ROLE OF L-, N- AND T-TYPE CALCIUM CHANNELS IN ACHIEVING MAXIMUM ANALGESIC AND MINIMUM TOXIC EFFECT OF TRAMADOL

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The aim of the study was to investigate the effects of lacidipine, amlodipine, and benidipine on the analgesic activity and toxicity of tramadol. Rats (n = 6/each group) were divided into five groups as control (CG), tramadol (TRD), lacidipine+tramadol (LTRD), amlodipine+tramadol (ATRD), and benidipine+tramadol (BTRD). Tramadol was administered once at a dose of 50 mg/kg and lacidipine, amlodipin, benidipin were administered at a dose of 4 mg/kg orally, once a day for 10 days. After the animals were sacrificed, malondialdehyde (MDA) and total glutathione (tGSH) levels were measured in brain, heart, liver, and kidney tissues. Troponin I (Tp I), alanine aminotransferase (ALT), aspartate aminotransferase (AST), blood urea nitrogen (BUN), and creatinine levels were determined in serum. Paw pain thresholds were measured one hour before and after drug administration. The analgesic effect of tramadol was increased the most by benidipine, while amlodipine and lacidipine increased it equally. Lacidipine failed to suppress MDA increase and tGSH decrease in brain tissue. Benidipine suppressed MDA increase and tGSH decrease in brain tissue better than amlodipine. All three drugs suppressed cardiac tissue oxidative stress and the release of TP I into the circulation. Lacidipine and amlodipine could not prevent tramadol-induced oxidative stress in liver and kidney tissues, whereas benidipine prevented excessive MDA increase and tGSH decrease. Benidipine significantly suppressed the increase of ALT, AST, BUN, and creatinine. Analgesic activity was 35.1% in TRD, 43.7% in LTRD, 50.4% in ATRD, and 67.5% in BTRD. Study results show that benidipine and tramadol co-treatment is better than co-treatment with lacidipine or amlodipine in achieving minimal toxic effects and maximum analgesia. © 2024 by Polish Pharmaceutical Society. This is an open-access article under the CC BY NC license (https://creativecommons.org/licenses/by-nc/4.0/).

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/11817Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.32383/appdr/179230Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorYi̇Lmaz, Mehmet
dc.contributor.authorSuleyman, Bahadi̇R
dc.contributor.authorMammadov, Renad
dc.contributor.authorAltuner, Durdu
dc.contributor.authorCoban, Taha Abdulkadi̇R
dc.contributor.authorBulut, Seval
dc.contributor.authorCoskun, Resi̇T
dc.contributor.authorSuleyman, Hali̇S
dc.date.accessioned2026-10-18T20:26:48.660360996Z
dc.date.available2026-10-18T20:26:48.660360996Z
dc.date.issued2024
dc.description.abstractThe aim of the study was to investigate the effects of lacidipine, amlodipine, and benidipine on the analgesic activity and toxicity of tramadol. Rats (n = 6/each group) were divided into five groups as control (CG), tramadol (TRD), lacidipine+tramadol (LTRD), amlodipine+tramadol (ATRD), and benidipine+tramadol (BTRD). Tramadol was administered once at a dose of 50 mg/kg and lacidipine, amlodipin, benidipin were administered at a dose of 4 mg/kg orally, once a day for 10 days. After the animals were sacrificed, malondialdehyde (MDA) and total glutathione (tGSH) levels were measured in brain, heart, liver, and kidney tissues. Troponin I (Tp I), alanine aminotransferase (ALT), aspartate aminotransferase (AST), blood urea nitrogen (BUN), and creatinine levels were determined in serum. Paw pain thresholds were measured one hour before and after drug administration. The analgesic effect of tramadol was increased the most by benidipine, while amlodipine and lacidipine increased it equally. Lacidipine failed to suppress MDA increase and tGSH decrease in brain tissue. Benidipine suppressed MDA increase and tGSH decrease in brain tissue better than amlodipine. All three drugs suppressed cardiac tissue oxidative stress and the release of TP I into the circulation. Lacidipine and amlodipine could not prevent tramadol-induced oxidative stress in liver and kidney tissues, whereas benidipine prevented excessive MDA increase and tGSH decrease. Benidipine significantly suppressed the increase of ALT, AST, BUN, and creatinine. Analgesic activity was 35.1% in TRD, 43.7% in LTRD, 50.4% in ATRD, and 67.5% in BTRD. Study results show that benidipine and tramadol co-treatment is better than co-treatment with lacidipine or amlodipine in achieving minimal toxic effects and maximum analgesia. © 2024 by Polish Pharmaceutical Society. This is an open-access article under the CC BY NC license (https://creativecommons.org/licenses/by-nc/4.0/).
dc.identifier.doi10.32383/appdr/179230
dc.identifier.eissn2353-5288
dc.identifier.endpage143
dc.identifier.issn0001-6837
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85190887749
dc.identifier.startpage135
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11817
dc.identifier.volume81
dc.identifier.wosWOS:001243807500010
dc.language.isoen
dc.publisherPolish Pharmaceutical Society
dc.relation.ispartofActa Poloniae Pharmaceutica - Drug Research
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectamlodipin
dc.subjectanalgesic activity
dc.subjectbenidipin
dc.subjectlacidipin
dc.subjecttoxicity
dc.subjecttramadol
dc.subjectalanine aminotransferase
dc.subjectamlodipine
dc.subjectaspartate aminotransferase
dc.subjectbenidipine
dc.subjectcalcium channel L type
dc.subjectcalcium channel N type
dc.subjectcalcium channel T type
dc.subjectcreatinine
dc.subjectglutathione
dc.subjectlacidipine
dc.subjectmalonaldehyde
dc.subjectnitrogen
dc.subjectreduced nicotinamide adenine dinucleotide phosphate
dc.subjectthiopental
dc.subjecttroponin I
dc.subjecturea
dc.subjectadult
dc.subjectalanine aminotransferase blood level
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectaspartate aminotransferase blood level
dc.subjectbrain tissue
dc.titleROLE OF L-, N- AND T-TYPE CALCIUM CHANNELS IN ACHIEVING MAXIMUM ANALGESIC AND MINIMUM TOXIC EFFECT OF TRAMADOL
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus0
rdl.citation.wos0
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)