Articles producció científicaBioquímica i Biotecnologia

Evidence that nitric oxide mediates the blood pressure lowering effect of a polyphenol-rich cocoa powder in spontaneously hypertensive rats

  • Dades identificatives

    Identificador:  imarina:5125447
    Autors:  Quinones, M; Muguerza, B; Miguel, M; Aleixandre, A
    Resum:
    The involvement of endothelial-relaxing factors on the antihypertensive effect of a polyphenol-rich cocoa powder named CocoanOX (CCX) was studied. Thirty 17-20-week-old male spontaneously hypertensive rats (SHR), weighing 314 ± 3 g were used. They were divided into two groups of 15 animals, that were respectively administered by gastric intubation distilled water or 300 mg/kg CCX dissolved in distilled water, between 9 am and 10 am. 2 h after the oral administration, 5 of the animals in each group were intraperitoneally administered 1 ml saline. The remaining rats in both groups were divided into another two groups of 5 animals that were respectively administered 30 mg/kg Nw-nitro-l-arginine methyl ester (l-NAME) dissolved in 1 ml of saline or 5 mg/kg indomethacin also dissolved in 1 ml of saline by the same procedure. Systolic blood pressure (SBP) was recorded in the rats by the tail cuff method before the initial oral administration and also 4 h after this administration. CCX caused a significant decrease in SBP (-49.5 ± 4.9 mm Hg; p < 0.05). l-NAME caused a clear increase in SBP in the rats (+16.2 ± 4.3 mm Hg; p < 0.05), and the effect of CCX was not observed in the SHR that were treated with l-NAME (+4.1 ± 1.7 mm Hg; p < 0.05). Nevertheless, indomethacin treatment did not modify SBP in the SHR and this compound failed to modify the antihypertensive effect of CCX in these animals. In conclusion, this study proves the participation of NO in the antihypertensive effect of CCX in the SHR strain. When CCX is administered, the synthesis, or the bioavailability, of this endothelial factor could increase, but other mechanisms may also participate in the antihypertensive effect of this cocoa powder. In any case, further investigation should be carried out to characterize the
  • Altres:

    Autor segons l'article: Quinones, M; Muguerza, B; Miguel, M; Aleixandre, A
    Departament: Bioquímica i Biotecnologia
    Autor/s de la URV: Muguerza Marquínez, Maria Begoña
    Paraules clau: Cocoa; Nitric oxide; Polyphenols; Spontaneously hypertensive rats
    Resum: The involvement of endothelial-relaxing factors on the antihypertensive effect of a polyphenol-rich cocoa powder named CocoanOX (CCX) was studied. Thirty 17-20-week-old male spontaneously hypertensive rats (SHR), weighing 314 ± 3 g were used. They were divided into two groups of 15 animals, that were respectively administered by gastric intubation distilled water or 300 mg/kg CCX dissolved in distilled water, between 9 am and 10 am. 2 h after the oral administration, 5 of the animals in each group were intraperitoneally administered 1 ml saline. The remaining rats in both groups were divided into another two groups of 5 animals that were respectively administered 30 mg/kg Nw-nitro-l-arginine methyl ester (l-NAME) dissolved in 1 ml of saline or 5 mg/kg indomethacin also dissolved in 1 ml of saline by the same procedure. Systolic blood pressure (SBP) was recorded in the rats by the tail cuff method before the initial oral administration and also 4 h after this administration. CCX caused a significant decrease in SBP (-49.5 ± 4.9 mm Hg; p < 0.05). l-NAME caused a clear increase in SBP in the rats (+16.2 ± 4.3 mm Hg; p < 0.05), and the effect of CCX was not observed in the SHR that were treated with l-NAME (+4.1 ± 1.7 mm Hg; p < 0.05). Nevertheless, indomethacin treatment did not modify SBP in the SHR and this compound failed to modify the antihypertensive effect of CCX in these animals. In conclusion, this study proves the participation of NO in the antihypertensive effect of CCX in the SHR strain. When CCX is administered, the synthesis, or the bioavailability, of this endothelial factor could increase, but other mechanisms may also participate in the antihypertensive effect of this cocoa powder. In any case, further investigation should be carried out to characterize the signalling pathways involved in the antihypertensive effect of CCX
    Àrees temàtiques: Astronomia / física; Biodiversidade; Biotecnología; Ciência de alimentos; Ciências biológicas i; Ciências biológicas ii; Ciências biológicas iii; Educação física; Enfermagem; Engenharias ii; Engenharias iv; Farmacia; Interdisciplinar; Medicina i; Medicina ii; Odontología; Pharmacology; Pharmacology & pharmacy; Química
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    Adreça de correu electrònic de l'autor: begona.muguerza@urv.cat
    Data d'alta del registre: 2025-01-25
    Versió de l'article dipositat: info:eu-repo/semantics/acceptedVersion
    Enllaç font original: https://www.sciencedirect.com/science/article/pii/S104366181100171X?via%3Dihub
    Referència a l'article segons font original: Pharmacological Research. 64 (5): 478-481
    Referència de l'ítem segons les normes APA: Quinones, M; Muguerza, B; Miguel, M; Aleixandre, A (2011). Evidence that nitric oxide mediates the blood pressure lowering effect of a polyphenol-rich cocoa powder in spontaneously hypertensive rats. Pharmacological Research, 64(5), 478-481. DOI: 10.1016/j.phrs.2011.06.005
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    DOI de l'article: 10.1016/j.phrs.2011.06.005
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2011
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Pharmacology,Pharmacology & Pharmacy
    Cocoa
    Nitric oxide
    Polyphenols
    Spontaneously hypertensive rats
    Astronomia / física
    Biodiversidade
    Biotecnología
    Ciência de alimentos
    Ciências biológicas i
    Ciências biológicas ii
    Ciências biológicas iii
    Educação física
    Enfermagem
    Engenharias ii
    Engenharias iv
    Farmacia
    Interdisciplinar
    Medicina i
    Medicina ii
    Odontología
    Pharmacology
    Pharmacology & pharmacy
    Química
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