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棉酚在兔体内的肾脏转运

Renal transport of gossypol in the rabbit.

作者信息

Goldinger J M, Lee S H, Hong S K

出版信息

Proc Soc Exp Biol Med. 1985 May;179(1):50-4. doi: 10.3181/00379727-179-42063.

Abstract

The present work was carried out to investigate the transport characteristics of gossypol, a toxic weak organic acid (pK = 7.2) contained in cottonseed, into the rabbit renal cortical slice. The uptake of gossypol increased linearly during a 2-hr incubation after which it leveled off with the average slice-to-medium concentration ratio (S/M) slightly above 20. In the presence of metabolic inhibitors, the S/M gossypol leveled off at about 9, suggesting an extensive binding of gossypol to tissue proteins. The uptake of gossypol was significantly inhibited by p-aminohippurate (PAH), probenecid, ouabain, and DIDS, all of which are known inhibitors of renal organic anion transport. However, the gossypol uptake was not affected by tetraethylammonium (TEA), a prototypical organic cation. Kinetic studies indicated that the apparent Km for gossypol transport is 0.28 mM, and also that probenecid inhibits gossypol transport in a competitive manner. It is concluded that gossypol is transported by the renal tubule through the classic organic anion system.

摘要

开展本研究旨在探究棉籽中含有的有毒弱酸(pK = 7.2)棉酚进入兔肾皮质切片的转运特性。在2小时的孵育过程中,棉酚的摄取呈线性增加,之后趋于平稳,切片与介质的平均浓度比(S/M)略高于20。在存在代谢抑制剂的情况下,棉酚的S/M水平稳定在约9,这表明棉酚与组织蛋白存在广泛结合。对氨基马尿酸(PAH)、丙磺舒、哇巴因和二异丙基氟磷酸(DIDS)均显著抑制棉酚的摄取,所有这些都是已知的肾有机阴离子转运抑制剂。然而,棉酚的摄取不受典型有机阳离子四乙铵(TEA)的影响。动力学研究表明,棉酚转运的表观Km为0.28 mM,丙磺舒也以竞争性方式抑制棉酚转运。得出的结论是,棉酚通过肾小管经经典有机阴离子系统进行转运。

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