Proctor William R, Ming Xin, Bourdet David, Han Tianxiang Kevin, Everett Ruth S, Thakker Dhiren R
Division of Molecular Pharmaceutics, UNC Eshelman School of Pharmacy, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599.
Division of Pharmacotherapy and Experimental Therapeutics, UNC Eshelman School of Pharmacy, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599.
J Pharm Sci. 2016 Feb;105(2):484-496. doi: 10.1016/j.xphs.2015.11.040.
Transport proteins in intestinal epithelial cells facilitate absorption of nutrients/compounds that are organic anions, cations, and zwitterions. For two decades, we have studied intestinal absorption and transport of hydrophilic ionic compounds, with specific focus on transport properties of organic cations and their interactions with intestinal transporters and tight junction proteins. Our data reveal how complex interactions between a compound and transporters in intestinal apical/basolateral (BL) membranes and tight junction proteins define oral absorption, and that the BL membrane lacks an efflux transporter that can transport positively charged compounds. Based on our investigations of transport mechanisms of zwitterionic, anionic, and cationic compounds, we postulate that physicochemical properties of these ionic species, in relation to the intestinal micro pH environment, have exerted evolutionary pressure for development of transporters that can handle apical uptake/efflux of all 3 ionic species and BL efflux of anions and zwitterions, but such evolutionary pressure is lacking for development of a BL efflux transporter for cationic compounds. This review provides an overview of intestinal uptake/efflux transporters and describes our studies on intestinal transport of cationic, anionic, and zwitterionic drugs that led to hypothesize that there are no cation-selective BL efflux transporters in the intestine.
肠上皮细胞中的转运蛋白有助于吸收有机阴离子、阳离子和两性离子等营养物质/化合物。二十年来,我们一直在研究亲水性离子化合物的肠道吸收和转运,特别关注有机阳离子的转运特性及其与肠道转运体和紧密连接蛋白的相互作用。我们的数据揭示了化合物与肠道顶端/基底外侧(BL)膜中的转运体以及紧密连接蛋白之间复杂的相互作用如何决定口服吸收,并且BL膜缺乏能够转运带正电荷化合物的外排转运体。基于我们对两性离子、阴离子和阳离子化合物转运机制的研究,我们推测这些离子物种的物理化学性质,相对于肠道微pH环境,对能够处理所有三种离子物种的顶端摄取/外排以及阴离子和两性离子的BL外排的转运体的发育施加了进化压力,但对于阳离子化合物的BL外排转运体的发育缺乏这种进化压力。本综述概述了肠道摄取/外排转运体,并描述了我们对阳离子、阴离子和两性离子药物肠道转运的研究,这些研究导致我们假设肠道中不存在阳离子选择性BL外排转运体。