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Morus alba extract modulates blood pressure homeostasis through eNOS signaling
Author(s) -
Carrizzo Albino,
Ambrosio Mariateresa,
Damato Antonio,
Madonna Michele,
Storto Marianna,
Capocci Luca,
Campiglia Pietro,
Sommella Eduardo,
Trimarco Valentina,
Rozza Francesco,
Izzo Raffaele,
Puca Annibale A.,
Vecchione Carmine
Publication year - 2016
Publication title -
molecular nutrition and food research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.495
H-Index - 131
eISSN - 1613-4133
pISSN - 1613-4125
DOI - 10.1002/mnfr.201600233
Subject(s) - enos , homeostasis , blood pressure , medicine , chemistry , biology , nitric oxide , nitric oxide synthase
Scope Morus alba is a promising phytomedicine cultivated in oriental countries that is extensively used to prevent and treat various cardiovascular problems. To date, despite its beneficial effects, the molecular mechanisms involved remain unclear. Thus, we investigate the vascular and haemodynamic effects of Morus alba extract in an experimental model focusing our attention on the molecular mechanisms involved. Methods and results Through vascular reactivity studies, we demonstrate that Morus alba extract evokes endothelial vasorelaxation through a nitric oxide‐dependent pathway. Our molecular analysis highlights an increase in endothelial nitric oxide synthase (eNOS) phosphorylation. In vivo administration of Morus alba extract reduces blood pressure levels exclusively in wild‐type mice, whereas it fails to evoke any haemodynamic effects in eNOS‐deficient mice. Molecular analyses revealed that its beneficial action on vasculature is mediated by the activation of two important proteins that act as stress sensors and chaperones: PERK and heat shock protein 90. Finally, Morus alba extract exerts antihypertensive action in an experimental model of arterial hypertension. Conclusion Through its action on eNOS signaling, Morus alba extract could act as a food supplement for the regulation of cardiovascular system, mainly in clinical conditions characterized by eNOS dysfunction, such as arterial hypertension.