In Vitro Assay of Quinoa (Chenopodium quinoa Willd.) and Lupin (Lupinus spp.) Extracts on Human Platelet Aggregation.

Antiplatelet Cardiovascular risk Chenopodium quinoa Willd. Lupinus spp. Plant crops Plant extracts Platelet aggregation

Journal

Plant foods for human nutrition (Dordrecht, Netherlands)
ISSN: 1573-9104
Titre abrégé: Plant Foods Hum Nutr
Pays: Netherlands
ID NLM: 8803554

Informations de publication

Date de publication:
Jun 2020
Historique:
pubmed: 23 2 2020
medline: 5 6 2020
entrez: 23 2 2020
Statut: ppublish

Résumé

Cardiovascular disease (CVD) is the leading cause of death throughout the world. A major risk factor for CVD is platelet aggregation. Various plant extracts exhibit anti-aggregatory action in vitro. The dietary intake of traditional plant crops such as quinoa (Chenopodium quinoa Willd) and lupin (Lupinus spp., Fabaceae family), highly recognized for their high nutritional value, is increasing worldwide. The aim of the study was to assay possible antiplatelet effects of quinoa and lupin bean extracts in vitro. The proximate chemical composition of quinoa grains and the three most widely known lupin cultivars: blue (L. angustifolius), yellow (L. luteus or mutabilis) and white (L. albus) grown in Chile were analyzed. The anti-aggregation activity of the ethanol extracts of the crops was assayed using flow cytometry in ADP-stimulated human platelets, and their inhibition of the maximal platelet aggregation was measured. All the lupin extracts exhibited a significant anti-aggregatory effect (p < 0.0001), while quinoa extracts did not exert this effect compared to control platelets. In conclusion, lupin beans extracts exhibited an anti-aggregatory effect on activated human platelets.

Identifiants

pubmed: 32086676
doi: 10.1007/s11130-019-00786-y
pii: 10.1007/s11130-019-00786-y
doi:

Substances chimiques

Plant Extracts 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

215-222

Auteurs

Marcelo Alarcón (M)

Thematic Task Force on Aging, CUECH Research Network, Santiago, Chile.
Thrombosis Research Center, Department of Clinical Biochemistry and Immunohematology, Faculty of Health Sciences and Interdisciplinary Excellence Research Program on Healthy Ageing (PIEI-ES), Universidad de Talca, 2 Norte 685, Talca, Chile.

Michelle Bustos (M)

Thrombosis Research Center, Department of Clinical Biochemistry and Immunohematology, Faculty of Health Sciences and Interdisciplinary Excellence Research Program on Healthy Ageing (PIEI-ES), Universidad de Talca, 2 Norte 685, Talca, Chile.

Diego Mendez (D)

Thrombosis Research Center, Department of Clinical Biochemistry and Immunohematology, Faculty of Health Sciences and Interdisciplinary Excellence Research Program on Healthy Ageing (PIEI-ES), Universidad de Talca, 2 Norte 685, Talca, Chile.

Eduardo Fuentes (E)

Thematic Task Force on Aging, CUECH Research Network, Santiago, Chile.
Thrombosis Research Center, Department of Clinical Biochemistry and Immunohematology, Faculty of Health Sciences and Interdisciplinary Excellence Research Program on Healthy Ageing (PIEI-ES), Universidad de Talca, 2 Norte 685, Talca, Chile.

Ivan Palomo (I)

Thematic Task Force on Aging, CUECH Research Network, Santiago, Chile. ipalomo@utalca.cl.
Thrombosis Research Center, Department of Clinical Biochemistry and Immunohematology, Faculty of Health Sciences and Interdisciplinary Excellence Research Program on Healthy Ageing (PIEI-ES), Universidad de Talca, 2 Norte 685, Talca, Chile. ipalomo@utalca.cl.

Mariane Lutz (M)

Thematic Task Force on Aging, CUECH Research Network, Santiago, Chile. mariane.lutz@uv.cl.
Interdisciplinary Center for Health Studies, CIESAL, Faculty of Medicine, Universidad de Valparaíso, Viña del Mar, Chile. mariane.lutz@uv.cl.

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