coll Georgia, Dept Neurol, Augusta, GA 30912 USA
[2] Med Coll Georgia, Inst Mol Med & Genet, Augusta, GA 30912 USA
[3] Med Coll Georgia, Sch Grad Studies, Augusta, GA 30912 USA
[4] Augusta Vet Adm Med Ctr, Res & Affiliat Serv Line, Augusta, GA 30912 USA
[5] Sertoli Technol Inc, Cranston, RI 02921 USA
关键词
BBB; chemotherapeutics; analgesics; immunosuppressants; brain tumor; pain; Parkinson's disease; neuroprotection;
D O I
10.1016/S0361-9230(03)00043-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
One novel approach of transporting drugs into the central nervous system (CNS) involves the activation of receptors on the endothelial cells comprising the blood brain barrier (BBB). Recently the selective B, bradykinin receptor agonist, Cereport (also called RMP-7), has been shown to transiently increase permeability of the BBB. Although initially developed to increase the permeability of the vasculature feeding glioma, recent studies have demonstrated that Cereport also increases the delivery of pharmacological agents across the normal (i.e. nontumor) BBB. In this review paper, we discuss evidence of enhanced CNS delivery of carboplatin, loperamide, and cyclosporin-A, which are accompanied by enhanced chemotherapeutic, analgesic and neuroprotective effects, respectively. These observations suggest feasibility of Cereport as an adjunct therapy to pharmacological treatments that require drug availability in the CNS to exert therapeutic efficacy. Because many potential drugs for CNS disorders normally do not cross the BBB, Cereport-induced transient permeation of BBB stands as an efficacious strategy for enhancing pharmacotherapy. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:297 / 306
页数:10
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