RLIP76, a non-ABC transporter, and drug resistance in epilepsy

<p>Abstract</p> <p>Background</p> <p>Permeability of the blood-brain barrier is one of the factors determining the bioavailability of therapeutic drugs and resistance to chemically different antiepileptic drugs is a consequence of decreased intracerebral accumulation. T...

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Main Authors: Awasthi Yogesh C, Cucullo Luca, Singhal Sharad S, Fazio Vince, Hallene Kerri L, Awasthi Sanjay, Dini Gabriele, Janigro Damir
Format: Article
Language:English
Published: BMC 2005-09-01
Series:BMC Neuroscience
Online Access:http://www.biomedcentral.com/1471-2202/6/61
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author Awasthi Yogesh C
Cucullo Luca
Singhal Sharad S
Fazio Vince
Hallene Kerri L
Awasthi Sanjay
Dini Gabriele
Janigro Damir
author_facet Awasthi Yogesh C
Cucullo Luca
Singhal Sharad S
Fazio Vince
Hallene Kerri L
Awasthi Sanjay
Dini Gabriele
Janigro Damir
author_sort Awasthi Yogesh C
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Permeability of the blood-brain barrier is one of the factors determining the bioavailability of therapeutic drugs and resistance to chemically different antiepileptic drugs is a consequence of decreased intracerebral accumulation. The ABC transporters, particularly P-glycoprotein, are known to play a role in antiepileptic drug extrusion, but are not by themselves sufficient to fully explain the phenomenon of drug-resistant epilepsy. Proteomic analyses of membrane protein differentially expressed in epileptic foci brain tissue revealed the frequently increased expression of RLIP76/RALBP1, a recently described non-ABC multi-specific transporter. Because of a significant overlap in substrates between P-glycoprotein and RLIP76, present studies were carried out to determine the potential role of RLIP76 in AED transport in the brain.</p> <p>Results</p> <p>RLIP76 was expressed in brain tissue, preferentially in the lumenal surface of endothelial cell membranes. The expression was most prominent in blood brain barrier tissue from excised epileptic foci. Saturable, energy-dependent, anti-gradient transport of both phenytoin and carbamazepine were demonstrated using recombinant RLIP76 reconstituted into artificial membrane liposomes. Immunotitration studies of transport activity in crude membrane vesicles prepared from whole-brain tissue endothelium showed that RLIP76 represented the dominant transport mechanism for both drugs. RLIP76<sup>-/- </sup>knockout mice exhibited dramatic toxicity upon phenytoin administration due to decreased drug extrusion mechanisms at the blood-brain barrier.</p> <p>Conclusion</p> <p>We conclude that RLIP76 is the predominant transporter of AED in the blood brain barrier, and that it may be a transporter involved in mechanisms of drug-resistant epilepsy.</p>
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spelling doaj.art-bdf8f5c933ea44de971aaa9be7cde88b2022-12-22T02:50:07ZengBMCBMC Neuroscience1471-22022005-09-01616110.1186/1471-2202-6-61RLIP76, a non-ABC transporter, and drug resistance in epilepsyAwasthi Yogesh CCucullo LucaSinghal Sharad SFazio VinceHallene Kerri LAwasthi SanjayDini GabrieleJanigro Damir<p>Abstract</p> <p>Background</p> <p>Permeability of the blood-brain barrier is one of the factors determining the bioavailability of therapeutic drugs and resistance to chemically different antiepileptic drugs is a consequence of decreased intracerebral accumulation. The ABC transporters, particularly P-glycoprotein, are known to play a role in antiepileptic drug extrusion, but are not by themselves sufficient to fully explain the phenomenon of drug-resistant epilepsy. Proteomic analyses of membrane protein differentially expressed in epileptic foci brain tissue revealed the frequently increased expression of RLIP76/RALBP1, a recently described non-ABC multi-specific transporter. Because of a significant overlap in substrates between P-glycoprotein and RLIP76, present studies were carried out to determine the potential role of RLIP76 in AED transport in the brain.</p> <p>Results</p> <p>RLIP76 was expressed in brain tissue, preferentially in the lumenal surface of endothelial cell membranes. The expression was most prominent in blood brain barrier tissue from excised epileptic foci. Saturable, energy-dependent, anti-gradient transport of both phenytoin and carbamazepine were demonstrated using recombinant RLIP76 reconstituted into artificial membrane liposomes. Immunotitration studies of transport activity in crude membrane vesicles prepared from whole-brain tissue endothelium showed that RLIP76 represented the dominant transport mechanism for both drugs. RLIP76<sup>-/- </sup>knockout mice exhibited dramatic toxicity upon phenytoin administration due to decreased drug extrusion mechanisms at the blood-brain barrier.</p> <p>Conclusion</p> <p>We conclude that RLIP76 is the predominant transporter of AED in the blood brain barrier, and that it may be a transporter involved in mechanisms of drug-resistant epilepsy.</p>http://www.biomedcentral.com/1471-2202/6/61
spellingShingle Awasthi Yogesh C
Cucullo Luca
Singhal Sharad S
Fazio Vince
Hallene Kerri L
Awasthi Sanjay
Dini Gabriele
Janigro Damir
RLIP76, a non-ABC transporter, and drug resistance in epilepsy
BMC Neuroscience
title RLIP76, a non-ABC transporter, and drug resistance in epilepsy
title_full RLIP76, a non-ABC transporter, and drug resistance in epilepsy
title_fullStr RLIP76, a non-ABC transporter, and drug resistance in epilepsy
title_full_unstemmed RLIP76, a non-ABC transporter, and drug resistance in epilepsy
title_short RLIP76, a non-ABC transporter, and drug resistance in epilepsy
title_sort rlip76 a non abc transporter and drug resistance in epilepsy
url http://www.biomedcentral.com/1471-2202/6/61
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