Evaluation of acute and subacute toxicity of sodium taurodeoxycholate in rats

被引:16
作者
Choi, Hyung Jun [1 ,2 ]
Yun, Jun-Won [3 ]
Kim, Youn-Hee [4 ]
Kwon, Euna [2 ]
Hyon, Min-Kyong [1 ,2 ]
Kim, Ji Young [1 ,2 ]
Che, Jeong-Hwan [5 ]
Kim, Woo Ho [6 ]
Seong, Seung-Yong [4 ]
Kang, Byeong-Cheol [1 ,2 ,5 ,7 ]
机构
[1] Seoul Natl Univ, Coll Med, Grad Sch Translat Med, 103 Daehak Ro, Seoul 03080, South Korea
[2] Seoul Natl Univ Hosp, Biomed Res Inst, Dept Expt Anim Res, Seoul, South Korea
[3] Catholic Univ Korea, Dept Biotechnol, Bucheon, South Korea
[4] Seoul Natl Univ, Wide River Inst Immunol, Dept Microbiol & Immunol, Dept Biomed Sci,Coll Med, 103 Daehak Ro, Seoul 03080, South Korea
[5] Seoul Natl Univ, Biomed Ctr Anim Resource & Dev, Coll Med, Seoul, South Korea
[6] Seoul Natl Univ, Dept Pathol, Coll Med, Seoul, South Korea
[7] Seoul Natl Univ, Inst GreenBio Sci Technol, gDesigned Anim & Transplantat Res Inst, Gangwon, South Korea
基金
新加坡国家研究基金会;
关键词
Taurodeoxycholate; acute toxicity; subacute toxicity; bile acid; sepsis; SALT-DEPENDENT LIPASE; BILE-ACIDS; TAUROHYODEOXYCHOLIC ACID; ASPIRIN; PREVENTION; RECEPTORS; SECRETION;
D O I
10.1080/01480545.2019.1609493
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Taurodeoxycholate (TDCA) inhibits various inflammatory responses suggesting potential clinical application. However, the toxicity of TDCA has not been evaluated in detail in vivo. We investigated the acute toxicity and 4-week repeated-dose toxicity of TDCA following intravenous infusion under Good Laboratory Practice regulations. In the sighting study of acute toxicity, one of two rats (one male and one female) treated with 300 mg/kg TDCA died with hepatotoxicity, suggesting that the approximate 50% lethal dose of TDCA is 300 mg/kg. Edema and discoloration were observed at the injection sites of tails when rats were infused with 150 mg/kg or higher amount of TDCA once. In 4-week repeated-dose toxicity study, no treatment-related mortality or systemic changes in hematology and serum biochemistry, organ weights, gross pathology, or histopathology were observed. However, the tail injection site showed redness, discharge, hardening, and crust formation along with histopathological changes such as ulceration, edema, fibrosis, and thrombosis when rats were infused with 20 mg/kg TDCA. Taken together, TDCA induced no systemic toxicity or macroscopic lesions at the injection site at a dose of 10 mg/kg/day, which is 33 times higher than the median effective dose observed in a mouse sepsis model. These findings suggest that TDCA might have a favorable therapeutic index in clinical applications.
引用
收藏
页码:268 / 276
页数:9
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