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藤黄酸及其在实验动物中的潜在靶点的毒理学研究。

Toxicological studies of gambogic acid and its potential targets in experimental animals.

作者信息

Guo Qinglong, Qi Qi, You Qidong, Gu Hongyan, Zhao Li, Wu Zhaoqiu

机构信息

Department of Physiology, China Pharmaceutical University, 24 Tongjian Xiang, Nanjing 210009, China.

出版信息

Basic Clin Pharmacol Toxicol. 2006 Aug;99(2):178-84. doi: 10.1111/j.1742-7843.2006.pto_485.x.

Abstract

Acute and chronic toxicity of gambogic acid, a promising novel anticancer agent, was determined using albino mice and Beagle dogs as model animals. Histopathological examination and viscera parameter investigation were also carried out after autopsy. The LD50 of gambogic acid was found to be 45 approximately 96 mg/kg and the 95% confidence limit was determined to be 43.18 approximately 48.45 mg/kg. The results from the chronic toxicity studies demonstrated that the toxicity targets in the experimental animals were liver and kidney. The innocuous dose was established to be 4 mg/kg after administration to dogs for a total of 13 weeks at a frequency of one injection every other day. This dose (4 mg/kg) was approximately 9.6 (body weight) or 5.1 (body surface area) times the dosage (25 mg/60 kg, every other day) recommended for human trials. Our results provide the theoretical foundation for clinical applications of this promising natural anticancer agent and will likely bring about considerable economic and social benefits.

摘要

以白化小鼠和比格犬作为模式动物,测定了有望成为新型抗癌剂的藤黄酸的急性和慢性毒性。尸检后还进行了组织病理学检查和内脏参数研究。藤黄酸的半数致死量(LD50)约为45至96毫克/千克,95%置信限确定为43.18至48.45毫克/千克。慢性毒性研究结果表明,实验动物的毒性靶器官是肝脏和肾脏。在以隔日注射一次的频率给犬给药共13周后,确定无害剂量为4毫克/千克。该剂量(4毫克/千克)约为人类试验推荐剂量(25毫克/60千克,隔日一次)的9.6倍(体重)或5.1倍(体表面积)。我们的研究结果为这种有前景的天然抗癌剂的临床应用提供了理论基础,并可能带来可观的经济和社会效益。

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