Journal
JOURNAL OF ETHNOPHARMACOLOGY
Volume 278, Issue -, Pages -Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2021.114306
Keywords
Amebia euchroma (Royle) IMJohnst; Hemostasis; Bleeding time; Platelet
Categories
Funding
- Science and Technology Major Projects: Significant New-Drugs Creation [XJDX0208-2006-01]
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The ethyl acetate extract of Arnebia euchroma showed potential hemostatic effects in mice by shortening bleeding and clotting time, increasing platelet count, inducing platelet aggregation, adhesion, and PF-4 secretion, as well as increasing fibrinogen levels while shortening TT.
Ethnopharmacological relevance: Arnebia euchroma (Boyle) I.M.Johnst (AE) has been reported to be a potentially useful medicinal herb for the treatment of several circulatory diseases in traditional Chinese medicine. It shows effects such as cooling of the blood, promotion of blood circulation, detoxification, and rash clearance. Aim of the study: To explore the hemostatic effect of the ethyl acetate extract of AE in mice. Materials and methods: In this study, we explored the effects of AE on bleeding time, blood coagulation time, platelet count, and blood coagulation parameters in normal Kunming mice. Different doses of the AE extract (5, 10, and 20 g kg(-1).day(-1)) were administered to mice for 14 days. Sodium carboxymethyl cellulose (CMC-Na at 0.5%) and Yunnan Baiyao (0.8 g kg(-1).day(-1)) were administered as negative and positive control treatments, respectively. Bleeding time, blood coagulation time, platelet count, blood platelet aggregation, blood platelet adhesion to fibrinogen, platelet factor 4 (PF-4) secretions from blood platelets, and blood coagulation parameters including prothmmbin time (PT), activated partial thromboplastin time (aPTT), thrombin time (TT), and fibrinogen (FIB) levels were measured on day 15 of administration. Results: Bleeding and blood coagulation time were significantly lower and TT was shorter in the AE extract-treated groups than in the control groups. Furthermore, FIB levels and platelet count were higher, whereas blood platelet aggregation, blood platelet adhesion to fibrinogen, and PF-4 secretion from blood platelets were more obvious in the AE extract-treated groups than in the control group. However, no significant differences were detected for PT and aPTT between the extract-treated and control groups. Conclusions: The ethyl acetate extract of AE showed potential hemostasis effects in mice by shortening the bleeding and coagulation time. In addition, the extract increased platelet count and induced blood platelet aggregation, blood platelet adhesion to fibrinogen, PF-4 secretion from blood platelets, and FIB level, while it shortened TT.
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