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Vasorelaxant effect of Alpinia zerumbet's essential oil on rat resistance artery involves blocking of calcium mobilization.

Authors :
Rocha, Danilo Galvão
Holanda, Thais Muratori
Braz, Helyson Lucas Bezerra
de Moraes, João Alison Silveira
Marinho, Aline Diogo
Maia, Pedro Henrique Freitas
de Moraes, Maria Elisabete Amaral
Fechine-Jamacaru, Francisco Vagnaldo
de Moraes Filho, Manoel Odorico
Source :
Fitoterapia. Sep2023, Vol. 169, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

Alpinia zerumbet is a plant from the Zingiberaceae family, popularly used for hypertension treatment. Several studies have demonstrated Alpinia zerumbet vasodilator effect on conductance vessels but not on resistance vessels. Thereby, the aim of this study was to verify the vasodilator effect of the essential oil of Alpinia zerumbet (EOAz) on isolated rat resistance arteries and characterize its mechanism of action. Therefore, the effect of EOAz (3 to 3000 μg/mL) was verified in second-order branches of the mesenteric artery (SOBMA) pre-contracted by KCl and U46619. To study the mechanism of action, the influence of several inhibitors (TEA, 4-AP, Glibenclamide, Atropine, L-NAME, ODQ and indomethacin) on the vasodilator effect of EOAz was evaluated. Some protocols were also performed aiming to study the effect of EOAz on Ca2+ influx and release from intracellular storage. Furthermore, the binding energy of the main constituents with calcium channels were evaluated by molecular docking. Results showed an endothelium-independent vasorelaxant effect of EOAz on SOBMA, and only ODQ and L-NAME produced significant alteration on its pEC 50. Regarding the calcium assays, contraction reduction caused by incubation with EOAz was observed in all three protocols. Hence, our results suggest that EOAz has a vasodilator effect mediated by inhibition of Ca2+ influx and release from intracellular storage, as well as an activation of the NOS/sGC pathway. [Display omitted] • Essential oil of Alpinia zerumbet has a vasodilator effect on the second-order branch of the mesenteric artery. • Its mechanism probably involves blocking of calcium mobilization. • Terpinen-4-ol showed good binding energy with the three calcium channels assessed by docking (VGCC, RyR and IP3R). • Terpinen-4-ol exhibited the same binding site of caffein in the ryanodine receptor with excellent binding energy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0367326X
Volume :
169
Database :
Academic Search Index
Journal :
Fitoterapia
Publication Type :
Academic Journal
Accession number :
169969152
Full Text :
https://doi.org/10.1016/j.fitote.2023.105623