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THE PHARMACOKINETICS OF OCHRATOXIN A IN RATS

机译:CH曲霉毒素A在大鼠体内的药代动力学

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References(33) Cited-By(31) The absorption and tissue distribution of ochratoxin A (OCT A) following a single oral dose of OCT A were investigated in adult, male Wistar rats. In experiments concerning excretory patterns of OCT A, 14C-OCT A was used. A relatively large amount of OCT A was found in the circulating blood 48 hours after dosing. The patterns of absorption, tissue distribution and excretion of OCT A were affected by acute catarrhal enteritis produced by OCT A and/or ochratoxin a (OCT α). Quantitative data show that OCT A is distributed mostly in the kidney and this finding is closely associated with the tissue specifity of OCT A-induced nephrotoxicity. OCT A was found to be hydrolyzed to its major metabolite, OCT α by addition of the homogenate of pancreas, duodenum and ileum. Approximately 56% of OCT A administered was excreted in both urine and feces as the unchanged toxin and OCT α during 120 hours following dosing. A relatively larger amount of OCT α was detected as compared with that of OCT A.
机译:参考文献(33)引用(31)研究了成年雄性Wistar大鼠单次口服OCT A后曲毒素A(OCT A)的吸收和组织分布。在有关OCTA的排泄模式的实验中,使用了14C-OCTA。给药后48小时,在循环血液中发现了相对大量的OCTA。 OCT A和/或曲霉毒素a(OCTα)产生的急性卡他性肠炎会影响OCT A的吸收,组织分布和排泄方式。定量数据表明,OCTA大部分分布在肾脏中,这一发现与OCTA诱导的肾毒性的组织特异性密切相关。通过添加胰腺,十二指肠和回肠的匀浆,发现OCT A被水解成其主要代谢产物OCTα。给药后约120%的OCT A在尿液和粪便中以未改变的毒素和OCTα的形式排泄。与OCT A相比,检测到的OCTα量相对较大。

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