Suppr超能文献

黄曲霉毒素 A 在 F344 大鼠中的代谢和毒代动力学。

Metabolism and toxicokinetics of the mycotoxin ochratoxin A in F344 rats.

机构信息

Institut für Toxikologie, Universität Würzburg, Versbacher Str. 9, 97078, Würzburg, Germany.

出版信息

Mycotoxin Res. 2003 Jun;19(2):102-7. doi: 10.1007/BF02942946.

Abstract

Male (n=18) and female (n=18) F344 rats were administered a single dose of OTA (0.5 mg/kg b.w.) in corn oil by gavage. Animals (n=3) were sacrificed 24, 48, 72, 96, 672 and 1,344 hours after OTA administration and concentrations of OTA and OTA-metabolites in urine, feces, blood, liver and kidney were determined by HPLC with fluorescence detection and/or by LC-MS/MS. Recovery of unchanged OTA in urine amounted to 2.1% of dose in males and 5.2% in females within 96 h. In feces, only 5.5% resp. 1.5% of dose were recovered. The major metabolite detected was OTalpha, low concentrations of OTA-glucosides were also present in urine. Other postulated metabolites were not observed. The maximal blood levels of OTA were observed between 24 and 48h after administration and were app. 4.6 µmol/l in males and 6.0 µmol/l in females. Elimination of OTA from blood followed first-order kinetics with a half-life of app. 230h calculated from 48h to 1344h. In liver of both male and female rats OTA-concentrations were less than 12 pmol/g tissue, with a maximum at 24h after administration. In contrast, OTA accumulated in the kidneys, reaching a concentration of 480 pmol/g tissue in males 24h after OTA-administration. In general, tissue concentrations in males were higher than in females. OTalpha was not detected in liver and kidney tissue of rats administered OTA and OTalpha concentrations in blood were low (10-15 nmol/1). The high concentrations of OTA in kidneys of male rats may explain the organ- and gender-specific toxicity of OTA.

摘要

雄性(n=18)和雌性(n=18)F344 大鼠经灌胃给予玉米油中的单剂量 OTA(0.5mg/kg bw)。动物(n=3)在 OTA 给药后 24、48、72、96、672 和 1344 小时被处死,并用 HPLC 荧光检测和/或 LC-MS/MS 测定尿液、粪便、血液、肝脏和肾脏中的 OTA 和 OTA 代谢物浓度。在 96 小时内,雄性尿中未改变的 OTA 回收率为剂量的 2.1%,雌性为 5.2%。粪便中,仅回收了剂量的 5.5%和 1.5%。检测到的主要代谢物是 OTalpha,尿液中也存在低浓度的 OTA-葡糖苷。未观察到其他假定的代谢物。给药后 24 至 48 小时观察到 OTA 的最大血液水平,雄性约为 4.6µmol/l,雌性约为 6.0µmol/l。从 48 小时到 1344 小时,OTa 从血液中的消除遵循一级动力学,半衰期约为 230 小时。在雄性和雌性大鼠的肝脏中,OTA 浓度均小于 12pmol/g 组织,给药后 24 小时达到最大值。相比之下,OTA 在肾脏中积累,雄性大鼠在给药后 24 小时达到 480pmol/g 组织的浓度。一般来说,雄性组织中的浓度高于雌性。给予 OTA 的大鼠的肝和肾组织中未检测到 OTalpha,血液中的 OTalpha 浓度较低(10-15nmol/1)。雄性大鼠肾脏中 OTA 的高浓度可能解释了 OTA 的器官和性别特异性毒性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验