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本文引用的文献

1
Immunohistochemical localization of P-glycoprotein in rat brain and detection of its increased expression by seizures are sensitive to fixation and staining variables.大鼠脑中P-糖蛋白的免疫组织化学定位及其癫痫发作后表达增加的检测对固定和染色变量敏感。
J Histochem Cytochem. 2005 Apr;53(4):517-31. doi: 10.1369/jhc.4A6451.2005.
2
Pharmacoresistance and expression of multidrug transporter P-glycoprotein in kindled rats.点燃大鼠的药物抗性与多药转运体P-糖蛋白的表达
Neuroreport. 2004 Jul 19;15(10):1657-61. doi: 10.1097/01.wnr.0000134840.10390.a4.
3
The neurobiology of antiepileptic drugs for the treatment of nonepileptic conditions.用于治疗非癫痫性疾病的抗癫痫药物的神经生物学。
Nat Med. 2004 Jul;10(7):685-92. doi: 10.1038/nm1074.
4
Anti-HIV drug distribution to the central nervous system.抗HIV药物向中枢神经系统的分布。
Curr Pharm Des. 2004;10(12):1313-24. doi: 10.2174/1381612043384835.
5
ABC transporters and the blood-brain barrier.ABC转运蛋白与血脑屏障。
Curr Pharm Des. 2004;10(12):1295-312. doi: 10.2174/1381612043384844.
6
Expression, up-regulation, and transport activity of the multidrug-resistance protein Abcg2 at the mouse blood-brain barrier.多药耐药蛋白Abcg2在小鼠血脑屏障处的表达、上调及转运活性
Cancer Res. 2004 May 1;64(9):3296-301. doi: 10.1158/0008-5472.can-03-2033.
7
Inhibition of multidrug transporters by verapamil or probenecid does not alter blood-brain barrier penetration of levetiracetam in rats.维拉帕米或丙磺舒对多药转运体的抑制作用不会改变大鼠体内左乙拉西坦的血脑屏障通透性。
Epilepsy Res. 2004 Feb;58(2-3):85-91. doi: 10.1016/j.eplepsyres.2003.12.007.
8
St. John's Wort (Hypericum perforatum) induces overexpression of multidrug resistance protein 2 (MRP2) in rats: a 30-day ingestion study.圣约翰草(贯叶连翘)诱导大鼠多药耐药蛋白2(MRP2)过表达:一项为期30天的摄入研究。
Food Chem Toxicol. 2004 Jun;42(6):995-1002. doi: 10.1016/j.fct.2004.02.012.
9
Expression and cellular distribution of multidrug resistance-related proteins in the hippocampus of patients with mesial temporal lobe epilepsy.内侧颞叶癫痫患者海马中多药耐药相关蛋白的表达及细胞分布
Epilepsia. 2004 May;45(5):441-51. doi: 10.1111/j.0013-9580.2004.57703.x.
10
Multidrug resistance proteins in rheumatoid arthritis, role in disease-modifying antirheumatic drug efficacy and inflammatory processes: an overview.类风湿关节炎中的多药耐药蛋白、在改善病情抗风湿药疗效及炎症过程中的作用:综述
Scand J Rheumatol. 2003;32(6):325-36. doi: 10.1080/03009740310004333.

血脑屏障主动外排转运体:ATP结合盒基因家族。

Blood-brain barrier active efflux transporters: ATP-binding cassette gene family.

作者信息

Löscher Wolfgang, Potschka Heidrun

机构信息

Department of Pharmacology, Toxicology, and Pharmacy, University of Veterinary Medicine Hannover, Hannover D-30559, Germany.

出版信息

NeuroRx. 2005 Jan;2(1):86-98. doi: 10.1602/neurorx.2.1.86.

DOI:10.1602/neurorx.2.1.86
PMID:15717060
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC539326/
Abstract

The blood-brain barrier (BBB) contributes to brain homeostasis by protecting the brain from potentially harmful endogenous and exogenous substances. BBB active drug efflux transporters of the ATP-binding cassette (ABC) gene family are increasingly recognized as important determinants of drug distribution to, and elimination from, the CNS. The ABC efflux transporter P-glycoprotein (Pgp) has been demonstrated as a key element of the BBB that can actively transport a huge variety of lipophilic drugs out of the brain capillary endothelial cells that form the BBB. In addition to Pgp, other ABC efflux transporters such as members of the multidrug resistance protein (MRP) family and breast cancer resistance protein (BCRP) seem to contribute to BBB function. Consequences of ABC efflux transporters in the BBB include minimizing or avoiding neurotoxic adverse effects of drugs that otherwise would penetrate into the brain. However, ABC efflux transporters may also limit the central distribution of drugs that are beneficial to treat CNS diseases. Furthermore, neurological disorders such as epilepsy may be associated with overexpression of ABC efflux transporters at the BBB, resulting in pharmacoresistance to therapeutic medication. Therefore, modulation of ABC efflux transporters at the BBB forms a novel strategy to enhance the penetration of drugs into the brain and may yield new therapeutic options for drug-resistant CNS diseases.

摘要

血脑屏障(BBB)通过保护大脑免受潜在有害的内源性和外源性物质的影响,有助于维持大脑的内环境稳定。ATP结合盒(ABC)基因家族的血脑屏障活性药物外排转运蛋白越来越被认为是药物在中枢神经系统(CNS)分布和消除的重要决定因素。ABC外排转运蛋白P-糖蛋白(Pgp)已被证明是血脑屏障的关键元件,它可以将大量亲脂性药物主动转运出构成血脑屏障的脑毛细血管内皮细胞。除了Pgp,其他ABC外排转运蛋白,如多药耐药蛋白(MRP)家族成员和乳腺癌耐药蛋白(BCRP),似乎也对血脑屏障功能有贡献。血脑屏障中ABC外排转运蛋白的作用包括将那些原本会渗透进入大脑的药物的神经毒性不良反应降至最低或避免。然而,ABC外排转运蛋白也可能限制对治疗中枢神经系统疾病有益的药物在中枢的分布。此外,癫痫等神经系统疾病可能与血脑屏障处ABC外排转运蛋白的过度表达有关,导致对治疗药物产生耐药性。因此,调节血脑屏障处的ABC外排转运蛋白形成了一种增强药物脑内渗透的新策略,并可能为耐药性中枢神经系统疾病带来新的治疗选择。