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外排转运体抑制对氟康唑在大鼠脑内分布的影响。

Effect of Efflux Transporter Inhibition on the Distribution of Fluconazole in the Rat Brain.

作者信息

Wang Wei, Zheng Na, Zhang Jiatang, Huang Xusheng, Yu Shengyuan

机构信息

Department of Neurology, General Hospital of People's Liberation Army, No. 28, Fuxing Road, Haidian District, Beijing, 100853, China.

出版信息

Neurochem Res. 2017 Aug;42(8):2274-2281. doi: 10.1007/s11064-017-2240-x. Epub 2017 Mar 24.

Abstract

Multidrug resistance-associated proteins (MRPs) and organic anion transporters (OATs) are expressed on the blood-brain barrier (BBB) and blood-cerebrospinal fluid barrier (BCSFB), preventing the entry of or the pumping out of numerous molecules. Fluconazole is widely used to treat fungal meningoencephalitis. The effect of these transporters on the distribution of fluconazole in the brain is unclear. We used microdialysis to compare the distribution of fluconazole in the rat brain with and without co-administration of probenecid, a MRP and OAT inhibitor. Additionally, we also observed the difference in fluconazole distribution between the two barriers. The results showed that probenecid increased the penetration of fluconazole into the BBB but did not alter the penetration of fluconazole into the BCSFB of rats. The penetration of the BBB and BCSFB by fluconazole did not statistically differ according to physiological condition. These results demonstrate that transporters that can be inhibited by probenecid may be involved in fluconazole resistance at the BBB and provide a laboratory basis for predicting brain extracellular fluid (ECF) concentration using the cerebrospinal fluid (CSF) concentration of fluconazole.

摘要

多药耐药相关蛋白(MRPs)和有机阴离子转运体(OATs)在血脑屏障(BBB)和血脑脊液屏障(BCSFB)上表达,可阻止众多分子的进入或泵出。氟康唑广泛用于治疗真菌性脑膜脑炎。这些转运体对氟康唑在脑内分布的影响尚不清楚。我们使用微透析技术比较了在联合使用丙磺舒(一种MRP和OAT抑制剂)与未使用丙磺舒的情况下,氟康唑在大鼠脑内的分布情况。此外,我们还观察了氟康唑在两种屏障之间分布的差异。结果显示,丙磺舒增加了氟康唑对血脑屏障的穿透,但并未改变氟康唑对大鼠血脑脊液屏障的穿透。根据生理状态,氟康唑对血脑屏障和血脑脊液屏障的穿透在统计学上并无差异。这些结果表明,可被丙磺舒抑制的转运体可能与血脑屏障处的氟康唑耐药有关,并为利用氟康唑的脑脊液(CSF)浓度预测脑细胞外液(ECF)浓度提供了实验室依据。

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