4.6 Article

Inhibitory effect of Campomanesia xanthocarpa in platelet aggregation: Comparison and synergism with acetylsalicylic acid

Journal

THROMBOSIS RESEARCH
Volume 154, Issue -, Pages 42-49

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.thromres.2017.03.020

Keywords

Adenosine diphosphate; Arachidonic acid; Guavirova; Medicinal plants; Nitric oxide

Funding

  1. Programa Institucional de Bolsas de Iniciacao Cientifica - PROBIC/FAPERGS
  2. Instituto de Cardiologia de Cruz Alta (ICCA)
  3. Sulfarma Manipulation Drugstore

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Background and aims: Cardiovascular diseases of thrombotic origin are related to high mortality and standard therapeutic agent used in this case is acetylsalicylic acid (ASA), but serious adverse events may occur. However, recent data has suggested the plant Campomanesia xanthocarpa has antiplatelet activity and could be a viable alternative. In this study we investigated the effects of the encapsulated powder of this plant in human platelet aggregation. Methods: 23 healthy subjects were randomly divided into three groups: (1) ASA (100 mg), (2) C. xanthocarpa (1000 mg) or (3) synergism (500 mg of C. xanthocarpa plush 50 mg of ASA); daily for five days. Antiplatelet activity was determined by turbidimetric method using ADP or arachidonic acid (AA) agonists before, 5 and 8 days after treatments. Results: Treatment with C. xanthocarpa and synergism caused a reduction of 8 +/- 13.5% and 12.5 +/- 5% in platelet aggregation induced by ADP after 5 days of treatment, respectively, returning to basal levels after 8 days. For AA agonist, 5 days of treatment with C. xanthocarpa, ASA or synergism caused a reduction of 46 +/- 15%, 36 +/- 12% and 69.3 +/- 6% in platelet aggregation, respectively, and first two groups returned to baseline values 8 days after treatment ended. Synergism group prolonged antiplatelet effect maintaining aggregation reduction after 8 days the end of treatment. Conclusion: C. xanthocarpa showed antiplatelet action when stimulated by agonist AA, and contributed to the antiplatelet effect when associated with ASA for both agonists, allowing dose reduction to 50 mg. (C) 2017 Elsevier Ltd. All rights reserved.

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