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Antithrombotic Effects of Amaranthus hypochondriacus Proteins in Rats. | LitMetric

Antithrombotic Effects of Amaranthus hypochondriacus Proteins in Rats.

Plant Foods Hum Nutr

Centro de Investigación y Desarrollo en Criotecnología de Alimentos (CIDCA), Calle 47 y 116, 1900, La Plata, Argentina.

Published: March 2016

AI Article Synopsis

  • Cardiovascular disease is a leading cause of disability and early death, and certain diets can help prevent it.
  • The study tested the effects of Amaranthus hypochondriacus proteins on blood clot formation in rats, finding no significant difference in bleeding time compared to control rats but a strong tendency towards inhibition of thrombus formation.
  • Ex-vivo tests showed that amaranth proteins resulted in increased clotting parameters, supporting the idea that they may act as a potential antithrombotic agent.

Article Abstract

Cardiovascular disease (CVD) is a major cause of disability and premature death throughout the world. Diets with antithrombotic components offer a convenient and effective way of preventing and reducing CVD incidence. The aim of the present work was to assess in vivo and ex vivo effects of Amaranthus hypochondriacus proteins on platelet plug formation and coagulation cascade. Amaranth proteins were orally administrated to rats (AG, 8 animals) and bleeding time was determined showing no significant difference compared with control rats (CG, 7 animals). However, results show a strong tendency, suggesting that amaranth proteins are involved in the inhibition of thrombus formation. Non-anticoagulated blood extracted from animals was analyzed with the hemostatometer, where AG parameters obtained were twice the values showed by CG. The clotting tests, thrombin time (TT) and activated partial thromboplastin time (APTT), presented a 17 and 14% clotting formation increase respectively when comparing AG with CG. The ex-vivo assays confirm the hypothesis inferring that amaranth proteins are a potential antithrombotic agent.

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Source
http://dx.doi.org/10.1007/s11130-015-0517-2DOI Listing

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