Cytotoxicity and antimicrobial activity of isolated compounds from Monsonia angustifolia and Dodonaea angustifolia.


Journal

Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310

Informations de publication

Date de publication:
30 Jan 2023
Historique:
received: 26 11 2021
revised: 17 02 2022
accepted: 02 03 2022
pubmed: 1 4 2022
medline: 9 11 2022
entrez: 31 3 2022
Statut: ppublish

Résumé

Monsonia angustifolia is traditionally used to treat anthrax, heartburn, diarrhea, eye infections and hemorrhoids. Dodonaea angustifolia is frequently used as a treatment for dental pain, microbial infections and jungle fever. The two plant species were selected due to the presence of secondary metabolites such as coumarins, flavonoids, terpenoids, saponins and polyphenolics from the crude extracts, which exhibit pharmacological significance. The pure isolated compounds from the crude extracts are known for their diverse structures and interesting pharmacophores. To isolate and identify antibacterial and antifungal chemical constituents from Monsonia angustifolia and Dodonaea angustifolia plant extracts and evaluate the cytotoxicity of pure compounds from the crude extracts. Extractives from M. angustifolia and D. angustifolia plants were isolated using chromatographic techniques and structures were elucidated based on NMR, IR and MS spectroscopic techniques. A microplate serial dilution method was used to evaluate the antibacterial activity of extracts and pure compounds against Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa and antifungal activity against Candida albicans and Cryptococcus neoformans. The cytotoxicity was determined using the 3-(4, 5-dimethylthiazol)-2, 5-diphenyl tetrazolium bromide (MTT) assay. The dichloromethane, ethyl acetate and methanol crude extracts from the plants exhibited significant inhibition of microbial growth. The phytochemical investigation of these active crude extracts led to the isolation of five pure active compounds, 5-methoxyjusticidin A (1), cis-phytyl diterpenoidal fatty acid ester (2), stigmasterol (3), β-sitosterol (4) and 5-hydroxy-7,4'-dimethoxyflavone (5). Stigmasterol (3) showed good antifungal activity against Cryptococcus neoformans with a minimum inhibition concentration (MIC) of 25 μg/mL and Candida albicans (MIC = 50 μg/mL). Compounds (1-5) isolated from Monsonia angustifolia and Dodonaea angustifolia showed antibacterial and antifungal activities and were non-toxic against Madin-Darby canine kidney (MDCK) cells and VERO monkey kidney (VERO) cells.

Identifiants

pubmed: 35358625
pii: S0378-8741(22)00208-2
doi: 10.1016/j.jep.2022.115170
pii:
doi:

Substances chimiques

Antifungal Agents 0
Stigmasterol 99WUK5D0Y8
Plant Extracts 0
Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

115170

Informations de copyright

Copyright © 2022. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest Authors declare no competing interests.

Auteurs

Zenande K S Mcotshana (ZKS)

Department of Chemistry, Tshwane University of Technology, Private Bag X680, Arcadia, 0001, South Africa.

Lyndy J McGaw (LJ)

Phytomedicine Programme, Department of Paraclinical Sciences, University of Pretoria, Private Bag X04, Onderstepoort, 0110, South Africa.

Douglas Kemboi (D)

Department of Chemistry, Tshwane University of Technology, Private Bag X680, Arcadia, 0001, South Africa.

Gerda Fouche (G)

Department of Chemistry, University of Pretoria, Private Bag X20, Hatfield, 0028, South Africa.

Ibukun M Famuyide (IM)

Phytomedicine Programme, Department of Paraclinical Sciences, University of Pretoria, Private Bag X04, Onderstepoort, 0110, South Africa.

Rui W M Krause (RWM)

Department of Chemistry, Rhodes University, Makhanda, 6140, South Africa.

Xavier Siwe-Noundou (X)

Department of Pharmaceutical Sciences, Sefako Makgatho Health Sciences University, Pretoria, 0204, South Africa.

Vuyelwa Jacqueline Tembu (VJ)

Department of Chemistry, Tshwane University of Technology, Private Bag X680, Arcadia, 0001, South Africa. Electronic address: Tembuvj@tut.ac.za.

Articles similaires

Vancomycin-associated DRESS demonstrates delay in AST abnormalities.

Ahmed Hussein, Kateri L Schoettinger, Jourdan Hydol-Smith et al.
1.00
Humans Drug Hypersensitivity Syndrome Vancomycin Female Male
Humans Arthroplasty, Replacement, Elbow Prosthesis-Related Infections Debridement Anti-Bacterial Agents
Vancomycin Polyesters Anti-Bacterial Agents Models, Theoretical Drug Liberation
Biofilms Candida albicans Quorum Sensing Candida glabrata Menthol

Classifications MeSH