Hibiscus acid from hibiscus sabdariffa (malvaceae) has a vasorelaxant effect on the rat aorta
Zheoat, Ahmed M. and Gray, Alexander I. and Igoli, John O. and Ferro, Valerie A. and Drummond, Robert M. (2019) Hibiscus acid from hibiscus sabdariffa (malvaceae) has a vasorelaxant effect on the rat aorta. Fitoterapia, 134. pp. 5-13. ISSN 0367-326X (https://doi.org/10.1016/j.fitote.2019.01.012)
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Abstract
Hibiscus sabdariffa (Malvaceae) is a plant that is widely recognised for its antihypertensive properties; however the constituent(s) responsible for this biological activity are presently unknown. The aim of this study was to identify the potential compounds that are responsible for the vasorelaxant activity of H. sabdariffa. Thereafter, the mechanisms involved in producing the vasorelaxation were investigated. The plant was extracted consecutively with hexane, ethyl acetate and methanol. The methanolic extract was subjected to bioassay-guided fractionation in order to isolate pure compounds that possessed vasorelaxant activity. The vascular effects of the pure compounds were studied on the rat aorta in vitro using myography techniques. Hibiscus acid produced a concentration-dependent relaxation of the rat aorta pre-contracted with either phenylephrine (3 μM) or KCl (60 mM), irrespective of the presence of the endothelium. When the tissue was pre-contracted with phenylephrine, the concentration required to produce 50% relaxation (IC50), was 0.09 ± 0.01 mg/ml. Hibiscus acid had no effect on the phasic contraction induced by phenylephrine in Ca2+-free physiological solution; but it did affect the component of the contraction that is due to Ca2+ influx. In parallel studies, garcinia acid, a diastereoisomer of hibiscus acid, was found to have an almost identical vasorelaxant effect. The vasorelaxant action of both compounds is most likely due to the inhibition of Ca2+ influx via voltage-dependent Ca2+ channels.
ORCID iDs
Zheoat, Ahmed M. ORCID: https://orcid.org/0000-0002-8353-6235, Gray, Alexander I., Igoli, John O., Ferro, Valerie A. ORCID: https://orcid.org/0000-0003-1967-3603 and Drummond, Robert M. ORCID: https://orcid.org/0000-0003-0003-609X;-
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Item type: Article ID code: 67033 Dates: DateEvent30 April 2019Published25 January 2019Published Online24 January 2019AcceptedSubjects: Medicine > Therapeutics. Pharmacology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 20 Feb 2019 11:46 Last modified: 18 Dec 2024 01:23 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/67033