Cardamom extract as inhibitor of human platelet aggregation

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 µm) and ristocetin (1.25 µg/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. Copyright © 2005 John Wiley & Sons, Ltd.

[1]  B. Lokesh,et al.  Studies on spice principles as antioxidants in the inhibition of lipid peroxidation of rat liver microsomes , 1992, Molecular and Cellular Biochemistry.

[2]  E. D’Amico,et al.  Effects of catechins on human blood platelet aggregation and lipid peroxidation , 1999, Phytotherapy research : PTR.

[3]  M. D. Peck Interaction of lipids with immune function I: Biochemical effects of dietary lipids on plasma membranes , 1994 .

[4]  J. Heemskerk,et al.  Calcium signalling in platelets and other cells. , 1994, Platelets.

[5]  W. Huestis,et al.  Effects of exogenous phospholipids on platelet activation. , 1993, Biochimica et biophysica acta.

[6]  B. Halliwell,et al.  The role of oxygen radicals in human disease, with particular reference to the vascular system. , 1993, Haemostasis.

[7]  J. Scott,et al.  Dimeric ristocetin flocculates proteins, binds to platelets, and mediates von Willebrand factor-dependent agglutination of platelets. , 1991, The Journal of biological chemistry.

[8]  David R. Phillips,et al.  GPIIb-IIIa: The responsive integrin , 1991, Cell.

[9]  D. Miller,et al.  Studies of ascorbate-dependent, iron-catalyzed lipid peroxidation. , 1989, Archives of biochemistry and biophysics.

[10]  S. Rattan Science behind spices: inhibition of platelet aggregation and prostaglandin synthesis. , 1988, Bioessays.

[11]  M. Maguire,et al.  Vinca alkaloids inhibit conversion of arachidonic acid to thromboxane by human platelet microsomes: comparison with other microtubule-active drugs. , 1987, Biochimica et biophysica acta.

[12]  K. C. Srivastava Effects of aqueous extracts of onion, garlic and ginger on platelet aggregation and metabolism of arachidonic acid in the blood vascular system: in vitro study , 1984 .

[13]  R. Montgomery,et al.  Platelets have more than one binding site for von Willebrand factor. , 1983, The Journal of clinical investigation.

[14]  T. Fujimoto,et al.  Adenosine diphosphate induces binding of von Willebrand factor to human platelets , 1982, Nature.

[15]  J. Gerrard [75] Platelet aggregation and the influence of prostaglandins , 1982 .

[16]  D. Hathaway,et al.  Regulation of human platelet myosin light chain kinase by the catalytic subunit of cyclic AMP-dependent protein kinase , 1981, Nature.

[17]  P. Massini,et al.  Some effects of ionophores for divalent cations on blood platelets. Comparison with the effects of thrombin. , 1974, Biochimica et biophysica acta.