Boumendil-Podevin E F, Podevin R A, Priol C
Am J Physiol. 1979 Jun;236(6):F519-25. doi: 10.1152/ajprenal.1979.236.6.F519.
The transport of uric acid was studied in brush border membrane vesicles isolated from rabbit kidney. The uptake of uric acid by the vesicles was osmotically sensitive and occurred in the absence of significant uric acid degradation. Under the conditions used to evaluate transport, urate binding to the membranes represented only 10--15% of the total uptake. The initial rate of uptake was linear over the concentration range 0.04--8 mM urate. Uptake of urage was Na+ gradient independent. It was dependent on external pH and temperature with Q10 near 3. The urate uptake was inhibited reversibly by p-chloromercuribenzoate. Probenecid, ouabain, cyclic adenosine 3',5'--monophosphate, and its dibutyryl derivative had no appreciable effects. Pyrazinoic acid and pyrazinamide stimulated urate uptake. Experiments performed with osmotically shocked vesicles demonstrated that this stimulatory effect resulted from increased binding of urate to the membranes. These results indicate that in several ways urate transport in vesicles resembles that observed with more physiologically intact preparations.
在从兔肾分离出的刷状缘膜囊泡中研究了尿酸的转运。囊泡对尿酸的摄取对渗透压敏感,且在无明显尿酸降解的情况下发生。在用于评估转运的条件下,尿酸盐与膜的结合仅占总摄取量的10%-15%。在尿酸盐浓度范围为0.04-8 mM时,摄取的初始速率呈线性。尿酸的摄取不依赖于Na+梯度。它依赖于外部pH和温度,Q10接近3。对氯汞苯甲酸可可逆地抑制尿酸盐摄取。丙磺舒、哇巴因、环腺苷3',5'-单磷酸及其二丁酰衍生物没有明显作用。吡嗪酸和吡嗪酰胺刺激尿酸盐摄取。用渗透压休克囊泡进行的实验表明,这种刺激作用是由于尿酸盐与膜的结合增加所致。这些结果表明,在几个方面,囊泡中的尿酸盐转运类似于在生理上更完整的制剂中观察到的情况。