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使用离子载体研究肾微绒毛膜囊泡中的钠离子转运途径。

Use of ionophores to study Na+ transport pathways in renal microvillus membrane vesicles.

作者信息

Aronson P S, Kinsella J L

出版信息

Fed Proc. 1981 Jun;40(8):2213-7.

PMID:6263713
Abstract

Ionophore use an illustrated by a description of experiments in which the K+ ionophore valinomycin and the uncoupler, carbonyl cyanide p-trifluoromethoxyphenylhydrazone (FCCP) were employed to investigate Na+ transport pathways in renal microvillus membrane vesicles. First, the potential-dependence of solute transport was examined by using valinomycin and K+ gradients to alter the membrane potential. Whereas Na+-glucose cotransport was voltage-sensitive, the transport of Na+ in the absence of glucose was found to occur via a voltage-insensitive process, likely Na+-H+ exchange. Second, FCCP short-circuiting of the membrane vesicles was used to examine possible electrical interactions among Na+ transport pathways. The alanine inhibition of Na+-dependent glucose transport was abolished by FCCP, indicating that the effect of the amino acid on sugar flux was indirect and mediated by an alteration in the membrane potential. Third, aspects of the molecular mechanism of Na+-glucose cotransport were evaluated by using ionophores to study the potential-dependence of phlorizin binding to the Na+-coupled sugar carrier. Whereas the rate of phlorizin association was potential-dependent, the rate of release of bound phlorizin was insensitive to variation in the transmembrane voltage, suggesting that the potential-dependence of Na+-glucose cotransport arises from potential-dependent behavior of the free carrier rather than from potential-dependence of Na+-glucose translocation per se. These studies demonstrate that the use of ionophores augments the value of employing isolated plasma membrane vesicles to investigate mechanisms of epithelial solute transport.

摘要

离子载体的应用通过实验描述得以说明,在这些实验中,钾离子载体缬氨霉素和解偶联剂羰基氰对三氟甲氧基苯腙(FCCP)被用于研究肾微绒毛膜囊泡中的钠离子转运途径。首先,通过使用缬氨霉素和钾离子梯度来改变膜电位,研究了溶质转运的电位依赖性。虽然钠-葡萄糖共转运对电压敏感,但发现在无葡萄糖情况下钠离子的转运是通过一种电压不敏感的过程进行的,可能是钠-氢交换。其次,利用FCCP使膜囊泡短路来研究钠离子转运途径之间可能存在的电相互作用。FCCP消除了丙氨酸对钠依赖性葡萄糖转运的抑制作用,这表明氨基酸对糖通量的影响是间接的,并且是由膜电位的改变介导的。第三,通过使用离子载体研究根皮苷与钠偶联糖载体结合的电位依赖性,评估了钠-葡萄糖共转运分子机制的各个方面。虽然根皮苷结合速率对电位有依赖性,但结合的根皮苷释放速率对跨膜电压的变化不敏感,这表明钠-葡萄糖共转运的电位依赖性源于游离载体的电位依赖性行为,而不是钠-葡萄糖转运本身的电位依赖性。这些研究表明,离子载体的使用提高了利用分离的质膜囊泡研究上皮溶质转运机制的价值。

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