Acute toxicity of berberine and its correlation with the blood concentration in mice

被引:239
作者
Kheir, Michael M. [1 ,2 ,3 ]
Wang, Yugang [1 ]
Hua, Lei [1 ]
Hu, Jun [1 ]
Li, Lele [1 ]
Lei, Fan [1 ]
Dua, Lijun [1 ]
机构
[1] Tsinghua Univ, Lab Pharmaceut Sci, Sch Life Sci, Beijing 100084, Peoples R China
[2] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Psychol, Ann Arbor, MI 48109 USA
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
Berberine; Acute toxicity; HPLC; Pharmacokinetics; Mice; IN-VITRO; MECHANISM; EFFICACY; PLASMA;
D O I
10.1016/j.fct.2010.01.033
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
The aim of this study was to investigate the LD50 (median lethal dosage) of berberine (BBR) through three different routes of injection in mice: intravenous (IV) injection, intraperitoneal (IP) injection, and intragastric (IG) oral administration. The concentration of BBR in blood from their IG doses (10.4, 20.8, 41.6, and 83.2 g/kg) and the content relationship of BBR among different injections were analyzed by high-performance liquid chromatography (HPLC). The LD50 of BBR from IV and IP injections is 9.0386 and 57.6103 mg/kg, respectively; but no LD50 was found in the IG group. A significant difference in bioavailability was observed between the different routes. Furthermore, the concentration of BBR in the blood from different IG doses was also significantly different. However, we discovered an interesting phenomenon indicating that the absorption of BBR by oral administration has a limit, therefore, explaining the difficulty in obtaining an LD50 of BBR for IG injection. From the analysis of BBR content in blood after various administrations, we hypothesized that not only does the concentration of BBR in blood contribute to its acute toxicity, but also the routes of administration may be an important facet that affects this toxicity evaluation. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1105 / 1110
页数:6
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