A 90-Day Repeated Oral Dose Toxicity Study of Alismatis Rhizoma Aqueous Extract in Rats

被引:14
|
作者
Lee, Mu-Jin [1 ,2 ]
Jung, Ho-Kyung [1 ]
Lee, Ki-Ho [1 ]
Jang, Ji-Hun [1 ]
Sim, Mi-Ok [1 ]
Seong, Tea-Gyeong [1 ]
Ahn, Byung-Kwan [1 ]
Shon, Jin-Han [1 ]
Ham, Seong-Ho [1 ]
Cho, Hyun-Woo [1 ]
Kim, Yong-Min [3 ]
Park, Sung-Jin [3 ]
Yoon, Ji-Young [4 ]
Ko, Je-Won [2 ]
Kim, Jong-Choon [2 ]
机构
[1] Natl Dev Inst Korean Med, Div Tradit Korean Med Res, 288 Udeuraendeu Gil, Jangheung 59338, Jeonnam, South Korea
[2] Chonnam Natl Univ, Coll Vet Med, BK21 Plus Project Team, 77 Yongbong Ro, Gwangju 61186, South Korea
[3] MEDVILL Co, Preclin Res Ctr, Seoul, South Korea
[4] Jeonju AgroBiomat Inst, Jeonju, South Korea
基金
新加坡国家研究基金会;
关键词
Alismatis rhizome aqueous extract; Traditional medicine; Diuretic effect; Sub-chronic toxicity; NOAEL; CHRONIC PROGRESSIVE NEPHROPATHY; TRITERPENE; ORIENTALE;
D O I
10.5487/TR.2019.35.2.191
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Alismatis rhizoma (AR), the dried rhizome of Alisma orientale (Sam.) Juzep, is a well-known, traditional medicine that is used for the various biological activities including as a diuretic, to lower cholesterol and as an anti-inflammatory agent. The present study was carried out to investigate the potential toxicity of the Alismatis rhizoma aqueous extract (ARAE) following 90-day repeated oral administration to Sprague-Dawley rats. ARAE was administered orally to male and female rats for 90 days at 0 (control), 500, 1,000 and 2,000 mg/kg/day (n =10 for male and female rats for each dose). Additional recovery groups from the control group and high dose group were observed for a 28-day recovery period. Chromatograms of ARAE detected main compounds with four peaks. Treatment-related effects including an increase in the red blood cells, hemoglobin, hematocrit, albumin, total protein, and urine volume were observed in males of the 2,000 mg/kg/day group (p < 0.05). However, the diuretic effect of ARAE was considered, a major cause of hematological and serum biochemical changes. The oral no-observed-adverse-effect level (NOAEL) of the ARAE was > 2,000 mg/kg/day in both genders, and no target organs were identified.
引用
收藏
页码:191 / 200
页数:10
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