4.6 Article

Basic Pharmacological Characterization of EV-34, a New H2S-Releasing Ibuprofen Derivative

Journal

MOLECULES
Volume 26, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/molecules26030599

Keywords

gasotransmitter; hydrogen-sulfide; H2S-releasing-ibuprofen; thiolacetic acid; anti-inflammatory property

Funding

  1. European Union
  2. European Social Fund
  3. Higher Education Institutional Excellence Program [NKFIH-1150-6/2019]
  4. National Research, Development and Innovation Office of Hungary [NKFIH-K-124719, NKFIH-K-132870]
  5. Thematic Excellence Programme of the Ministry for Innovation and Technology in Hungary [TKP2020-IKA-04]
  6. [GINOP-2.3.2-15-2016-00043]
  7. [EFOP3.6.1-16-2016-00022]

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The newly designed H2S-releasing ibuprofen derivative EV-34 is stable under oxidative conditions, exhibits anti-inflammatory properties, and shows no cytotoxic effects.
Background: Cardioprotective effects of H2S are being suggested by numerous studies. Furthermore, H2S plays a role in relaxation of vascular smooth muscle, protects against oxidative stress, and modulates inflammation. Long-term high-dose use of NSAIDs, such as ibuprofen, have been associated with enhanced cardiovascular risk. The goal of the present work is the synthesis and basic pharmacological characterization of a newly designed H2S-releasing ibuprofen derivative. Methods: Following the synthesis of EV-34, a new H2S-releasing derivative of ibuprofen, oxidative stability assays were performed (Fenton and porphyrin assays). Furthermore, stability of the molecule was studied in rat serum and liver lysates. H2S-releasing ability of the EC-34 was studied with a hydrogen sulfide sensor. MTT (3-(4,5-dimethylthiazol 2-yl)-2,5-(diphenyltetrazolium bromide)) assay was carried out to monitor the possible cytotoxic effect of the compound. Cyclooxygenase (COX) inhibitory property of EV-34 was also evaluated. Carrageenan assay was carried out to compare the anti-inflammatory effect of EV-34 to ibuprofen in rat paws. Results: The results revealed that the molecule is stable under oxidative condition of Fenton reaction. However, EV-34 undergoes biodegradation in rat serum and liver lysates. In cell culture medium H2S is being released from EV-34. No cytotoxic effect was observed at concentrations of 10, 100, 500 mu M. The COX-1 and COX-2 inhibitory effects of the molecule are comparable to those of ibuprofen. Furthermore, based on the carrageenan assay, EV-34 exhibits the same anti-inflammatory effect to that of equimolar amount of ibuprofen (100 mg/bwkg). Conclusion: The results indicate that EV-34 is a safe H2S releasing ibuprofen derivative bearing anti-inflammatory properties.

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