Propolis exerts an anti-inflammatory effect on PMA-differentiated THP-1 cells via inhibition of purine nucleoside phosphorylase
Alqarni, Abdulmalik M. and Niwasabutra, Kanidta and Sahlan, Muhamad and Fearnley, Hugo and Fearnley, James and Ferro, Valerie A. and Watson, David G. (2019) Propolis exerts an anti-inflammatory effect on PMA-differentiated THP-1 cells via inhibition of purine nucleoside phosphorylase. Metabolites, 9 (4). 75. ISSN 2218-1989 (https://doi.org/10.3390/metabo9040075)
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Abstract
Previous research has shown that propolis has immunomodulatory activity. Propolis extracts from different geographic origins were assessed for their anti-inflammatory activities by investigating their ability to alter the production of tumour necrosis factor-α (TNF-α) and the cytokines interleukin-1β (IL-1β), IL-6 and IL-10 in THP-1-derived macrophage cells co-stimulated with lipopolysaccharide (LPS). All the propolis extracts suppressed the TNF-α and IL-6 LPS-stimulated levels. Similar suppression effects were detected for IL-1β, but the release of this cytokine was synergised by propolis samples from Ghana and Indonesia when compared with LPS. Overall, the Cameroonian propolis extract (P-C) was the most active and this was evaluated for its effects on the metabolic profile of unstimulated macrophages or macrophages activated by LPS. The levels of 81 polar metabolites were identified by liquid chromatography (LC) coupled with mass spectrometry (MS) on a ZIC-pHILIC column. LPS altered the energy, amino acid and nucleotide metabolism in THP-1 cells, and interpretation of the metabolic pathways showed that P-C reversed some of the effects of LPS. Overall, the results showed that propolis extracts exert an anti-inflammatory effect by inhibition of pro-inflammatory cytokines and by metabolic reprogramming of LPS activity in macrophage cells, suggesting an immunomodulatory effect.
ORCID iDs
Alqarni, Abdulmalik M., Niwasabutra, Kanidta ORCID: https://orcid.org/0000-0001-7543-3191, Sahlan, Muhamad, Fearnley, Hugo, Fearnley, James, Ferro, Valerie A. ORCID: https://orcid.org/0000-0003-1967-3603 and Watson, David G. ORCID: https://orcid.org/0000-0003-1094-7604;-
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Item type: Article ID code: 67916 Dates: DateEvent16 April 2019Published15 April 2019AcceptedSubjects: Medicine > Therapeutics. Pharmacology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 20 May 2019 11:34 Last modified: 11 Nov 2024 12:18 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/67916