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Antiplatelet, antioxidative, and anti-inflammatory effects of hydroquinone.

Mei-Chi ChangBei-En ChangYu-Hwa PanBor-Ru LinYun-Chia LianMing-Shu LeeSin-Yuet YeungLi-Deh LinJiiang-Huei Jeng
Published in: Journal of cellular physiology (2019)
Platelets play crucial roles in thrombosis and hemostasis through platelet activation and aggregation that are crucial in cardiovascular diseases. Hydroquinone (HQ) and its derivatives are present in many dermatological creams, paints, motor fuels, air, microorganisms, and plant products like wheat bread, fruit, coffee, and red wine. The effect of HQ on humans is not clear. In this study, we found that HQ (>25 μM) inhibited arachidonic acid (AA)-induced platelet aggregation. HQ suppressed AA-induced thromboxane B2 production of platelets. HQ (>10 μM) also attenuated ex vivo platelet-rich plasma aggregation. HQ prevented the interleukin (IL)-1β-induced 8-isoprostane, and PGE2 production, but not IL-8 production of pulp cells. These results indicate that HQ may have an antiplatelet effect via inhibition of thromboxane production. HQ has antioxidative and anti-inflammatory effects, and possible inhibition of COX. Exposure and consumption of HQ-containing products, food or drugs may have antiplatelet, antioxidative, and anti-inflammatory effects.
Keyphrases
  • high glucose
  • diabetic rats
  • platelet rich plasma
  • drug induced
  • anti inflammatory
  • induced apoptosis
  • type diabetes
  • oxidative stress
  • cell proliferation
  • pulmonary embolism
  • cardiovascular risk factors