4.6 Article

Aged Garlic Extract Inhibits Human Platelet Aggregation by Altering Intracellular Signaling and Platelet Shape Change

Journal

JOURNAL OF NUTRITION
Volume 146, Issue 2, Pages 410S-415S

Publisher

OXFORD UNIV PRESS
DOI: 10.3945/jn.114.202408

Keywords

garlic; platelet aggregation; GPIIb/Illa receptor; cAMP; fibrinogen; thrombosis

Funding

  1. University of California, Los Angeles School of Medicine
  2. University of Florida
  3. American Botanical Council
  4. American Herbal Products Association
  5. ASN
  6. Japanese Society for Food Factors
  7. Japan Society for Bioscience, Biotechnology, and Agrochemistry
  8. Japan Society of Nutrition and Food Science
  9. Natural Products Association
  10. Wakunaga of America Co., Ltd.

Ask authors/readers for more resources

Background: Increased platelet aggregation plays a pivotal role in the etiology of cardiovascular disease. Upon platelet aggregation, an increase in free cytoplasmic Ca2+ results in the inhibition of soluble guanylyl cyclase (sGC) and adenylyl cyclase (AC), leading to a decrease in cyclic guaninosine-5'-monophosphate (cGMP) and cAMP, respectively. This leads to the activation of the glycoprotein I lb/I I la (GPIlb/111a) fibrinogen receptor, resulting in platelet shape change. Aged garlic extract (AGE) decreases platelet aggregation; however, the mechanisms involved are not clearly defined. Objective: Our objective was to investigate the effects of AGE on intraplatelet cell signaling and platelet shape change. Methods: Platelets from 14 participants were studied. Platelet aggregation was induced by ADP in the presence of AGE up to a concentration of 6.25% (vol:vol) alone or in combination with 3-morpholinosydnonimine (Sin -1), a nitric oxide donor. The experiments with AGE were repeated in the presence of 3-isobuty1-1-methylxanthine (IBMX), a phosphodiesterase inhibitor. In a series of separate experiments, platelet aggregation was induced in the presence of either 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ), an sGC inhibitor, or 9-(tetrahydro-2-furanyI)-9H-purin-6-amine (SQ22536), an AC inhibitor, or a combination of both in the presence of IBMX and AGE. Intraplatelet cGMP and cAMP were measured. The platelets were also subjected to scanning electron microscopic analysis, and their binding to fibrinogen was determined. Results: AGE decreased platelet aggregation at all concentrations tested; this decrease was more marked in the presence of Sin -1 and ranged between 15% and 67%. The presence of IBMX also led to a decrease (17-35%) in platelet aggregation at all AGE concentrations and a significant decrease in the amounts of cGMP (24-41%) and cAMP (19-70%), respectively, in the presence of ODQ and SQ22536. The presence of AGE significantly inhibited the binding of activated platelets to fibrinogen, preventing changes in platelet shape. Conclusion: These results indicate that AGE inhibits platelet aggregation by increasing cyclic nucleotides and inhibiting fibrinogen binding and platelet shape change.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available