PMID- 30067069 OWN - NLM STAT- MEDLINE DCOM- 20181218 LR - 20181218 IS - 1205-7541 (Electronic) IS - 0008-4212 (Linking) VI - 96 IP - 10 DP - 2018 Oct TI - Efficiency of atorvastatin and simvastatin in improving cardiac function during the different degrees of hyperhomocysteinemia. PG - 1040-1049 LID - 10.1139/cjpp-2018-0102 [doi] AB - The aim of this study was to assess the impact of atorvastatin and simvastatin on myocardial contractility during the different degrees of hyperhomocysteinemia (HHcy) in rats. Study was conducted on adult male Wistar albino rats (n = 90; 4 weeks old; 100 +/- 15 g body mass) in which HHcy was achieved by dietary manipulation. Animals were exposed to pharmacology treatment with atorvastatin in dose of 3 mg/kg per day i.p. or simvastatin in dose of 5 mg/kg per day i.p. at the same time every day, according to equivalent therapeutic doses of these statins (10 mg atorvastatin = 20 mg simvastatin). After the dietary manipulation and pharmacological treatment and confirmation of HHcy, all animals were sacrificed, hearts were isolated, and cardiac function was tested according to the Langendorff technique. Size of recovery of maximum rate of left ventricular development (dp/dt(max)), minimum rate of left ventricular development (dp/dt(min)), systolic left ventricular development, diastolic left ventricular development, heart rate, and coronary flow at the 40, 60, 80, 100, and 120 cmH(2)O coronary perfusion pressure were measured in state of physiological condition (homocysteine less than 15 mumol/L), mild HHcy, and moderate HHcy. Atorvastatin treatment significantly attenuated homocysteine-induced impairment of myocyte contractility and dominantly decreased dp/dt(max), dp/dt(min), and heart rate and induced greater changes in systolic left ventricular development compared with simvastatin. Treatment with atorvastatin seems able to revert systolic abnormalities and improve contractility during the different degrees of HHcy. FAU - Nikolic Turnic, Tamara R AU - Nikolic Turnic TR AD - a Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia. FAU - Jakovljevic, Vladimir Lj AU - Jakovljevic VL AD - b Department of Physiology, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia. AD - c Department of Human Pathology, IM Sechenov 1st Moscow State Medical University, Moscow, Russian Federation. FAU - Djuric, Dragan M AU - Djuric DM AD - d Institute of Medical Physiology "Richard Burian", School of Medicine, University of Belgrade, Belgrade, Serbia. FAU - Jeremic, Nevena S AU - Jeremic NS AD - a Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia. FAU - Jeremic, Jovana N AU - Jeremic JN AD - a Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia. FAU - Milosavljevic, Isidora M AU - Milosavljevic IM AD - a Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia. FAU - Srejovic, Ivan M AU - Srejovic IM AD - b Department of Physiology, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia. FAU - Selakovic, Dragica V AU - Selakovic DV AD - b Department of Physiology, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia. FAU - Zivkovic, Vladimir I AU - Zivkovic VI AD - b Department of Physiology, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia. LA - eng PT - Journal Article DEP - 20180801 PL - Canada TA - Can J Physiol Pharmacol JT - Canadian journal of physiology and pharmacology JID - 0372712 RN - 0LVT1QZ0BA (Homocysteine) RN - A0JWA85V8F (Atorvastatin) RN - AGG2FN16EV (Simvastatin) SB - IM MH - Animals MH - Atorvastatin/*pharmacology MH - Heart/*drug effects/*physiopathology MH - Homocysteine/metabolism MH - Hyperhomocysteinemia/metabolism/*physiopathology MH - Male MH - Rats MH - Rats, Wistar MH - Recovery of Function/drug effects MH - Simvastatin/*pharmacology OTO - NOTNLM OT - cardiac function OT - fonction cardiaque OT - hydroxymethyl glutaryl coenzyme A reductase inhibitors OT - hyperhomocysteinemia OT - hyperhomocysteinemie OT - inhibiteurs de l'hydroxymethyl glutaryl coenzyme A reductase OT - rat EDAT- 2018/08/02 06:00 MHDA- 2018/12/19 06:00 CRDT- 2018/08/02 06:00 PHST- 2018/08/02 06:00 [pubmed] PHST- 2018/12/19 06:00 [medline] PHST- 2018/08/02 06:00 [entrez] AID - 10.1139/cjpp-2018-0102 [doi] PST - ppublish SO - Can J Physiol Pharmacol. 2018 Oct;96(10):1040-1049. doi: 10.1139/cjpp-2018-0102. Epub 2018 Aug 1.