In Vivo Diuretic Activity and Anti-Hypertensive Potential of Hibiscus sabdariffa Extract by Inhibition of Angiotensin-Converting Enzyme and Hypertension Precursor Enzymes

Author:

Sanou Abdoudramane1ORCID,Konaté Kiessoun12,Belemnaba Lazare3ORCID,Sama Hemayoro1ORCID,Kaboré Kabakdé1ORCID,Dakuyo Roger1ORCID,Nitiéma Mathieu3,Dicko Mamoudou Hama1ORCID

Affiliation:

1. Laboratory Biochemistry, Biotechnology, Food Technology and Nutrition, Department of Biohemistry and Microbiology, University Joseph KI-ZERBO, Ouagadougou 03 BP 7021, Burkina Faso

2. Applied Sciences and Technologies Training and Research Unit, Department of Biochemistry and Microbiology, University of Dedougou, Dedougou 09 BP 176, Burkina Faso

3. Department of Traditional Medicine and Pharmacopoeia and Pharmacy, Institute of Research in Health Sciences/National Centre for Scientific and Technological Research (MEPHATRA PH/IRSS/CNRST), Ouagadougou 03 BP 7034, Burkina Faso

Abstract

Aqueous extracts of calyx from Hibiscus sabdariffa (HS) (roselle) are highly appreciated for their nutritional and therapeutic effects, especially as anti-hypertensive substances. This study aimed to evaluate their anti-hypertensive potential through an in vitro inhibition assay of angiotensin-converting enzyme (ACE) and hypertension precursor enzymes and to assess the in vivo diuretic activity of HS. Results showed that HS extract inhibited enzymes belonging to several classes, such as α-amylase, trypsin, chymotrypsin, xanthine oxidase, lipoxygenase, and angiotensin-converting enzyme. In particular, enzymatic kinetics of ACE indicated a competitive inhibition fashion of HS extract. Furthermore, the extracts showed remarkable diuretic and natriuretic effects at doses of 50 mg/kg/bw, 100 mg/kg/b.w, and 200 mg/kg.b.w. These activities can be explained by the high content of phenolic compounds and essential amino acids. Roselle could be a potential source of nutraceuticals and anti-hypertensive bioactive compounds.

Funder

West African Biotechnology Network

Publisher

MDPI AG

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