Perillyl Alcohol Promotes Relaxation in Human Umbilical Artery.

Perillyl alcohol human umbilical artery serotoninergic pathway vasorelaxation.

Journal

Current medicinal chemistry
ISSN: 1875-533X
Titre abrégé: Curr Med Chem
Pays: United Arab Emirates
ID NLM: 9440157

Informations de publication

Date de publication:
08 Jan 2024
Historique:
received: 28 06 2023
revised: 11 10 2023
accepted: 24 10 2023
medline: 11 1 2024
pubmed: 11 1 2024
entrez: 11 1 2024
Statut: aheadofprint

Résumé

Perillyl alcohol (POH) is a monoterpenoid found in plant essential oils and has been shown to relax murine vessels, but its effect on human vessels remains poorly studied. The study aimed to characterize the effect of POH on human umbilical arteries (HUA). Rings of HUA were obtained from uncomplicated patients and suspended in an organ bath for isometric recording. The vasorelaxant effect of POH in HUA was evaluated on basal tone and electromechanical or pharmacomechanical contractions, and possible mechanisms of action were also investigated. POH (1-1000 μM) altered the basal tone of HUA and completely relaxed HUA rings precontracted with KCl (60 mM) or 5-HT (10 μM), obtaining greater potency in the pharmacomechanical pathway (EC50 110.1 μM), suggesting a complex interference in the mobilization of extra- and intracellular Ca2+. POH (1000 μM) inhibited contractions induced by BaCl2 (0.1-30 mM) in a similar way to nifedipine (10 μM), indicating a possible blockade of L-type VOCC. In the presence of potassium channel blockers, tetraethylammonium (1 mM), 4-aminopyridine (1 mM), or glibenclamide (10 μM), an increase in the EC50 value of the POH was observed, suggesting a modulation of the activity of BKCa, KV, and KATP channels. The data from this study suggest that POH modulates Ca2+ and K+ ion channels to induce a relaxant response in HUA.

Sections du résumé

BACKGROUND BACKGROUND
Perillyl alcohol (POH) is a monoterpenoid found in plant essential oils and has been shown to relax murine vessels, but its effect on human vessels remains poorly studied.
OBJECTIVE OBJECTIVE
The study aimed to characterize the effect of POH on human umbilical arteries (HUA).
METHODS METHODS
Rings of HUA were obtained from uncomplicated patients and suspended in an organ bath for isometric recording. The vasorelaxant effect of POH in HUA was evaluated on basal tone and electromechanical or pharmacomechanical contractions, and possible mechanisms of action were also investigated.
RESULTS RESULTS
POH (1-1000 μM) altered the basal tone of HUA and completely relaxed HUA rings precontracted with KCl (60 mM) or 5-HT (10 μM), obtaining greater potency in the pharmacomechanical pathway (EC50 110.1 μM), suggesting a complex interference in the mobilization of extra- and intracellular Ca2+. POH (1000 μM) inhibited contractions induced by BaCl2 (0.1-30 mM) in a similar way to nifedipine (10 μM), indicating a possible blockade of L-type VOCC. In the presence of potassium channel blockers, tetraethylammonium (1 mM), 4-aminopyridine (1 mM), or glibenclamide (10 μM), an increase in the EC50 value of the POH was observed, suggesting a modulation of the activity of BKCa, KV, and KATP channels.
CONCLUSION CONCLUSIONS
The data from this study suggest that POH modulates Ca2+ and K+ ion channels to induce a relaxant response in HUA.

Identifiants

pubmed: 38204229
pii: CMC-EPUB-137092
doi: 10.2174/0109298673269428231204064101
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Carla Mikevely Sena Bastos (CM)

Biological Chemistry Department, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.
Biological Sciences Department, Physiopharmacology of Excitable Cells Laboratory, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.

Luis Pereira de Morais (L)

Biological Sciences Department, Physiopharmacology of Excitable Cells Laboratory, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.

Andressa de Alencar Silva (AA)

Biological Sciences Department, Physiopharmacology of Excitable Cells Laboratory, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.

Débora de Menezes Dantas (D)

Biological Chemistry Department, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.

Paulo Ricardo Batista (PR)

Biological Chemistry Department, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.
Biological Sciences Department, Physiopharmacology of Excitable Cells Laboratory, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.

Maria Franciele Lima Gomes (MF)

Biological Sciences Department, Physiopharmacology of Excitable Cells Laboratory, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.

Gyllyandeson Araújo Delmondes (G)

Universidade Regional do Cariri Quimica Biologica Crato Brazil.

Irwin Rose Alencar de Menezes (IR)

Biological Chemistry Department, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.

Renata Evaristo Rodrigues da Silva (RE)

Biological Chemistry Department, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.
Biological Sciences Department, Physiopharmacology of Excitable Cells Laboratory, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.

Roseli Barbosa (R)

Biological Chemistry Department, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.
Biological Sciences Department, Physiopharmacology of Excitable Cells Laboratory, Pimenta Campus, Regional University of Cariri, Crato 63105-000, Ceará, Brazil.

Classifications MeSH