Effect of thiamine pyrophosphate on oxidative damage to the oropharyngeal, nasal and cochlear tissues induced by doxorubicin in Guinea pigs

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Doxorubicin (DOX) inhibits the enzyme tyaminpyrophosphokinase (TPK). Hence the synthesis of thiamine pyrophosphate (TPP) which is the active metabolite of thiamine stops. This leads to oxidative damage. In the literature, no studies on the protective effect of TPP against doxorubicin-induced oropharyngeal, nose and cochlear oxidative damage were found. In this study was investigated whether DOX produces oxidative stress in the oropharyngeal, nose and cochlea of animals and it examines the protective effect of TPP against DOX toxicity on these tissues. Guinea pig experimental animals were divided into groups as the controls. One group was given DOX, another group was given TPP + doxorubicin (TDOX) and the final group was the healthy group (HG). The TDOX group (n = 6) received an intraperi-toneal (ip) injection of 25 mg/kg TPP. The DOX (n = 6) and HG (n = 6) animals were given distilled water in the same way. TDOX and DOX animals were administered ip 5 mg/kg DOX one hour after the administration of TPP and distilled water once a day for seven days. At the end of this period, animals were sacri-fied with a high dose of anesthesia and the levels of malondialdehyde (MDA), myeloperoxidase (MPO), ni-tric oxide (NO), total glutathione (tGSH) and glutathione reductase (GSHRd) were determined in the removed oropharyngeal, nasal, and cochlear tissues. In addition, the TNF-α gene expression was measured. DOX was demonstrated to significantly increase the levels of MDA, MPO and NO and to reduce the levels of tGSH and GSHRd in the oropharyngeal, nasal and cochlear tissues of animals. TPP prevented the increase of the levels of MDA, MPO, NO and TNF-α with doxorubicin. TPP supressed the oxidative stress induced by DOXin the oropharyngeal, nasal and cochlear tissues. It can be suggested that TPP can be used against DOX toxicity © 2017, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.

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AlanDeğerDil
dc.contributor.authorErhan, Ertugrul
dc.contributor.authorTuran, Fatih
dc.contributor.authorTerzi, Suat
dc.contributor.authorCeliker, Metin
dc.contributor.authorMammadov, Renad
dc.contributor.authorMalkoc, Ismail
dc.contributor.authorKukula, Osman
dc.contributor.authorCankaya, Murat
dc.date.accessioned2026-10-18T20:29:36.927498127Z
dc.date.available2026-10-18T20:29:36.927498127Z
dc.date.issued2017
dc.description.abstractDoxorubicin (DOX) inhibits the enzyme tyaminpyrophosphokinase (TPK). Hence the synthesis of thiamine pyrophosphate (TPP) which is the active metabolite of thiamine stops. This leads to oxidative damage. In the literature, no studies on the protective effect of TPP against doxorubicin-induced oropharyngeal, nose and cochlear oxidative damage were found. In this study was investigated whether DOX produces oxidative stress in the oropharyngeal, nose and cochlea of animals and it examines the protective effect of TPP against DOX toxicity on these tissues. Guinea pig experimental animals were divided into groups as the controls. One group was given DOX, another group was given TPP + doxorubicin (TDOX) and the final group was the healthy group (HG). The TDOX group (n = 6) received an intraperi-toneal (ip) injection of 25 mg/kg TPP. The DOX (n = 6) and HG (n = 6) animals were given distilled water in the same way. TDOX and DOX animals were administered ip 5 mg/kg DOX one hour after the administration of TPP and distilled water once a day for seven days. At the end of this period, animals were sacri-fied with a high dose of anesthesia and the levels of malondialdehyde (MDA), myeloperoxidase (MPO), ni-tric oxide (NO), total glutathione (tGSH) and glutathione reductase (GSHRd) were determined in the removed oropharyngeal, nasal, and cochlear tissues. In addition, the TNF-α gene expression was measured. DOX was demonstrated to significantly increase the levels of MDA, MPO and NO and to reduce the levels of tGSH and GSHRd in the oropharyngeal, nasal and cochlear tissues of animals. TPP prevented the increase of the levels of MDA, MPO, NO and TNF-α with doxorubicin. TPP supressed the oxidative stress induced by DOXin the oropharyngeal, nasal and cochlear tissues. It can be suggested that TPP can be used against DOX toxicity © 2017, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.
dc.identifier.endpage1122
dc.identifier.issn0326-2383
dc.identifier.issue6
dc.identifier.scopus2-s2.0-85019858814
dc.identifier.startpage1115
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14816
dc.identifier.volume36
dc.language.isoen
dc.publisherColegio de Farmaceuticos de la Provincia de Buenos Aires
dc.relation.ispartofLatin American Journal of Pharmacy
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCochlea
dc.subjectDoxorubicin
dc.subjectOropharynx
dc.subjectOxidative stres
dc.subjectThiamine pyrophosphate
dc.subjectcocarboxylase
dc.subjectcomplementary DNA
dc.subjectglutathione
dc.subjectglutathione reductase
dc.subjectmalonaldehyde
dc.subjectmyeloperoxidase
dc.subjectnitric oxide
dc.subjecttumor necrosis factor
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectantioxidant activity
dc.subjectArticle
dc.subjectbiochemical analysis
dc.subjectcontrolled study
dc.subjectgene expression
dc.subjectguinea pig
dc.subjectmale
dc.subjectnonhuman
dc.subjectnose
dc.subjectoropharynx pain
dc.subjectoxidative stress
dc.subjectreal time polymerase chain reaction
dc.subjectRNA isolation
dc.subjectspectrophotometry
dc.titleEffect of thiamine pyrophosphate on oxidative damage to the oropharyngeal, nasal and cochlear tissues induced by doxorubicin in Guinea pigs
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus0
rdl.source.indexSCOPUS