A subchronic toxicity study of Radix Dipsaci water extract by oral administration in F344 rats

被引:15
|
作者
Han, Ji-Seok [1 ]
Lee, Byoung-Seok [1 ]
Han, So-Ri [2 ]
Han, Hyoung-Yun [2 ]
Chung, Moon-Koo [2 ]
Min, Byung-Sun [3 ]
Seok, Ji Hyeon [4 ]
Kim, Yong-Bum [1 ]
机构
[1] Korea Inst Toxicol, Res Ctr Toxicol Pathol, 141 Gajeong Ro, Daejeon 305343, South Korea
[2] Korea Inst Toxicol, Res Ctr Gen & Appl Toxicol, 141 Gajeong Ro, Daejeon 305343, South Korea
[3] Catholic Univ Daegu, Coll Pharm, 13-13 Hayang Ro, Gyongsan 712702, Gyeongsangbuk D, South Korea
[4] Natl Inst Food & Drug Safety Evaluat, Toxicol Evaluat & Res Dept, Toxicol Res Div, Osong Hlth Technol Adm Complex, Cheongju 363951, Chungcheongbuk, South Korea
关键词
Radix Dipsaci; Subchronic toxicity; Traditional medicines; IRIDOID GLUCOSIDE; MEDICINE; SAPONINS; LOGANIN; ROOTS; BONE;
D O I
10.1016/j.yrtph.2016.07.017
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Radix Dipsaci, the dried root of Dipsacus asperoides C.Y. Cheng & T.M.Ai, has therapeutic effects on various disorders, and in particular, bone and joint disease. Despite such ethnomedicinal benefits, there is very little information regarding its in vivo toxicity or adverse effects. This study was conducted to evaluate the potential toxicity of the Radix Dipsaci water Extract (RD-wE) by using F344 rats. The RD-wE was administered orally to rats at doses of 0, 125, 250, 500,1000, and 2000 mg/kg body weight (bw)/day for 13 weeks. During the treatment period there were no mortalities attributed to RD-wE. Moreover, no toxic effects were observed with regard to body weight, clinical pathology (hematology, clinical biochemistry, and urinalysis), and anatomic pathology (gross findings, organ weight, and microscopic examination). The changes related to the treatment were excessive salivation at the mouth and soft feces, observed in male and female rats at 1000 or 2000 mg/kg bw/day, but these were not accompanied by any microscopic correlate or other pathophysiological changes. Based on these results, the oral no-observed adverse-effect level of the RD-wE was considered to be 2000 mg/kg bw/day in both genders, although the target organs were not determined under the current experimental conditions. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:136 / 145
页数:10
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