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Synthesis of huaicarbon A/B and their activating effects on platelet glycoprotein VI receptor to mediate collagen-induced platelet aggregation.
Yu, Hongli; Chen, Yeqing; Wu, Hao; Wang, Kuilong; Liu, Liping; Zhang, Xingde.
Affiliation
  • Yu H; School of Pharmacy, Nanjing University of Chinese MedicineNanjing 210023, P. R. China; Jiangsu Key Laboratory of Chinese Medicine Processing, Nanjing University of Chinese MedicineNanjing 210023, P. R. China; Engineering Center of State Ministry of Education for Standardization of Chinese Medicine P
  • Chen Y; School of Pharmacy, Nanjing University of Chinese Medicine Nanjing 210023, P. R. China.
  • Wu H; School of Pharmacy, Nanjing University of Chinese MedicineNanjing 210023, P. R. China; Jiangsu Key Laboratory of Chinese Medicine Processing, Nanjing University of Chinese MedicineNanjing 210023, P. R. China; Engineering Center of State Ministry of Education for Standardization of Chinese Medicine P
  • Wang K; School of Pharmacy, Nanjing University of Chinese Medicine Nanjing 210023, P. R. China.
  • Liu L; School of Pharmacy, Nanjing University of Chinese Medicine Nanjing 210023, P. R. China.
  • Zhang X; School of Pharmacy, Nanjing University of Chinese Medicine Nanjing 210023, P. R. China.
Am J Transl Res ; 9(2): 499-506, 2017.
Article in En | MEDLINE | ID: mdl-28337278
ABSTRACT
Quercetin and rhamnose were efficiently converted into huaicarbon A/B by heating at 250°C for 10-15 min or at 200°C for 25-30 min. With the optimum molar ratio of quercetin/rhamnose (13), huaicarbon A and B yields reached 25% and 16% respectively after heating at 250°C, with 55% quercetin conversion. Huaicarbon A/B both promoted washed platelet aggregation dose-dependently, which was antagonized by an inhibitor of glycoprotein VI (GPVI) receptor. Similarly, they both promoted collagen-induced platelet aggregation in platelet-rich plasma in dose-dependent manners. According to the S type dose-response model, EC50 values of huaicarbon A and huaicarbon B were calculated as 33.48 µM and 48.73 µM respectively. They induced intracellular Ca2+ accumulation that was specifically blocked by GPVI antagonist. Huaicarbon A/B enhanced intracellular Ca2+ accumulation and facilitated collagen-induced platelet aggregation, which were blocked by GPVI antagonist. They were conducive to collagen-induced platelet aggregation by activating platelet GPVI receptor.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Am J Transl Res Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Am J Transl Res Year: 2017 Document type: Article
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