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丙磺舒代谢物脑脊液浓度及生物活性的定量分析。

Quantitation of CSF concentrations and biological activity of probenecid metabolites.

作者信息

Roos B E, Wickström G, Hartvig P, Nilsson J L

出版信息

Eur J Clin Pharmacol. 1980;17(3):223-6. doi: 10.1007/BF00561904.

Abstract

The concentrations of probenecid and four of its metabolites have been examined in plasma and CSF by electron capture gas chromatography after extractive methylation. The plasma concentration of each of the metabolites was in the range 1,5-15 micrograms/ml and constituted less than 10% of the parent compound. The penetration into CSF of the metabolites was lower than that of probenecid. The concentration of each of the metabolites was below 0,2 microgram/ml and the total concentration never exceeded 10% of the probenecid concentration. The inhibitory effect of the metabolites on uptake was tested in rabbit renal cortex using 3H-p-amino-hippuric acid. The inhibitory effect was low. From the low activity and relatively low concentrations of the metabolites do not contribute to the probenecid-induced blocking effect of acid transport from the CSF.

摘要

经萃取甲基化后,采用电子捕获气相色谱法检测了丙磺舒及其四种代谢物在血浆和脑脊液中的浓度。每种代谢物的血浆浓度在1.5 - 15微克/毫升范围内,占母体化合物的比例不到10%。代谢物进入脑脊液的渗透率低于丙磺舒。每种代谢物的浓度均低于0.2微克/毫升,总浓度从未超过丙磺舒浓度的10%。在兔肾皮质中使用3H - 对氨基马尿酸测试了代谢物对摄取的抑制作用。抑制作用较低。由于代谢物活性低且浓度相对较低,它们对丙磺舒诱导的脑脊液酸转运阻断作用没有贡献。

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