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Published on: April 6, 2017
Cardamom extract as inhibitor of human platelet aggregation
W Jessie Suneetha1, T P Krishnakantha
1Department of Biochemistry and Nutrition, Central Food Technological Research Institute, Mysore 570 020, India.
Insights
Cardamom extract inhibits human platelet aggregation and lipid peroxidation. This natural compound shows dose-dependent effects, suggesting potential cardioprotective benefits by preventing platelet activation and oxidative damage.
Area of Science:
- Pharmacology
- Cardiovascular Research
- Natural Products
Background:
- Platelet aggregation and lipid peroxidation are key factors in thrombotic and cardiovascular diseases.
- Natural compounds are increasingly investigated for their therapeutic potential in cardiovascular health.
Purpose of the Study:
- To investigate the inhibitory effects of cardamom extract on human platelet aggregation.
- To evaluate the impact of cardamom extract on platelet lipid peroxidation.
Main Methods:
- Human platelet-rich plasma (PRP) and platelet membranes were used.
- Platelet aggregation was induced by agonists like ADP, epinephrine, collagen, and calcium ionophore A23187.
- Lipid peroxidation was assessed using malondialdehyde (MDA) levels.
Main Results:
- Cardamom extract demonstrated significant inhibitory activity against platelet aggregation induced by ADP, epinephrine, collagen, and calcium ionophore A23187.
- The inhibitory effect was dose-dependent and time-dependent.
- Cardamom extract significantly reduced MDA formation, indicating decreased lipid peroxidation.
Conclusions:
- Aqueous cardamom extract possesses components that inhibit human platelet aggregation.
- Cardamom extract may protect platelets against lipid peroxidation, suggesting a potential role in cardiovascular disease prevention.
Abstract:
The inhibitory activity of cardamom extract was studied on human platelets. Platelet aggregation and lipid peroxidation were evaluated with platelet rich plasma (PRP) and platelet membranes, respectively, obtained from blood of healthy volunteers. Human platelets were subjected to stimulation with a variety of agonists including ADP (2.5 mM), epinephrine (2.5 mM), collagen (10 mM), calcium ionophore A 23187 (6 microM) and ristocetin (1.25 microg/mL). The IC50 were 0.49, 0.21, 0.55 and 0.59 mg with ADP, epinephrine, collagen and calcium ionophore A 23187, respectively, and no inhibition with ristocetin. The inhibitory effect was dose dependent with concentrations varying between 0.14 and 0.70 mg and time dependent at IC50. Lipid peroxidation induced by iron--ascorbic acid system in platelet membranes was analysed with malondialdehyde (MDA) as an index. An increase in concentration of cardamom has decreased the MDA formation significantly. Hence, it may be said that aqueous extract of cardamom may have component(s), which protect platelets from aggregation and lipid peroxidation.
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