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Total Phenolic and Flavonoid Content and Biological Activities of Extracts and Isolated Compounds of Cytisus villosus Pourr
- Source :
- Biomolecules, Volume 9, Issue 11
- Publication Year :
- 2019
- Publisher :
- MDPI, 2019.
-
Abstract
- The aim of this study was to evaluate the total phenolic and flavonoid content, and the in vitro antioxidant, anti-inflammatory, antibacterial, antifungal, antimalarial, cytotoxicity, and antiprotozoal activities of the Algerian plant Cytisus villosus Pourr. (Syn. Cytisus triflorus L&rsquo<br />H&eacute<br />rit.). Additionally, the radioligand displacement affinity on opioid and cannabinoid receptors was assessed for the extracts and isolated pure compounds. The hydro alcoholic extract of the aerial part of C. villosus was partitioned with chloroform (CHCl3), ethyl acetate (EtOAc), and n-butanol (n-BuOH). The phenolic content of the C. villosus extracts was evaluated using a modified Folin&ndash<br />Ciocalteau method. The total flavonoid content was measured spectrometrically using the aluminum chloride colorimetric assay. The known flavonoids genistein (1), chrysin (2), chrysin-7-O-&beta<br />d-glucopyranoside (3), and 2&Prime<br />O-&alpha<br />l-rhamnosylorientin (4) were isolated. The antioxidant activities of the extracts and isolated compounds were evaluated using 2,2-diphenyl-1-picrylhydrazyl (DDPH) and cellular antioxidant activity (CAA) assays. The plant extracts showed moderate antioxidant activity. EtOAc and n-BuOH extracts showed moderate anti-inflammatory activity through the inhibition of induced nitric oxide synthase (iNOS) with IC50 values of 48 and 90 &micro<br />g/mL, respectively. The isolated pure compounds 1 and 3 showed good inhibition of Inducible nitric oxide synthase (iNOS) with IC50 values of 9 and 20 &micro<br />g/mL, respectively. Compounds 1 and 2 exhibited lower inhibition of Nuclear Factor kappa-light-chain-enhancer of activated B cells (NF-&kappa<br />B) with IC50 values of 28 and 38 &micro<br />g/mL, respectively. Furthermore, the extracts and isolated pure compounds have been shown to exhibit low affinity for cannabinoid and opioid receptors. Finally, n-BuOH extract was a potent inhibitor of Trypanosoma brucei with IC50 value of 7.99 &micro<br />g/mL and IC90 value of 12.61 &micro<br />g/mL. The extracts and isolated compounds showed no antimicrobial, antimalarial nor antileishmanial activities. No cytotoxic effect was observed on cancer cell lines. The results highlight this species as a promising source of anti-inflammatory and antitrypanosomal agents.
- Subjects :
- Antioxidant
antioxidant
medicine.medical_treatment
Flavonoid
Cytisus villosus
Ethyl acetate
Genistein
antileishmanial
Nitric Oxide Synthase Type II
Biochemistry
Antioxidants
chemistry.chemical_compound
Mice
0302 clinical medicine
antitrypanosomal
Hydroxybenzoates
heterocyclic compounds
Chrysin
anti-inflammatory
Cytisus
chemistry.chemical_classification
0303 health sciences
antimalarial
NF-kappa B
food and beverages
Biological activity
Trypanocidal Agents
3. Good health
Enzyme Induction
Antiprotozoal
cytotoxicity
medicine.drug_class
Trypanosoma brucei brucei
Anti-inflammatory
Article
03 medical and health sciences
medicine
Animals
Molecular Biology
030304 developmental biology
Flavonoids
Chromatography
Plant Extracts
fungi
cannabinoid receptor
opioid receptor
antibacterial
RAW 264.7 Cells
chemistry
030217 neurology & neurosurgery
antifungal
Subjects
Details
- Language :
- English
- ISSN :
- 2218273X
- Volume :
- 9
- Issue :
- 11
- Database :
- OpenAIRE
- Journal :
- Biomolecules
- Accession number :
- edsair.doi.dedup.....6d711ec39263286882dfaa96baeebf8f