H. Ali, A. Rahman, S. Islam, A. Mamun, Shaheda Zannah, A. Alam, A. Rahman, M. Rashid
{"title":"Combined Therapy of Pioglitazone and Atorvastatin Alleviate Diabetes in Rats More Effectively than That of Mono Therapy","authors":"H. Ali, A. Rahman, S. Islam, A. Mamun, Shaheda Zannah, A. Alam, A. Rahman, M. Rashid","doi":"10.4236/PP.2014.55060","DOIUrl":null,"url":null,"abstract":"Present research \nwas designated to investigate the hypoglycemic, hypolipidemic and antioxidant \nactivity of the combination of pioglitazone and atorvastatin on long-term \nalloxan-induced diabetes rats (AIDRs). The experiments were carried out to \ndetermine blood glucose level, lipid profile, free radial scavenging \nactivities, superoxide dismutase (SOD) and catalase in liver tissue. In \naddition, left ventricular (LV) hypertrophy and cardiomyocyte size were also \ndetermined by histological analysis. It was found that in short-term induction, \npioglitazone significantly reduced the blood glucose level without having any \nconsiderable effect on lipid profile and antioxidant enzymes (SOD and catalase) \nin rats. On the other hand, atorvastatin significantly reduced total \ncholesterol (TC), triglyceride (TG) and low density lipoprotein cholesterol \n(LDL-C) with marked increase in the level of high density lipoprotein \ncholesterol (HDL-C) and improved activity of SOD and catalase enzymes. However, \npathological changes of heart and pancreas were not observed after short-term \nexposure to alloxan in rats. Long-term diabetes induction resulted in LV \nhypertrophy and prominent shrinkage of islets of Langerhans cells. Treatment \nwith atorvastatin in combination with pioglitazone significantly reduced the LV \nhypertrophy, TC, TG and LDL level whereas they noticeably increased HDL \nlevel, DPPH (1,1-Diphenyl-2-picryl-hydrazyl) free radical scavenging activity, \nSOD and catalase activity with satisfactory recovery of Langerhans cells. The \nresult demonstrated that combination therapy was more effective than that of \nmono-therapy for preventing diabetes with cardiovascular diseases (CVD) in \nrats.","PeriodicalId":432281,"journal":{"name":"Pharmacology & Pharmacy","volume":"94 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2014-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacology & Pharmacy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4236/PP.2014.55060","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
Present research
was designated to investigate the hypoglycemic, hypolipidemic and antioxidant
activity of the combination of pioglitazone and atorvastatin on long-term
alloxan-induced diabetes rats (AIDRs). The experiments were carried out to
determine blood glucose level, lipid profile, free radial scavenging
activities, superoxide dismutase (SOD) and catalase in liver tissue. In
addition, left ventricular (LV) hypertrophy and cardiomyocyte size were also
determined by histological analysis. It was found that in short-term induction,
pioglitazone significantly reduced the blood glucose level without having any
considerable effect on lipid profile and antioxidant enzymes (SOD and catalase)
in rats. On the other hand, atorvastatin significantly reduced total
cholesterol (TC), triglyceride (TG) and low density lipoprotein cholesterol
(LDL-C) with marked increase in the level of high density lipoprotein
cholesterol (HDL-C) and improved activity of SOD and catalase enzymes. However,
pathological changes of heart and pancreas were not observed after short-term
exposure to alloxan in rats. Long-term diabetes induction resulted in LV
hypertrophy and prominent shrinkage of islets of Langerhans cells. Treatment
with atorvastatin in combination with pioglitazone significantly reduced the LV
hypertrophy, TC, TG and LDL level whereas they noticeably increased HDL
level, DPPH (1,1-Diphenyl-2-picryl-hydrazyl) free radical scavenging activity,
SOD and catalase activity with satisfactory recovery of Langerhans cells. The
result demonstrated that combination therapy was more effective than that of
mono-therapy for preventing diabetes with cardiovascular diseases (CVD) in
rats.