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Original Research Article | OPEN ACCESS

Celastrol attenuates fMLP-induced superoxide anion generation, myeloperoxidase production, and elastase release by human neutrophils

Nipapan Malisorn , Ammara Chaikan

Division of Pharmacology, Preclinical Sciences, Faculty of Medicine, Thammasat University, Pathumthani, Thailand;

For correspondence:-  Nipapan Malisorn   Email: dr.nipapan@gmail.com   Tel:+6629269716

Accepted: 19 August 2019        Published: 30 September 2019

Citation: Malisorn N, Chaikan A. Celastrol attenuates fMLP-induced superoxide anion generation, myeloperoxidase production, and elastase release by human neutrophils. Trop J Pharm Res 2019; 18(9):1805-1809 doi: 10.4314/tjpr.v18i9.3

© 2019 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the anti-inflammatory effect of celastrol via attenuation of formyl-methionyl-leucyl-phenylalanine (fMLP)-induced superoxide generation, myeloperoxidase production, and elastase release by peripheral blood neutrophils.
Methods: Cytotoxicity of celastrol on human peripheral blood neutrophils was investigated using a 2H-tetrazolium hydroxide (XTT) assay. Human neutrophils were stimulated with 100-nM fMLP; the effect of celastrol on superoxide generation was determined via ferricytochrome C reduction, the effect on myeloperoxidase production by tetramethylbenzidine oxidation, and the effect on elastase activity by Boc-Ala-ONp hydrolysis.
Results: Treatment of human neutrophils with celastrol showed dose-dependent inhibition of fMLP-induced superoxide generation, myeloperoxidase production, and elastase release with half-maximal inhibitory concentration (IC50) values of 5.9 ± 0.1, 1.9 ± 0.2, and 1.5 ± 0.1 µM, respectively.
Conclusion: These results indicate that celastrol possesses anti-inflammatory properties via attenuation of fMLP-induced superoxide generation, myeloperoxidase production, and elastase release by peripheral blood neutrophils.

Keywords: Celastrol, Anti-inflammatory, Superoxide anion generation, Myeloperoxidase, Neutrophil elastase

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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