TY - JOUR
T1 - The anti-platelet activity of Hypsizygus marmoreus extract is involved in the suppression of intracellular calcium mobilization and integrin α IIbβ 3 activation
AU - Park, Ji Young
AU - Oh, Won Jun
AU - Kwak, Dong Mi
AU - Kim, Min Gyeong
AU - Seo, Geon Sik
AU - Hong, Seung Bok
AU - Rhee, Man Hee
PY - 2011/6/4
Y1 - 2011/6/4
N2 - Hypsizygus marmoreus are wild and edible mushrooms found in East Asia that are included in the Shimeji family. H. marmoreus have emerged as a pivotal entity and therapeutic target in cardiovascular diseases, but there is little information of their effects on platelet function. Therefore, our study was designed to investigate the effect of this extract on platelet aggregation induced by various agonists, [Ca 2+] i mobilization, extracellular signal-regulated kinase (ERK) phosphorylations, ATP secretion, and integrin α IIbβ 3 activation. We found that H. marmoreus methanol extract dose-dependently inhibited platelet aggregation that was induced by collagen, but not by thrombin or ADP. Collagen-induced intracellular calcium concentration [Ca 2+] i was also dose-dependently suppressed in H. marmoreus extract treated platelets. In addition, collagen-activated ATP secretion was lowered by the H. marmoreus extract treatment. Moreover, H. marmoreus extract was revealed to attenuate fibrinogen binding initiated by collagen. However, ERK phosphorylation was not affected. In conclusion, H. marmoreus extract inhibit platelet aggregation induced by collagen, intracellular calcium mobilization, and dense granule secretion while suppressing integrin α IIbβ 3 activation. Finally, this suggests that H. marmoreus could be developed as a functional food or phytomedicine against platelet related cardiovascular disease, including thrombosis, stroke and atherosclerosis.
AB - Hypsizygus marmoreus are wild and edible mushrooms found in East Asia that are included in the Shimeji family. H. marmoreus have emerged as a pivotal entity and therapeutic target in cardiovascular diseases, but there is little information of their effects on platelet function. Therefore, our study was designed to investigate the effect of this extract on platelet aggregation induced by various agonists, [Ca 2+] i mobilization, extracellular signal-regulated kinase (ERK) phosphorylations, ATP secretion, and integrin α IIbβ 3 activation. We found that H. marmoreus methanol extract dose-dependently inhibited platelet aggregation that was induced by collagen, but not by thrombin or ADP. Collagen-induced intracellular calcium concentration [Ca 2+] i was also dose-dependently suppressed in H. marmoreus extract treated platelets. In addition, collagen-activated ATP secretion was lowered by the H. marmoreus extract treatment. Moreover, H. marmoreus extract was revealed to attenuate fibrinogen binding initiated by collagen. However, ERK phosphorylation was not affected. In conclusion, H. marmoreus extract inhibit platelet aggregation induced by collagen, intracellular calcium mobilization, and dense granule secretion while suppressing integrin α IIbβ 3 activation. Finally, this suggests that H. marmoreus could be developed as a functional food or phytomedicine against platelet related cardiovascular disease, including thrombosis, stroke and atherosclerosis.
KW - Calcium
KW - Collagen
KW - Hypsizygus marmoreus
KW - Integrin α β3
KW - Mushroom
KW - Platelet aggregation
UR - http://www.scopus.com/inward/record.url?scp=79959822895&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:79959822895
SN - 1996-0875
VL - 5
SP - 2369
EP - 2377
JO - Journal of Medicinal Plants Research
JF - Journal of Medicinal Plants Research
IS - 11
ER -