Li, Sw., Feng, X., Xu, H. et al. Comparison on Anticoagulation and Antiplatelet Aggregation Effects of Puerarin with Heparin Sodium and Tirofiban Hydrochloride: An In Vitro Study., Chin. J. Integr. Med. 24, 103–108 (2018). https://doi.org/10.1007/s11655-017-2419-7
Si-wei Li, Xue Feng, Hao Xu, et al. Comparison on Anticoagulation and Antiplatelet Aggregation Effects of Puerarin with Heparin Sodium and Tirofiban Hydrochloride: An In Vitro Study[J]. Chinese Journal of Integrative Medicine, 2018,24(2):103-108.
Li, Sw., Feng, X., Xu, H. et al. Comparison on Anticoagulation and Antiplatelet Aggregation Effects of Puerarin with Heparin Sodium and Tirofiban Hydrochloride: An In Vitro Study., Chin. J. Integr. Med. 24, 103–108 (2018). https://doi.org/10.1007/s11655-017-2419-7DOI:
Si-wei Li, Xue Feng, Hao Xu, et al. Comparison on Anticoagulation and Antiplatelet Aggregation Effects of Puerarin with Heparin Sodium and Tirofiban Hydrochloride: An In Vitro Study[J]. Chinese Journal of Integrative Medicine, 2018,24(2):103-108. DOI: 10.1007/s11655-017-2419-7.
Comparison on Anticoagulation and Antiplatelet Aggregation Effects of Puerarin with Heparin Sodium and Tirofiban Hydrochloride: An In Vitro Study
摘要
To detect the anticoagulation and antiplatelet effects of different concentrations of puerarin
heparin sodium and tirofiban hydrochloride on the blood samples of healthy volunteers by Sonoclot coagulation and platelet function analyzer. Peripheral blood samples were extracted from 20 healthy volunteers
followed by adding different concentrations of puerarin
heparin sodium and tirofiban hydrochloride. Samples were detected for activated clotting time (ACT)
clot rate (CR) and platelet function (PF) by Sonoclot coagulation and platelet function analyzer instrument. For puerarin and heparin sodium
the values of ACT gradually increased
and the values of CR and PF gradually decreased with increasing in drug concentration. There was a linear (or log linear) relationship between ACT
CR
PF value and drug concentration (P<0.01). Corresponding to each value
a regression equation was obtained. For tirofiban hydrochloride
the values of ACT and CR had no significant changes
while PF values gradually decreased with concentration increasing. There was also a linear relationship between PF values and concentrations of tirofiban hydrochloride (P<0.01). Under the same ACT values
the puerarin corresponding CR values (CR = e−0.0062ACT+4.31
P<2.2e-16) were always higher than the corresponding values (CR = e−0.0028ACT+2.79
P-value<2.2e-16) of heparin sodium. For high concentrations of puerarin (e.g. 3.8 mg/600 μL) and tirofiban hydrochloride (e.g. 0.8 μg/600 μL)
PF values had no significant difference. However
PF values for high puerarin concentration had a larger variance. Puerarin has similar anticoagulant and antiplatelet effects with the heparin sodium
and may have a lower hemorrhage risk than heparin sodium when obtained the same anticoagulation effect in the concentration range of this experiment. In addition
for high concentration
puerarin had the same antiplatelet function as tirofiban hydrochloride but with a larger individual variability.
Abstract
To detect the anticoagulation and antiplatelet effects of different concentrations of puerarin
heparin sodium and tirofiban hydrochloride on the blood samples of healthy volunteers by Sonoclot coagulation and platelet function analyzer. Peripheral blood samples were extracted from 20 healthy volunteers
followed by adding different concentrations of puerarin
heparin sodium and tirofiban hydrochloride. Samples were detected for activated clotting time (ACT)
clot rate (CR) and platelet function (PF) by Sonoclot coagulation and platelet function analyzer instrument. For puerarin and heparin sodium
the values of ACT gradually increased
and the values of CR and PF gradually decreased with increasing in drug concentration. There was a linear (or log linear) relationship between ACT
CR
PF value and drug concentration (P<0.01). Corresponding to each value
a regression equation was obtained. For tirofiban hydrochloride
the values of ACT and CR had no significant changes
while PF values gradually decreased with concentration increasing. There was also a linear relationship between PF values and concentrations of tirofiban hydrochloride (P<0.01). Under the same ACT values
the puerarin corresponding CR values (CR = e−0.0062ACT+4.31
P<2.2e-16) were always higher than the corresponding values (CR = e−0.0028ACT+2.79
P-value<2.2e-16) of heparin sodium. For high concentrations of puerarin (e.g. 3.8 mg/600 μL) and tirofiban hydrochloride (e.g. 0.8 μg/600 μL)
PF values had no significant difference. However
PF values for high puerarin concentration had a larger variance. Puerarin has similar anticoagulant and antiplatelet effects with the heparin sodium
and may have a lower hemorrhage risk than heparin sodium when obtained the same anticoagulation effect in the concentration range of this experiment. In addition
for high concentration
puerarin had the same antiplatelet function as tirofiban hydrochloride but with a larger individual variability.
Yin ZZ, Zeng GY. Pharmacology of puerarin. V. Effects of puerarin on platelet aggregation and release of 5-HT from platelets. Acta Acad Med Sin (Chin) 1981;3 Suppl 1:44–47.
Tuman KJ, Spiess BD, Mccarthy RJ, Ivankovich AD. Comparison of viscoelastic measures of coagulation after cardiopulmonary bypass. Anesth Analg 1989;69:69–75.
Chapin JW, Becker GL, Hulbert BJ, Newland MC, Cuka DJ, Wood RP, et al. Comparison of thromboelastograph and Sonoclot coagulation analyzer for assessing coagulation status during orthotopic liver transplantation. Transplant Proc 1989;21:3539–3539.
John JD, William AL, AJ Wright. Effective hemostasis in cardiac surgery. Anesthesiology 1989;71:325–326.
Yang X. The study of development of purring injection [dissertation]. Changchun: Jilin University; 2008.
Induction of adhesion molecule expression in co-culture of human bronchial epithelial cells and neutrophils suppressed by puerarin via down-regulating p38 mitogen-activated protein kinase and nuclear factor κB pathways
In vitro and in vivo effects of puerarin on promotion of osteoblast bone formation
Effect of puerarin on the release of interleukin-8 in co-culture of human bronchial epithelial cells and neutrophils
Puerarin improve insulin resistance of adipocyte through activating Cb1 binding protein path
In vivo and in vitro antiviral effects of berberine on influenza virus
相关作者
暂无数据
相关机构
Deparment of Laboratory Medicine, Wenzhou Medical College
Department of Clinical Laboratory, Chinese People’s Liberation Army General Hospital
Department of Orthopedics, the Second Affiliated Hospital of Medical College of Xi’an Jiaotong University
Department of Orthopedics, the Second Hospital of Tsinghua University
Department of Orthopedics, Shaanxi Provincial People’s Hospital