Said H M, Mohammadkhani R, McCloud E
Medical Research Service, Veterans Affairs Medical Center-Long Beach, CA 90822.
Proc Soc Exp Biol Med. 1993 Apr;202(4):428-34. doi: 10.3181/00379727-202-43554.
Uptake of luminal riboflavin (RF) into the absorptive cells of rabbit small intestine was examined using purified brush border membrane vesicle (BBMV) preparations. These preparations were used in order to eliminate the interference of intracellular metabolism that occurs to the RF molecule during absorption. Uptake of RF by BBMV was found to be mainly (> 76%) the result of transport of the vitamin into the intracellular space with less binding to membrane surfaces. All 3H radioactivity that appeared in the intravesicular space after incubation with [3H]RF was found to be in the form of intact RF. Uptake of RF with time was independent of the presence or absence of a Na+ or a K+ gradient (out > in) and occurred without transaccumulation of the substrate in the intravesicular space. Furthermore, changing the incubation buffer pH showed minimal effect on RF uptake. When examined as a function of concentration, the initial rate of RF uptake was found to be saturable both in jejunal and ileal BBMV with an apparent Km of 7.24 +/- 1.06 and 8.88 +/- 0.90 microM and Vmax of 24.31 +/- 1.48 and 34.24 +/- 1.55 pmol/mg protein/5 sec, respectively. Unlabeled RF and the related compounds lumiflavin, 8-aminoriboflavin, isoriboflavin, and lumichrome all inhibited (but to different degrees) the uptake of physiologic concentration of [3H]RF. On the other hand, 8-hydroxyriboflavin, lumazine, and D-ribose all failed to inhibit [3H]RF uptake. Similarly, the membrane transport inhibitors DIDS, SITS, and furosemide all failed to inhibit [3H]RF uptake. The uptake of RF was found to be insensitive to changes in the transmembrane electrical potential, as shown by studies with anion substitution and valinomycin K(+)-induced negative or positive intravesicular potential methodologies. These results indicate that RF uptake by rabbit intestinal BBMV occurs via a carrier-mediated system that is Na+ independent in nature and transports the substrate by an electroneutral process. The role of this system in the overall absorption process of RF is discussed.
利用纯化的刷状缘膜囊泡(BBMV)制剂,研究了管腔核黄素(RF)进入兔小肠吸收细胞的情况。使用这些制剂是为了消除吸收过程中RF分子发生的细胞内代谢干扰。发现BBMV对RF的摄取主要(>76%)是维生素转运到细胞内空间的结果,与膜表面的结合较少。与[3H]RF孵育后出现在囊泡内空间的所有3H放射性都以完整RF的形式存在。RF的摄取随时间变化与Na+或K+梯度(外>内)的存在与否无关,并且在囊泡内空间中不会发生底物的反积累。此外,改变孵育缓冲液的pH对RF摄取的影响最小。当作为浓度的函数进行检测时,发现空肠和回肠BBMV中RF摄取的初始速率均可饱和,其表观Km分别为7.24±1.06和8.88±0.90 microM,Vmax分别为24.31±1.48和34.24±1.55 pmol/mg蛋白质/5秒。未标记的RF以及相关化合物核黄素、8-氨基核黄素、异核黄素和核黄素均抑制(但程度不同)生理浓度[3H]RF的摄取。另一方面,8-羟基核黄素、核黄素和D-核糖均未能抑制[3H]RF的摄取。同样,膜转运抑制剂DIDS、SITS和速尿均未能抑制[3H]RF的摄取。如通过阴离子替代和缬氨霉素K(+)诱导的囊泡内负或正电位方法所进行的研究表明,RF的摄取对跨膜电位的变化不敏感。这些结果表明,兔肠道BBMV对RF的摄取是通过一种载体介导的系统进行的,该系统本质上不依赖Na+,并通过电中性过程转运底物。讨论了该系统在RF整体吸收过程中的作用。