2014
DOI: 10.1016/j.jff.2013.11.008
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Involvement of nitric oxide and prostacyclin in the antihypertensive effect of low-molecular-weight procyanidin rich grape seed extract in male spontaneously hypertensive rats

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Cited by 35 publications
(16 citation statements)
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“…The anti‐hypertensive effect of grape seed flavanols in SHR is an endothelium‐dependent effect mainly mediated by changes in endothelium‐derived factors such as nitric oxide and prostacyclin . Therefore, it would seem plausible that the endothelium of SHR presents higher concentrations of flavanol metabolites than that from healthy animals.…”
Section: Discussionmentioning
confidence: 99%
“…The anti‐hypertensive effect of grape seed flavanols in SHR is an endothelium‐dependent effect mainly mediated by changes in endothelium‐derived factors such as nitric oxide and prostacyclin . Therefore, it would seem plausible that the endothelium of SHR presents higher concentrations of flavanol metabolites than that from healthy animals.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, several studies have reported the antihypertensive effects of GSPE and its underlying mechanism in hypertensive rats. For instance, Quiñones et al showed that GSPE increased prostaglandin F1α, a stable indicator of the production of prostaglandin I2, which is a vasodilator and inhibitor of platelet aggregation [60]. Liu et al showed that GSPE decreased the expression of both ET-1, a known contributor to vasoconstriction and vascular remodeling, and transforming growth factor-β, which stimulates ET-1 expression and renin release [61,62].…”
Section: Discussionmentioning
confidence: 99%
“…The antihypertensive properties of PAs are related to NOmediated vasodilation [61], angiotensin converting enzyme (ACE) inhibition [62] and a reduction in oxidative stress [59]. Nonetheless, the blood pressure-lowering effect of flavanols is mainly mediated through the NO pathway, and for grape seed PAs, it is also partially mediated by prostacyclin [63]. Other mechanisms that may be involved in the vasodilator effect of PAs include the inhibition of both phosphodiesterases (PDEs) 2 and 4, which catalyze the degradation of cAMP and cGMP, and PDE-5, which degrades cGMP [64].…”
Section: Pa Effects In Hypertensionmentioning
confidence: 99%