Differential pharmacological regulation of drug efflux and pharmacoresistant schizophrenia

被引:22
作者
Bebawy, Mary [1 ]
Chetty, Manoranjenni [1 ]
机构
[1] Univ Sydney, Fac Pharm, Sydney, NSW 2006, Australia
关键词
D O I
10.1002/bies.20706
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pharmacoresistant schizophrenia is a significant impediment to the successful management of the disease. The expression and function of P-glycoprotein (P-gp) has recently been implicated in this phenomenon. P-gp is a multidrug efflux transporter that prevents drug substrates from crossing the blood-brain barrier (BBB). Although the direct interaction between individual antipsychotic agents and P-gp has been demonstrated, the effect of antipsychotic drug combinations used in disease management on P-gp transport function remains to be elucidated. This could have important clinical implications in some individuals as dosage adjustments based on plasma drug concentration changes may not always be appropriate if drug-drug interactions and the resulting changes in drug concentration in the brain are not considered. This paper introduces the potential impact that combination antipsychotic therapy may have on P-gp function at the BBB and discusses the consequences of this in the prevention and circumvention of unfavourable therapeutic response in schizophrenic disorders.
引用
收藏
页码:183 / 188
页数:6
相关论文
共 60 条
  • [1] ANNE K, 2003, CURRENT OPINION PSYC, V16, P713
  • [2] Pharmacogenetics and pharmacogenomics of schizophrenia: a review of last decade of research
    Arranz, M. J.
    de Leon, J.
    [J]. MOLECULAR PSYCHIATRY, 2007, 12 (08) : 707 - 747
  • [3] EXPRESSION OF P-GLYCOPROTEIN IN HIGH-GRADE OSTEOSARCOMAS IN RELATION TO CLINICAL OUTCOME
    BALDINI, N
    SCOTLANDI, K
    BARBANTIBRODANO, G
    MANARA, MC
    MAURICI, D
    BACCI, G
    BERTONI, F
    PICCI, P
    SOTTILI, S
    CAMPANACCI, M
    SERRA, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (21) : 1380 - 1385
  • [4] Selective modulation of P-glycoprotein-mediated drug resistance
    Bebawy, M
    Morris, MB
    Roufogalis, BD
    [J]. BRITISH JOURNAL OF CANCER, 2001, 85 (12) : 1998 - 2003
  • [5] BECK WT, 1986, CANCER RES, V46, P778
  • [6] In vitro P-glycoprotein affinity for atypical and conventional antipsychotics
    Boulton, DW
    DeVane, CL
    Liston, HL
    Markowitz, JS
    [J]. LIFE SCIENCES, 2002, 71 (02) : 163 - 169
  • [7] BOZINA N, 2006, J PSYCHIAT RES, V17
  • [8] Drug-metabolizing enzymes and therapeutic drug monitoring in psychiatry
    Brosen, K
    [J]. THERAPEUTIC DRUG MONITORING, 1996, 18 (04) : 393 - 396
  • [9] IMMUNOHISTOCHEMICAL DETECTION OF P-GLYCOPROTEIN - PROGNOSTIC CORRELATION IN SOFT-TISSUE SARCOMA OF CHILDHOOD
    CHAN, HSL
    THORNER, PS
    HADDAD, G
    LING, V
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (04) : 689 - 704
  • [10] P-GLYCOPROTEIN EXPRESSION AS A PREDICTOR OF THE OUTCOME OF THERAPY FOR NEUROBLASTOMA
    CHAN, HSL
    HADDAD, G
    THORNER, PS
    DEBOER, G
    LIN, YP
    ONDRUSEK, N
    YEGER, H
    LING, V
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (23) : 1608 - 1614