Tang Rong, Tian Ru-Hua, Cai Jia-Zhong, Wu Jun-Hui, Shen Xiao-Ling, Hu Ying-Jie
a Tropical Medicine Institute, Guangzhou University of Chinese Medicine , Baiyun Qu, Guangzhou , China.
b Pi-Wei Institute, Guangzhou University of Chinese Medicine , Baiyun Qu, Guangzhou , China.
Pharm Biol. 2017 Dec;55(1):1740-1746. doi: 10.1080/13880209.2017.1309556.
The leaves of Cajanus cajan (L.) Millsp. (Fabaceae) have diverse bioactivities, but little safety data are reported.
This study examines the toxicological profiles of C. cajan leaf extracts.
The leaves were extracted by water or 90% ethanol to obtain water or ethanol extract (WEC or EEC). EEC was suspended in water and successively fractionated into dichloroform and n-butanol extracts (DEC and BEC). Marker compounds of the extracts were monitored by high-performance liquid chromatography (HPLC). Kunming mice were administered with a single maximum acceptable oral dose (15.0 g/kg for WEC, EEC and BEC and 11.3 g/kg for DEC) to determine death rate or maximal tolerated doses (MTDs). In sub-chronic toxicity investigation, Sprague-Dawley rats were orally given WEC or EEC at 1.5, 3.0 or 6.0 g/kg doses for four weeks and observed for two weeks after dosing to determine toxicological symptoms, histopathology, biochemistry and haematology.
Flavonoids and stilbenes in the extracts were assayed. In acute toxicity test, no mortality and noted alterations in weight and behavioural abnormality were observed, and the maximum oral doses were estimated as MTDs. In sub-chronic toxicity study, no mortality and significant variances in haematological and biochemical parameters or organ histopathology were observed, but increased kidney weight in 3.0 g/kg WEC- or 3.0 and 6.0 g/kg EEC-treated female rats, and reduced testes and epididymis weight in EEC-treated male rats were recorded. These changes returned to the level of control after recovery period.
Acute and sub-chronic toxicity of Cajanus cajan leaf extracts was not observed.
木豆(豆科)叶具有多种生物活性,但安全性数据报道较少。
本研究考察木豆叶提取物的毒理学特征。
用水或90%乙醇提取木豆叶,得到水提取物或乙醇提取物(WEC或EEC)。将EEC悬浮于水中,依次分离得到二氯甲烷提取物和正丁醇提取物(DEC和BEC)。采用高效液相色谱法(HPLC)监测提取物中的标志性化合物。给昆明小鼠灌胃单次最大可接受口服剂量(WEC、EEC和BEC为15.0 g/kg,DEC为11.3 g/kg),以确定死亡率或最大耐受剂量(MTDs)。在亚慢性毒性研究中,给Sprague-Dawley大鼠分别灌胃1.5、3.0或6.0 g/kg剂量的WEC或EEC,持续4周,给药后观察2周,以确定毒理学症状、组织病理学、生物化学和血液学指标。
对提取物中的黄酮类化合物和芪类化合物进行了测定。在急性毒性试验中,未观察到死亡情况,体重和行为异常也无明显变化,最大口服剂量被估计为MTDs。在亚慢性毒性研究中,未观察到死亡情况,血液学和生化参数或器官组织病理学也无显著差异,但在接受3.0 g/kg WEC或3.0和6.0 g/kg EEC处理的雌性大鼠中,肾脏重量增加,在接受EEC处理的雄性大鼠中,睾丸和附睾重量减轻。恢复期后,这些变化恢复到对照水平。
未观察到木豆叶提取物的急性和亚慢性毒性。