Tega Yuma, Yamazaki Yuhei, Akanuma Shin-Ichi, Kubo Yoshiyuki, Hosoya Ken-Ichi
Department of Pharmaceutics, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama.
Biol Pharm Bull. 2018;41(9):1330-1336. doi: 10.1248/bpb.b18-00134.
Nicotine, an addictive substance, is absorbed from the lungs following inhalation of tobacco smoke, and distributed to various tissues such as liver, brain, and retina. Recent in vivo and in vitro studies suggest the involvement of a carrier-mediated transport process in nicotine transport in the lung, liver, and inner blood-retinal barrier. In addition, in vivo studies of influx and efflux transport of nicotine across the blood-brain barrier (BBB) revealed that blood-to-brain influx transport of nicotine is more dominant than brain-to-blood efflux transport of nicotine. Uptake studies in TR-BBB13 cells, which are an in vitro model cell line of the BBB, suggest the involvement of H/organic cation antiporter, which is distinct from typical organic cation transporters, in nicotine transport at the BBB. Moreover, inhibition studies in TR-BBB13 cells showed that nicotine uptake was significantly reduced by central nervous system (CNS) drugs, such as antidepressants, anti-Alzheimer's disease drugs, and anti-Parkinson's disease drugs, suggesting that the nicotine transport system can recognize these molecules. The cumulative evidence would be helpful to improve our understanding of smoking-CNS drug interaction for providing appropriate medication.
尼古丁是一种成瘾性物质,吸入烟草烟雾后会从肺部吸收,并分布到肝脏、大脑和视网膜等各种组织中。最近的体内和体外研究表明,载体介导的转运过程参与了尼古丁在肺、肝脏和血视网膜内屏障中的转运。此外,尼古丁跨血脑屏障(BBB)的流入和流出转运的体内研究表明,尼古丁从血液到大脑的流入转运比尼古丁从大脑到血液的流出转运更为显著。在TR-BBB13细胞(一种血脑屏障的体外模型细胞系)中的摄取研究表明,与典型有机阳离子转运体不同的H/有机阳离子反向转运体参与了血脑屏障处的尼古丁转运。此外,TR-BBB13细胞中的抑制研究表明,抗抑郁药、抗阿尔茨海默病药物和抗帕金森病药物等中枢神经系统(CNS)药物可显著降低尼古丁摄取,这表明尼古丁转运系统能够识别这些分子。这些累积证据将有助于增进我们对吸烟与中枢神经系统药物相互作用的理解,从而提供适当的药物治疗。