Acute and Chronic Toxicity of Indole Alkaloids from Leaves of Alstonia scholaris (L.) R. Br. in Mice and Rats

被引:28
作者
Zhao, Yun-Li [1 ,3 ]
Su, Min [2 ]
Shang, Jian-Hua [2 ,3 ]
Wang, Xia [2 ]
Njateng, Guy Sedar Singor [4 ]
Bao, Guang-Lei [2 ]
Ma, Jia [2 ]
Sun, Qing-Di [5 ]
Yuan, Fang [2 ]
Wang, Jing-Kun [2 ]
Luo, Xiao-Dong [1 ,3 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China
[2] Yunnan Inst Med Mat, Kunming 650111, Yunnan, Peoples R China
[3] Yunnan Univ, Sch Chem Sci & Technol, Key Lab Med Chem Nat Resource, Minist Educ & Yunnan Prov, Kunming 650091, Yunnan, Peoples R China
[4] Univ Dschang, Fac Sci, Lab Microbiol & Antimicrobial Subst, POB 67, Dschang, Cameroon
[5] Jiangsu Nhwa Pharmaceut Co Ltd, Xuzhou 221009, Jiangsu, Peoples R China
关键词
Alstonia scholaris; Indole alkaloids; Acute toxicity; Chronic toxicity; Non-observed-adverse-effect-level; FLIGHT MASS-SPECTROMETRY; EXTRACT; IDENTIFICATION; CONSTITUENTS; SAFETY;
D O I
10.1007/s13659-020-00237-1
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Alstonia scholaris (L.) R. Br. (Apocynaceae) is an evergreen tree that has been used to treat lung diseases. In this study, the toxicity profile of indole alkaloids from leaves of A. scholaris was investigated. In acute toxicity tests, mice were administered total alkaloids (TA) and five indole alkaloids. In a chronic toxicity test, rats were continuously administered TA (50, 100, and 300 mg/kg bw) for 13 weeks, followed by a 4-week recovery. A single administration of TA affected the behavior of mice, and at 12.8 g/kg bw, prone position, shortness of breath, wheezing, and convulsion were observed. The half-lethal dose (LD50) in mice was 5.48 g/kg bw, almost 2740 times the clinical dose in humans. Among the five indole alkaloids, the maximum tolerance dose in mice ranged from 0.75 to 4 g/kg bw. The TA-treated rats did not die and showed no adverse effects or dose-dependent changes in weight or food and water consumption, despite fluctuations in hematological and biochemical parameters compared with historical data. Furthermore, both gross and histopathological observations revealed no abnormalities in any organ. With daily oral administration to rats, the non-observed-adverse-effect-level of TA was 100 mg/kg bw. The results indicate that TA is safe for clinical use.
引用
收藏
页码:77 / 88
页数:12
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