Murakami Hideyasu, Ohkura Airi, Takanaga Hitomi, Matsuo Hirotami, Koyabu Noriko, Naito Mikihiko, Tsuruo Takashi, Ohtani Hisakazu, Sawada Yasufumi
Department of Medico-Pharmaceutical Sciences, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Int J Pharm. 2005 Feb 16;290(1-2):37-44. doi: 10.1016/j.ijpharm.2004.11.005. Epub 2005 Jan 4.
We investigated transport characteristics of adenosine across the blood-brain barrier (BBB) in mice. Uptake clearance across the BBB was measured by using an in situ mouse brain perfusion technique and cultured mouse brain capillary endothelial cell line (MBEC4 cells). Nucleoside transporter was cloned by RT-PCR and expressed on Xenopus laevis oocyte. Both in situ and in vitro studies revealed that the adenosine uptake is concentration-dependent, Na(+)-independent and S-(p-nitrobenzyl)-6-thioinosine (NBMPR)-sensitive. The K(t) values of in situ and in vitro studies were 31.7 +/- 13.8 microM and 11.9 +/- 2.84 microM, respectively. A good correlation was found for the inhibitory effects of nucleoside analogs to adenosine uptake between in situ and in vitro studies. RT-PCR revealed the expression of RNA of mouse equilibrative nucleoside transporter (mENT1) in mouse brain capillary and MBEC4 cells. In mENT1 expressed on X. laevis oocyte, K(t) value of adenosine transport was 6.9 +/- 2.7 microM (and comparable to those in situ and in vitro studies). In conclusion, we characterized the adenosine transport across the BBB in mice by using in situ brain perfusion technique and MBEC4 cells and found that these transports share common characteristics with mENT1-mediated transport. Transport of adenosine across the BBB in mice may be attributable to mENT1.
我们研究了小鼠体内腺苷通过血脑屏障(BBB)的转运特性。采用原位小鼠脑灌注技术和培养的小鼠脑微血管内皮细胞系(MBEC4细胞)测量腺苷通过血脑屏障的摄取清除率。通过逆转录聚合酶链反应(RT-PCR)克隆核苷转运体,并将其在非洲爪蟾卵母细胞上表达。原位和体外研究均表明,腺苷摄取呈浓度依赖性、不依赖钠离子且对S-(对硝基苄基)-6-硫代肌苷(NBMPR)敏感。原位和体外研究的K(t)值分别为31.7±13.8微摩尔和11.9±2.84微摩尔。原位和体外研究中核苷类似物对腺苷摄取的抑制作用之间存在良好的相关性。RT-PCR显示小鼠脑微血管和MBEC4细胞中存在小鼠平衡核苷转运体(mENT1)的RNA表达。在非洲爪蟾卵母细胞上表达的mENT1中,腺苷转运的K(t)值为6.9±2.7微摩尔(与原位和体外研究结果相当)。总之,我们利用原位脑灌注技术和MBEC4细胞对小鼠体内腺苷通过血脑屏障的转运进行了表征,发现这些转运与mENT1介导的转运具有共同特征。小鼠体内腺苷通过血脑屏障的转运可能归因于mENT1。