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dc.contributor.authorAndalib, S
dc.contributor.authorShayanfar, A
dc.contributor.authorKhorrami, A
dc.contributor.authorMaleki-Dijazi, N
dc.contributor.authorGarjani, A
dc.date.accessioned2018-08-26T08:36:39Z
dc.date.available2018-08-26T08:36:39Z
dc.date.issued2014
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52766
dc.description.abstractThe present study was aimed to study the effects of different doses of atorvastatin on Co Q10 content in the myocardium tissue in rats. A subcutaneous injection of isoproterenol (5 mg/kg/day) for 10 days was used for the induction of heart failure. Rats were randomly assigned to control, treatment with atorvastatin (5, 10, 20 mg/kg/day) and treatment with atorvastatin plus coenzyme Q10 (10 mg/kg/day). Coenzyme Q10 content of myocardium was measured using HPLC method with UV detector after hemodynamic parameters measurements. The malondialdehyde (MDA) content of the myocardium was evaluated in order to determine coenzyme Q10 antioxidative effect. A high dose of atorvastatin (20 mg/kg/day) was significantly reduced the myocardium content of coenzyme Q10 as compared with isoproterenol treated group (p<0.001). Compared with atorvastatin alone treated animals, co-administration of coenzyme Q10 with atorvastatin was improved the level of coenzyme Q10 in the myocardium (p<0.05, p<0.001). Increasing the dose of atorvastatin also led to increase in MDA content of the myocardium (p<0.01). Serum lipid profile showed no changes in atorvastatin treated groups. The results of this study demonstrate that high doses of atorvastatin reduce coenzyme Q10 content of the myocardium and increase lipid peroxidation in myocardium which is reversed by coenzyme Q10 co-administration. é Georg Thieme Verlag KG Stuttgart.
dc.language.isoEnglish
dc.relation.ispartofDrug Research
dc.subjectatorvastatin
dc.subjectcholesterol
dc.subjecthigh density lipoprotein
dc.subjectisoprenaline
dc.subjectlipid
dc.subjectlow density lipoprotein
dc.subjectmalonaldehyde
dc.subjecttriacylglycerol
dc.subjectubidecarenone
dc.subjectantioxidant
dc.subjectatorvastatin
dc.subjectheptanoic acid derivative
dc.subjectisoprenaline
dc.subjectlipid
dc.subjectmalonaldehyde
dc.subjectpyrrole derivative
dc.subjectubidecarenone
dc.subjectubiquinone
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantioxidant activity
dc.subjectarticle
dc.subjectcontrolled study
dc.subjectdose response
dc.subjectdrug effect
dc.subjectheart failure
dc.subjectheart left ventricle dp-dt
dc.subjectheart left ventricle enddiastolic pressure
dc.subjectheart muscle
dc.subjecthemodynamic parameters
dc.subjecthigh performance liquid chromatography
dc.subjectisoproterenol induced heart failure
dc.subjectlipid blood level
dc.subjectlipid peroxidation
dc.subjectmale
dc.subjectnonhuman
dc.subjectrat
dc.subjectanalogs and derivatives
dc.subjectanimal
dc.subjectblood
dc.subjectchemically induced
dc.subjectdrug effects
dc.subjectheart failure
dc.subjectmetabolism
dc.subjectWistar rat
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectHeart Failure
dc.subjectHeptanoic Acids
dc.subjectIsoproterenol
dc.subjectLipid Peroxidation
dc.subjectLipids
dc.subjectMale
dc.subjectMalondialdehyde
dc.subjectMyocardium
dc.subjectPyrroles
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectUbiquinone
dc.titleAtorvastatin reduces the myocardial content of coenzyme Q10 in isoproterenol-induced heart failure in rats
dc.typeConference Paper
dc.citation.volume64
dc.citation.issue5
dc.citation.spage246
dc.citation.epage250
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1055/s-0033-1357178


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