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Protective and therapeutic effects of dexpanthenol on isoproterenol-induced cardiac damage in rats

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dc.contributor.author Kalkan, Ferhat
dc.contributor.author Parlakpinar, Hakan
dc.contributor.author Disli, Olcay M.
dc.contributor.author Tanriverdi, Lokman H.
dc.contributor.author Ozhan, Onural
dc.contributor.author Polat, Alaaddin
dc.contributor.author Cetin, Asli
dc.contributor.author Vardi, Nigar
dc.contributor.author Otlu, Yilmaz O.
dc.contributor.author Acet, Ahmet
dc.date.accessioned 2019-07-24T12:55:53Z
dc.date.available 2019-07-24T12:55:53Z
dc.date.issued 2018
dc.identifier.citation Kalkan, F. Parlakpinar, H. Disli, OM. Tanriverdi, LH. Ozhan, O. Polat, A. Cetin, A. Vardi, N. Otlu, YO. Acet, A. (2018). Protective and therapeutic effects of dexpanthenol on isoproterenol-induced cardiac damage in rats. Cilt:119 Sayı:9, 7479-7489 ss. tr_TR
dc.identifier.uri http://hdl.handle.net/11616/12912
dc.description.abstract The purpose of the study was to explore the protective and therapeutic effects of dexpanthenol (DEX) on isoproterenol (ISO)-induced cardiac damage. Forty rats were distributed into four groups: group I (Control); group II (ISO); ISO (150mg/kg/day) was given to rats once a day for 2 consecutive days with an interval of 24h; group III (DEX+ISO): DEX (250mg/kg) was applied 30min before the first ISO administration and continued in the next two days after second ISO administration; group IV (ISO+DEX): After the ISO treatment at 1st and 2nd days, DEX was given at 3rd and 4th days. Rats were monitored for mean arterial blood pressure (BP), heart rate, oxygen saturation (%SO2), and electrocardiography (ECG). Heart tissue levels of malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX), reduced glutathione (GSH), total oxidant status (TOS); total antioxidant capacity (TAC), oxidative stress index (OSI), and caspase-3 were determined. BP and SO2 values indicated a significant decrease in the ISO group. Also, T wave negativity was observed in 6 of 10 rats, SOD, CAT, and GPX levels were significantly lower in ISO group than control group. ISO administration increased TOS and OSI levels, whereas DEX treatment significantly reduced these parameters. Also, ISO-induced morphological alterations such as disorganization of cardiomyocytes, loss of myofibrils and cytoplasmic vacuolization whereas these histological damages were significantly decreased in ISO+DEX and DEX+ISO groups when compared to the ISO group. This study implies the cardioprotective effects of DEX on ISO-induced cardiotoxicity. tr_TR
dc.language.iso eng tr_TR
dc.publisher WILEY, 111 RIVER ST, HOBOKEN 07030-5774, NJ USA tr_TR
dc.relation.isversionof 10.1002/jcb.27058 tr_TR
dc.rights info:eu-repo/semantics/restrictedAccess tr_TR
dc.subject cardiotoxicity tr_TR
dc.subject dexpanthenol tr_TR
dc.subject heart tr_TR
dc.subject isoproterenol tr_TR
dc.subject oxidative stress tr_TR
dc.title Protective and therapeutic effects of dexpanthenol on isoproterenol-induced cardiac damage in rats tr_TR
dc.type article tr_TR
dc.relation.journal Journal of cellular bıochemıstry tr_TR
dc.contributor.department İnönü Üniversitesi tr_TR
dc.identifier.volume 119 tr_TR
dc.identifier.issue 9 tr_TR
dc.identifier.startpage 7479 tr_TR
dc.identifier.endpage 7489 tr_TR


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