2018, Cilt 16, Sayı 1, Sayfa(lar) 025-031 |
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Biochemical Markers in Early Period Doxorubicin-Fluoxetine Cardiotoxicity Doksorubisin-fluoksetin kardiyotoksisite |
Gül Özbey1, Selvinaz Dalaklıoğlu1, Sebahat Özdem2, Gülbahar Uzun2, Esin Tatlı1, Nuray Erin1 |
1Akdeniz Üniversitesi Tıp Fakültesi, Farmakoloji Anabilim Dalı, Antalya, Türkiye 2Akdeniz Üniversitesi Tıp Fakültesi, Biyokimya Anabilim Dalı, Antalya, Türkiye |
Keywords: Anthracyclines; antidepressant agents; adverse effects |
Aim: Doxorubicin (DOXO) is a highly effective and extensively prescribed anticancer antracycline drug,
however, its use is limited by multidrug resistance and dose-dependent cumulative cardiotoxicity.
Administration of DOXO with widely used antidepressan fluoxetine (FLU) is one of the treatment
strategies for multidrug resistance. In this study, we aimed the investigation of FLU-DOXO combination
on biochemical cardiotoxicity markers.
Material and Method: Balb-c mice divided 4 group and treated 6 weeks: (1) control (serum
physiologic), (2) FLU (0.5 mg/kg/day), (3) DOXO (cumulative dose 12 mg/kg), (4) FLU (0.5 mg/kg/day) ve
DOXO (cumulative dose 12 mg/kg).
Results: Regarding to our results, FLU-DOXO combination increased serum high sensitivity Troponin T
(hsTnT) levels. While DOXO treatment increased serum aspartate aminotransferase (AST) and cardiac
total oxidant capacity (TOS), serum alanine aminotransferase (ALT), lactate dehydrogenase (LDH) and
creatine kinase-MB (CK-MB) levels were unchanged.
Conclusion: Administration of DOXO with FLU may cause early stage cardiotoxicity which is determined
by hsTnT.
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