Chatton J Y, Odone M, Besseghir K, Roch-Ramel F
Institut de Pharmacologie de l'Université, Lausanne, Switzerland.
J Pharmacol Exp Ther. 1990 Oct;255(1):140-5.
The renal excretion of 3'-azido-3'-deoxythymidine (AZT) was investigated in clearance experiments in anesthetized rats. AZT was filtered freely and subsequently secreted, reabsorption being of minor importance. Probenecid, the classical inhibitor organic anion secretion, decreased AZT secretion. AZT, on the other hand, decreased p-aminohippurate secretion. These observations demonstrate that AZT is secreted by the organic anion secretory mechanisms. Cimetidine, an organic cation, also decreased AZT secretion at a concentration which did not inhibit the secretion of the organic anion, p-aminohippurate. This suggests that AZT might also be transported by the mechanisms secreting organic cations. However, as AZT did not inhibit the secretion of the organic cation tetraethylammonium, it cannot be concluded that AZT is transported by the mechanisms secreting organic cations.
在麻醉大鼠的清除实验中研究了3'-叠氮-3'-脱氧胸苷(AZT)的肾脏排泄。AZT可自由滤过,随后被分泌,重吸收作用较小。丙磺舒,经典的有机阴离子分泌抑制剂,可减少AZT的分泌。另一方面,AZT可减少对氨基马尿酸盐的分泌。这些观察结果表明AZT是通过有机阴离子分泌机制进行分泌的。西咪替丁,一种有机阳离子,在不抑制有机阴离子对氨基马尿酸盐分泌的浓度下,也可减少AZT的分泌。这表明AZT也可能通过分泌有机阳离子的机制进行转运。然而,由于AZT不抑制有机阳离子四乙铵的分泌,因此不能得出AZT是通过分泌有机阳离子的机制进行转运的结论。