毒性
慢性毒性
组织病理学
紫苏
急性毒性
医学
药理学
不利影响
未观察到不良反应水平
生理学
毒理
化学
内科学
生物
病理
有机化学
原材料
作者
Huixing Zhang,Yi‐Hong Tian,Jian Guan,Qiang-min Xie,Yuqing Zhao
摘要
Abstract BACKGROUND Perilla seed oil (PSO) is the main constituent of perilla seeds currently being used in the food industry, however it also has great clinical potential in the regulation of lung function as a nutrition supplement because of the high content of α ‐linolenic acid (ALA). In this study, the pharmacological activities including anti‐tussive, expectorant and anti‐inflammatory effect of PSO were performed. Furthermore, the 90‐day sub‐chronic oral toxicity with a 30 day recovery period was evaluated in Wistar rats. RESULTS The pharmacological studies demonstrated that PSO inhibited cough frequency induced by capsaicine in mice. PSO also inhibited the leukotriene B4 (LTB4) release from the calcium ionophore A23187‐induced polymorphonuclear neutrophils (PMNs) to some extent. In this sub‐chronic toxicity study, mortality, clinical signs, body weight, food consumption, hematology, serum biochemistry, urinalysis, organ weight, necropsy, and histopathology were used to evaluate the toxicity of PSO. Lower body weight and various negative impacts on liver related parameters without histopathological lesion were observed in the 16 g kg −1 groups. No clinically significant changes were discovered in the 4 g kg −1 group during the test period. CONCLUSION In summary, PSO exhibited anti‐tussive and anti‐inflammatory activities in vivo and in vitro . These sub‐chronic toxicity studies inferred that the ‘no‐observed adverse effect level’ (NOAEL) of PSO in Wistar rats was determined to be 4 g kg −1 . These results may provide a safety profile and a valuable reference for the use of PSO. © 2020 Society of Chemical Industry
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