Yousif Salah, Saubaméa Bruno, Cisternino Salvatore, Marie-Claire Cynthia, Dauchy Sandrine, Scherrmann Jean-Michel, Declèves Xavier
CNRS, UMR 7157 et Université Paris 7, Neuropsychopharmacologie des addictions, Faculté des Sciences Pharmaceutiques et Biologiques, Université Paris Descartes, Paris, France.
J Neurochem. 2008 Nov;107(3):647-57. doi: 10.1111/j.1471-4159.2008.05647.x. Epub 2008 Aug 30.
Morphine may affect the properties of the blood-brain barrier (BBB) by modifying the expression of certain BBB markers. We have determined the effect of chronic morphine treatment on the expression and function of some BBB markers in the rat. The mRNAs of 19 selected genes encoding caveolins, endothelial transporters, receptors and tight junctions proteins in the total RNA of isolated cortex microvessels were assayed by quantitative RT-PCR (qRT-PCR). The expression of genes Mdr1a, Mrp1, Bcrp, Glut-1 and Occludin, was slightly increased, while that of Flk-1 was decreased in microvessels from morphine-treated rats. The expression of the Mrd1a and Mdr1b genes encoding the P-glycoprotein (P-gp) also increased in the whole hippocampus and cortex of morphine-treated rats. The Mdr1a gene induction (1.38-fold) observed by qRT-PCR was also confirmed using in situ hybridization technique (1.40-fold). Immunoblotting revealed an increase in P-gp expression in the hippocampus (1.8-fold) and cortex (1.36-fold) of morphine-treated rats, but no effect in isolated microvessels. In contrast, morphine treatment increased by 1.48-fold the expression of P-gp in a large vessel-enriched fraction. The integrity of the BBB, measured by in situ brain perfusion of [(14)C]-sucrose, and the activity of P-gp at the BBB, measured with the P-gp substrate [(3)H]-colchicine, were not modified by morphine. Immunohistofluorescence experiments revealed that P-gp expression is restricted to large vessels and microvessels in control rats and that morphine treatment did not induce the expression of P-gp in the brain parenchyma (astrocytes or neurons). Taken together, our results showed that chronic morphine treatment does not significantly alter BBB integrity or P-gp activity. The impact of morphine-mediated P-gp induction observed in large vessels remains to be determined in terms of brain disposition of drugs that are P-gp substrates.
吗啡可能通过改变某些血脑屏障(BBB)标志物的表达来影响血脑屏障的特性。我们已经确定了慢性吗啡治疗对大鼠一些血脑屏障标志物表达和功能的影响。通过定量逆转录聚合酶链反应(qRT-PCR)检测分离的皮质微血管总RNA中19个选定基因的mRNA,这些基因编码小窝蛋白、内皮转运体、受体和紧密连接蛋白。在吗啡处理大鼠的微血管中,基因Mdr1a、Mrp1、Bcrp、Glut-1和Occludin的表达略有增加,而Flk-1的表达则降低。编码P-糖蛋白(P-gp)的Mrd1a和Mdr1b基因在吗啡处理大鼠的整个海马体和皮质中的表达也增加。qRT-PCR观察到的Mdr1a基因诱导(1.38倍)也通过原位杂交技术得到证实(1.40倍)。免疫印迹显示,吗啡处理大鼠海马体(1.8倍)和皮质(1.36倍)中P-gp表达增加,但在分离的微血管中没有影响。相比之下,吗啡处理使富含大血管的部分中P-gp的表达增加了1.48倍。通过[(14)C]-蔗糖原位脑灌注测量的血脑屏障完整性,以及用P-gp底物[(3)H]-秋水仙碱测量的血脑屏障处P-gp的活性,未被吗啡改变。免疫组织荧光实验显示,在对照大鼠中,P-gp表达局限于大血管和微血管,吗啡处理并未诱导脑实质(星形胶质细胞或神经元)中P-gp的表达。综上所述,我们的结果表明,慢性吗啡治疗不会显著改变血脑屏障完整性或P-gp活性。在大血管中观察到的吗啡介导的P-gp诱导的影响,就P-gp底物药物的脑内分布而言,仍有待确定。