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dc.contributor.authorTaziki, S
dc.contributor.authorSattari, MR
dc.contributor.authorDastmalchi, S
dc.contributor.authorEghbal, MA
dc.date.accessioned2018-08-26T07:42:08Z
dc.date.available2018-08-26T07:42:08Z
dc.date.issued2015
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/47748
dc.description.abstractPurpose: Amitriptyline, one of the commonly used tricyclic antidepressants, caused rare but severe hepatotoxicity in patients who received it continuously. Previous findings showed that the intermediate metabolites of amitriptyline produced by CYP450 are involved in hepatic injury. Melatonin is an antiaging and antioxidant hormone synthesized from pineal gland. The aim of present study was to evaluate the protective role of melatonin in an in vitro model of isolated rat hepatocytes. Methods: Markers such as cell viability, reactive oxygen species formation, lipid peroxidation, mitochondrial membrane potential, and hepatocytes glutathione content were evaluated every 60 minutes for 180 minutes. Results: Present results indicated that administration of 1mM of melatonin effectively reduced the cell death, ROS formation and lipid peroxidation, mitochondrial membrane potential collapse, and reduced cellular glutathione content caused by amitriptyline. Conclusion: Our results indicated that melatonin is an effective antioxidant in preventing amitriptyline-induced hepatotoxicity. We recommend further in vivo animal and clinical trial studies on the hepatoprotective effects of melatonin in patients receiving amitriptyline.
dc.language.isoEnglish
dc.relation.ispartofADVANCED PHARMACEUTICAL BULLETIN
dc.subjectAmitriptyline
dc.subjectMelatonin
dc.subjectOxidative stress
dc.subjectHepatocytes
dc.subjectMitochondrial membrane potential
dc.subjectGSH
dc.titleCytoprotective Effects of Melatonin Against Amitriptyline-Induced Toxicity in Isolated Rat Hepatocytes
dc.typeArticle
dc.citation.volume5
dc.citation.issue3
dc.citation.spage329
dc.citation.epage334
dc.citation.indexWeb of science


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