Blockade of glycoprotein IIb/IIIa mediates the antithrombotic activity of butanol fraction of Actinostemma lobatum Maxim

Kim, KH; Lee, HyoJ; Lee, JaeHo; Jang, YuS; Kim, DaeK; Shim, BumS; Cho, KiHo; Ko, SGyu; Ahn, KS; Kim, SH

HERO ID

1457186

Reference Type

Journal Article

Year

2008

Language

English

PMID

18243609

HERO ID 1457186
In Press No
Year 2008
Title Blockade of glycoprotein IIb/IIIa mediates the antithrombotic activity of butanol fraction of Actinostemma lobatum Maxim
Authors Kim, KH; Lee, HyoJ; Lee, JaeHo; Jang, YuS; Kim, DaeK; Shim, BumS; Cho, KiHo; Ko, SGyu; Ahn, KS; Kim, SH
Journal Journal of Ethnopharmacology
Volume 116
Issue 3
Page Numbers 431-438
Abstract <strong>AIM OF THE STUDY: </strong>Actinostemma lobatum Maxim, a wildlife plant of Cucurbitaceae family, has been utilized for the prevention or treatment of cardiovascular diseases as a folk remedy in Korea. However, its scientific evidence remains unclear. Thus, in the present study, we examined the effects of butanol fraction of Actinostemma lobatum Maxim (BFALM) on the in vitro and in vivo antithrombotic activity and possible mechanisms were elucidated for the first time.<br /><br /><strong>MATERIAL AND METHODS: </strong>To elucidate the antithrombotic mechanism of BFALM, platelet aggregation assay, coagulation assay, glycoprotein IIb/IIIa assay, thromboxane A(2) assay and in vivo pulmonary thromboembolism experiment were performed.<br /><br /><strong>RESULTS: </strong>BFALM significantly inhibited collagen, adenosine diphosphate (ADP) and thrombin-induced platelet aggregation in a concentration dependent manner. Consistently, oral administration of BFALM resulted in a dose-dependent increase of survival rates of mice with pulmonary thromboembolism induced by intravenous injection of collagen and epinephrine. In mechanism assays for the antithrombotic activity of BFALM, BFALM significantly inhibited the fibrinogen binding to the platelet surface Glycoprotein IIb/IIIa (GP IIb/IIIa) receptor in a concentration dependent fashion, as well as reduced the level of thromboxane A(2) at 400microg/ml. Furthermore, BFALM significantly prolonged the prothrombin time (PT) and activated partial thromboplastin time (APTT) compared with untreated control.<br /><br /><strong>CONCLUSIONS: </strong>These results suggest that BFALM may exert antithrombotic activity through inhibition of platelet aggregation via GP IIb/IIIa and thromboxane A(2) pathways, along with anticoagulatory activity through intrinsic and extrinsic pathways.
Doi 10.1016/j.jep.2007.12.012
Pmid 18243609
Wosid WOS:000254963500007
Is Certified Translation No
Dupe Override No
Comments Source: Web of Science WOS:000254963500007
Is Public Yes
Language Text English
Keyword Actinostemma lobatum Maxim; platelet aggregation; glycoprotein IIb/IIIa; rutin