Algerian Propolis from Distinct Geographical Locations: Chemical Profiles, Antioxidant Capacity, Cytotoxicity and Inhibition of 5‐Lipoxygenase Product Biosynthesis

Author:

Ayad Ahmed Sabri1ORCID,Hébert Mathieu P. A.23,Doiron Jérémie A.23,Loucif‐Ayad Wahida4ORCID,Daas Tarek1,Smagghe Guy567ORCID,Alburaki Mohamed8ORCID,Barnett David A.29ORCID,Touaibia Mohamed3ORCID,Surette Marc E.23ORCID

Affiliation:

1. Laboratory of Applied Animal Biology Faculty of Sciences Badji Mokhtar University 2300 Annaba Algeria

2. New Brunswick Centre for Precision Medicine Moncton NB E1A 3E9 Canada

3. Department of Chemistry and Biochemistry Université de Moncton Moncton NB E1A 3E9 Canada

4. Faculty of Medicine Badji Mokhtar University 23000 Annaba Algeria

5. Ghent University 9000 Ghent Belgium

6. Institute of Entomology Guizhou University 550025 Guiyang China

7. Department of Biology Vrije Universiteit Brussel (VUB) 1050 Brussels Belgium

8. Bee Research Laboratory United States Department of Agriculture 20705 Beltsville MD United States

9. Atlantic Cancer Research Institute Moncton NB E1C 8X3 Canada

Abstract

AbstractPropolis was collected from honeybee hives in three geographically distinct Algerian climates and extracts were characterized for composition and bioactivity. Bees were identified as native subspecies using an in‐silico DraI mtDNA COI‐COII test. Over 20 compounds were identified in extracts by LC‐MS. Extracts from the Medea region were more enriched in phenolic content (302±28 mg GAE/g of dry extract) than those from Annaba and Ghardaia regions. Annaba extracts had the highest flavonoid content (1870±385 mg QCE/g of dry extract). Medea extracts presented the highest free‐radical scavenging activity (IC50=13.5 μg/mL) using the DPPH radical assay while Ghardaia extracts from the desert region were weak (IC50>100 μg/mL). Antioxidant activities measured using AAPH oxidation of linoleic acid were similar in all extracts with IC50 values ranging from 2.9 to 4.9 μg/mL. All extracts were cytotoxic (MTT assay) and proapoptotic (Annexin‐V) against human leukemia cell lines in the low μg/mL range, although the Annaba extract was less active against the Reh cell line. Extracts inhibited cellular 5‐lipoxygenase product biosynthesis with IC50 values ranging from 0.6 to 3.2 μg/mL. Overall, examined propolis extracts exhibited significant biological activity that warrant further characterization in cellular and in vivo models.

Funder

New Brunswick Innovation Foundation

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

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