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恒河猴和犬中氨甲蝶呤的肾小管转运

Renal tubular transport of methotrexate in the rhesus monkey and dog.

作者信息

Huang K C, Wenczak B A, Liu Y K

出版信息

Cancer Res. 1979 Dec;39(12):4843-8.

PMID:115582
Abstract

The mechanism and localization of renal transport of methotrexate (MTX) were studied in the rhesus monkey and the dog. It was found that in both animals MTX was bound with plasma protein in a range of 50 to 68% varying with the MTX plasma concentration. Paper chromatographic analysis showed that a negligible amount of MTX was metabolized. The excretion of MTX in rhesus monkey was mainly by tubular secretion which was blocked by probenecid, but in the dog a bidirectional transport mechanism for MTX was indicated. Tubular secretion was localized in the proximal tubules, and a tubular reabsorptive process was in the distal section. Simultaneous administration of folic acid blocked the tubular reabsorption of MTX, resulting in an increase of renal excretion. Maximum tubular excretory capacity determination showed that a maximum tubular excretory capacity value of approximately 5 mumol/100 ml of glomerular filtrate was observed in the rhesus monkey at a plasma concentration of 0.07 mM and a value of 2 mumol/100 ml of glomerular filtrate for the dog. Studies with renal cortical slice technique also indicated that the monkey kidney can accumulate greater amounts of MTX than can the dog kidney.

摘要

在恒河猴和狗身上研究了甲氨蝶呤(MTX)的肾脏转运机制及定位。发现两种动物体内的MTX与血浆蛋白结合率在50%至68%之间,随血浆MTX浓度而变化。纸色谱分析表明,MTX代谢量可忽略不计。恒河猴体内MTX的排泄主要通过肾小管分泌,丙磺舒可阻断该过程,但在狗体内,MTX显示出双向转运机制。肾小管分泌定位于近端小管,而肾小管重吸收过程发生在远端部分。同时给予叶酸可阻断MTX的肾小管重吸收,导致肾脏排泄增加。最大肾小管排泄能力测定表明,恒河猴在血浆浓度为0.07 mM时,最大肾小管排泄能力值约为5 μmol/100 ml肾小球滤液,狗的该值为2 μmol/100 ml肾小球滤液。肾皮质切片技术研究还表明,猴肾比狗肾能积累更多的MTX。

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