In vitro inhibition of three different drugs used in rheumatoid arthritis treatment on human serum paraoxanase 1 enzyme activity

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We studied in vitro effects of three different drugs (ibuprofen, meloxicam and methotrexate) which are often used in rheumatoid arthritis (RA) treatment on human serum paraoxanase1 (PON1) enzyme activity. The drugs used in RA treatment decreased the in vitro PON1 activity. The inhibition mechanism of ibuprofen and methotrexate were noncompetitive whereas meloxicam was a competitive inhibitor. The IC50 values for ibuprofen, meloxicam and methotrexate were calculated to be 0.35 mM, 0.10 mM, and 0.18 mM, respectively, and the Ki constants were calculated to be 0.890 mM, 0.125 mM, and 0.260 mM, respectively. The IC50 and Ki values showed the maximum inhibition of meloxicam drugs. We propose a prediction scheme for the interaction of meloxicam with the PON1 active site because we thought that meloxicam interacts with the amino acids which are in the PON1 enzyme active site. The results we found showed that these drugs which are often used in RA treatment in vitro inhibit the activity of the enzyme with different inhibition mechanisms at low doses. © 2015 Bentham Science Publishers.

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AlanDeğerDil
dc.contributor.authorDileka, Esra
dc.contributor.authorPolat, Muhammet F.
dc.date.accessioned2026-10-18T20:29:59.331850652Z
dc.date.available2026-10-18T20:29:59.331850652Z
dc.date.issued2016
dc.description.abstractWe studied in vitro effects of three different drugs (ibuprofen, meloxicam and methotrexate) which are often used in rheumatoid arthritis (RA) treatment on human serum paraoxanase1 (PON1) enzyme activity. The drugs used in RA treatment decreased the in vitro PON1 activity. The inhibition mechanism of ibuprofen and methotrexate were noncompetitive whereas meloxicam was a competitive inhibitor. The IC50 values for ibuprofen, meloxicam and methotrexate were calculated to be 0.35 mM, 0.10 mM, and 0.18 mM, respectively, and the Ki constants were calculated to be 0.890 mM, 0.125 mM, and 0.260 mM, respectively. The IC50 and Ki values showed the maximum inhibition of meloxicam drugs. We propose a prediction scheme for the interaction of meloxicam with the PON1 active site because we thought that meloxicam interacts with the amino acids which are in the PON1 enzyme active site. The results we found showed that these drugs which are often used in RA treatment in vitro inhibit the activity of the enzyme with different inhibition mechanisms at low doses. © 2015 Bentham Science Publishers.
dc.description.sponsorshipThis research was financed by a grant from Research Fund of the Erzincan University. The authors are grateful to the Erzincan University for financial support (Project no: BAP SAG-A-140613-0037).
dc.identifier.doi10.2174/0929866522666151013130102
dc.identifier.eissn1875-5305
dc.identifier.endpage8
dc.identifier.issn0929-8665
dc.identifier.issue1
dc.identifier.pmid26458405
dc.identifier.scopus2-s2.0-84953708025
dc.identifier.startpage3
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15201
dc.identifier.volume23
dc.identifier.wosWOS:000365804900002
dc.language.isoen
dc.publisherBentham Science Publishers
dc.relation.ispartofProtein and Peptide Letters
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectIbuprofen
dc.subjectInhibition
dc.subjectMeloxicam
dc.subjectMethotrexate. paraoxonase1
dc.subjectAntirheumatic Agents
dc.subjectAryldialkylphosphatase
dc.subjectCatalytic Domain
dc.subjectDose-Response Relationship, Drug
dc.subjectHumans
dc.subjectIn Vitro Techniques
dc.subjectMethotrexate
dc.subjectThiazines
dc.subjectThiazoles
dc.subjectaryldialkylphosphatase 1
dc.subjectantirheumatic agent
dc.subjectPON1 protein, human
dc.subjectthiazine derivative
dc.subjectthiazole derivative
dc.subjectArticle
dc.subjectcompetitive inhibition
dc.subjectconcentration response
dc.subjectcontrolled study
dc.subjectdissociation constant
dc.subjectdrug effect
dc.subjectdrug interaction
dc.subjectenzyme active site
dc.subjectenzyme activity
dc.subjectenzyme blood level
dc.subjectenzyme inhibition
dc.subjecthuman
dc.titleIn vitro inhibition of three different drugs used in rheumatoid arthritis treatment on human serum paraoxanase 1 enzyme activity
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus13
rdl.citation.wos14
rdl.departmentDepartment of Biochemistry, Division of Pharmaceutical Basic Sciences, Faculty of Pharmacy, Erzincan University, 24030, Erzincan-Turkey. edilek@erzincan.edu.tr.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)