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肉桂醛在F344大鼠中的毒代动力学

Toxicokinetics of cinnamaldehyde in F344 rats.

作者信息

Yuan J H, Dieter M P, Bucher J R, Jameson C W

机构信息

National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.

出版信息

Food Chem Toxicol. 1992 Dec;30(12):997-1004. doi: 10.1016/0278-6915(92)90109-x.

Abstract

The toxicokinetic profile of cinnamaldehyde (CNMA) was investigated in Fischer 344 rats. CNMA was found to be unstable in blood. After iv administration, a large fraction of CNMA was immediately oxidized to cinnamic acid. The biological half-life of CNMA after iv administration was found to be 1.7 hr. After administration by gavage of CNMA at 250 or 500 mg/kg body weight using corn oil as vehicle, the maximum blood concentrations of CNMA were in the order of 1 microgram/ml. These low blood concentrations were maintained over a 24-hr period after a dose of 500 mg/kg, which is relatively long considering the short (1.7 hr) biological half-life of CNMA. The estimated oral bioavailability of CNMA was less than 20% for both the 250 and 500 mg/kg doses. No CNMA was present in blood at any time in rats dosed with 50 mg CNMA/kg body weight. Only a small amount of the administered CNMA was excreted in rat urine as free cinnamic acid or beta-glucuronide-conjugated cinnamic acid. The majority of CNMA administered orally was excreted in urine as hippuric acid within 24 hr. The maximum excretion rate occurred at 8 hr after gavage. Hippuric acid recovered in 50-hr urine samples was found to be directly proportional to the oral dose of CNMA.

摘要

在Fischer 344大鼠中研究了肉桂醛(CNMA)的毒代动力学特征。发现CNMA在血液中不稳定。静脉注射后,大部分CNMA立即氧化为肉桂酸。静脉注射后CNMA的生物半衰期为1.7小时。以玉米油为载体,按250或500mg/kg体重经口灌胃给予CNMA后,CNMA的最大血药浓度约为1微克/毫升。在给予500mg/kg剂量后,这些低血药浓度在24小时内维持,考虑到CNMA较短的(1.7小时)生物半衰期,这相对较长。对于250和500mg/kg剂量,CNMA的估计口服生物利用度均小于20%。给以50mg CNMA/kg体重的大鼠在任何时候血液中均未检测到CNMA。给予的CNMA只有少量以游离肉桂酸或β-葡萄糖醛酸结合型肉桂酸的形式经大鼠尿液排泄。口服给予的大部分CNMA在24小时内以马尿酸的形式经尿液排泄。最大排泄率出现在灌胃后8小时。在50小时尿液样本中回收的马尿酸被发现与CNMA的口服剂量成正比。

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