Licorice is used as a medicinal plant, and several studies have shown that licorice has beneficial effects. The objective of this study was to evaluate the safety of nonpolar licorice extract using toxicity experiments. Nonpolar extract from the root of Glycyrrhiza uralensis (NERG) was analyzed by high-performance liquid chromatography (HPLC). Antioxidant ability was determined by method of TPC and DPPH. Blood pressure was monitored by using blood pressure meter. In the acute study, a single dose (2,000 mg/kg) was orally administered to mice. In the subchronic study, mice were treated with extract at doses (50, 100, 500, and 1,000 mg/kg) for 120 days.Significantly difference was not shown at blood pressure, hematological, and biochemical parameters, and histopathology on mice. The results suggested that at acute and subchronic toxicity, each levels of nonpolar licorice extract administration in experiments did not cause toxicity effects or death on mice. K E Y W O R D S acute toxicity, de-glycyrrhizin, licorice, nonpolar extract, subchronic toxicity, toxicology | 2243 KIM et al.
2017). Since information about the toxicity of licorice extract is limited, it is important to conduct studies to assess the safety of nonpolar licorice root extract. Therefore, the objective of this study was to evaluate the safety of nonpolar licorice root extract in mice by utilizing acute and subchronic toxicity tests. Our aim is to provide valuable information regarding the usage of this extract.
| MATERIAL S AND ME THODS
| Plant material, preparation of extraction, and administration of extractThe root of licorice was obtained from Deagwang korean plant sales, Chuncheon, Korea. The specimen of G. uralensis was confirmed to Seoul national university and deposited in the Regional Innovation Center (RIC; #040322) of the Hallym University, Chuncheon.The plant root was air-dried and then soaked in a mixture of solvent (Hexane:Ethanol = 9:1) for 24 hr. After 24 hr, the extraction was filtered and concentrated at 37°C using a rotary evaporator (Vacuubrand, CVC 3000). The nonpolar extract from the root of G. uralensis (NERG) was administered orally, in the shape of a pellet, for the acute and subchronic toxicity studies.
| Chemical and reagentsAll chemicals were analytical grade. Acetonitrile was acquired from J. T. Baker Chemical Company. Acetic acid, Folin-Ciocalteu phenol reagent, and 2,2-diphenyl-1-picrylhydrazyl (DPPH) were purchased from Sigma Chemical Company.