Ming-Yi Shen

Prof. Ming-Yi Shen

Graduate Institute of Biomedical Sciences, China Medical University, Taiwan
orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 April 2003 in Journal of Agricultural and Food Chemistry
Verified
Journal Article
Closed access
GHGeorge Hsiao
George Hsiao
Ming-Yi ShenMing-Yi Shen
Ming-Yi Shen
KLKuan-Hung Lin
Kuan-Hung Lin
MLMing-Huang Lan
Ming-Huang Lan
LWLi-Yu Wu
Li-Yu Wu
JSJoen-Rong Sheu
Joen-Rong Sheu

1 October 2007 in British Journal of Haematology
Verified
Journal Article
Open access
PDF file
Ming-Yi ShenMing-Yi Shen
Ming-Yi Shen
GHGeorge Hsiao
George Hsiao
CLChang L. Liu
Chang L. Liu
TFTsorng H. Fong
Tsorng H. Fong
KLKuang H. Lin
Kuang H. Lin
Joen-Rong SheuJoen-Rong Sheu
Joen-Rong Sheu
Summary: Resveratrol has been reported to have antiplatelet activity; however, the detailed mechanisms have not yet been resolved. This study aimed to systematically examine the detailed mechanisms of resveratrol in the prevention of platelet activation in vitro and in vivo. Resveratrol (0·05–0·25 μmol/l) showed stronger inhibition of platelet aggregation stimulated by collagen (1 μg/ml) than other agonists. Resveratrol (0·15 and 0·25 μmol/l) inhibited collagen‐induced platelet activation accompanied by [Ca+2]i mobilization, thromboxane A2 (TxA2) formation, phosphoinositide breakdown, and protein kinase C (PKC) activation. Resveratrol markedly increased levels of NO/cyclic guanosine monophosphate (GMP), and cyclic GMP‐induced vasodilator‐stimulated phosphoprotein phosphorylation. Resveratrol markedly inhibited p38 mitogen‐activated protein kinase (MAPK) but not Jun N‐terminal kinase or extracellular signal‐regulated kinase‐2 phosphorylation in washed platelets. Resveratrol‐reduced hydroxyl radical (OH−) formation in the electron spin resonance study. In an in vivo study, resveratrol (5 mg/kg) significantly prolonged platelet plug formation of mice. In conclusion, the main findings of this study suggest that the inhibitory effects of resveratrol possibly involve (i) inhibition of the p38 MAPK‐cytosolic phospholipase A2‐arachidonic acid‐TxA2‐[Ca+2]i cascade and (ii) activation of NO/cyclic GMP, resulting in inhibition of phospholipase C and/or PKC activation. Resveratrol is likely to exert significant protective effects in thromboembolic‐related disorders by inhibiting platelet aggregation.

19 June 2004 in Journal of Agricultural and Food Chemistry
Verified
Journal Article
Closed access
Joen-Rong SheuJoen-Rong Sheu
Joen-Rong Sheu
GHGeorge Hsiao
George Hsiao
PCPo-Hsiu Chou
Po-Hsiu Chou
Ming-Yi ShenMing-Yi Shen
Ming-Yi Shen
DCDuen-Suey Chou
Duen-Suey Chou

1 September 2004 in British Journal of Pharmacology
Verified
Journal Article
Closed access
PDF file
Joen-Rong SheuJoen-Rong Sheu
Joen-Rong Sheu
TFTsorng H Fong
Tsorng H Fong
CLCheng M Liu
Cheng M Liu
Ming-Yi ShenMing-Yi Shen
Ming-Yi Shen
TCTa L Chen
Ta L Chen
GHGeorge Hsiao
George Hsiao

10 March 2016 in Blood
Verified
Journal Article
Open access
PDF file
Ming-Yi ShenMing-Yi Shen
Ming-Yi Shen
FCFang-Yu Chen
Fang-Yu Chen
JHJing-Fang Hsu
Jing-Fang Hsu
RFRu-Huei Fu
Ru-Huei Fu
CCChia-Ming Chang
Chia-Ming Chang
CCChu-Huang Chen
Chu-Huang Chen
Key Points: L5 is elevated in ischemic stroke patients, and its receptor, LOX-1, plays a critical role in increasing stroke size. L5 induces platelet secretion of Aβ to potentiate platelet activation and aggregation via LOX-1 and IKK2.

21 November 2013 in Blood
Verified
Journal Article
Open access
PDF file
HCHua-Chen Chan
Hua-Chen Chan
Liang-Yin KeLiang-Yin Ke
Liang-Yin Ke
CCChih-Sheng Chu
Chih-Sheng Chu
AN-SHENG Sean LeeAN-SHENG Sean Lee
AN-SHENG Sean Lee
Ming-Yi ShenMing-Yi Shen
Ming-Yi Shen
CCChu-Huang Chen
Chu-Huang Chen
Key Points: Highly electronegative LDL (L5), which is elevated in patients with STEMI, induces platelet activation and aggregation through LOX-1. L5 may have a role in promoting thrombogenesis that leads to STEMI.