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| dc.contributor.author | Mohamad H.E. | |
| dc.contributor.author | Askar M.E. | |
| dc.contributor.author | Hafez M.M. | |
| dc.contributor.other | Department of Biochemistry | |
| dc.contributor.other | Faculty of Pharmacy | |
| dc.contributor.other | Zagazig University | |
| dc.contributor.other | Zagazig | |
| dc.contributor.other | Egypt; Department of Biochemistry | |
| dc.contributor.other | Faculty of Pharmacy | |
| dc.contributor.other | October for Modern Science and Arts University (MSA) | |
| dc.contributor.other | Egypt | |
| dc.date.accessioned | 2020-01-25T19:58:31Z | |
| dc.date.available | 2020-01-25T19:58:31Z | |
| dc.date.issued | 2011 | |
| dc.identifier.issn | 17585996 | |
| dc.identifier.other | https://doi.org/10.1186/1758-5996-3-4 | |
| dc.identifier.other | PubMed ID : | |
| dc.identifier.uri | https://t.ly/rx8Wv | |
| dc.description | Scopus | |
| dc.description.abstract | Background: Diabetes mellitus (DM) and hypertension (HTN) are accused of being responsible for the development of the cardiac fibrosis due to severe cardiomyopathy. Methods. Blood glucose (BG) test was carried out, lipid concentrations, tumor necrosis factor alpha (TNF-?), transforming growth factor beta (TGF-?), matrix metalloproteinase (MMP-2), collagen-I and collagen-III were measured in male Albino rats weighing 179-219 g. The rats were divided into five groups, kept on either control diet or high fat diet (HFD), and simultaneously treated with rosiglitazone (PPAR-gamma) only for one group with 3 mg/kg/day via oral route for 30 days, and with rosiglitazone and felodipine combination for another group with 3 mg/kg/day and 5 mg/kg/day, respectively via oral route for 30 days. Results: Diabetic hypertensive (DH) rats which fed on a HFD, injected with streptozotocin (STZ) (i.p.) and obstruction for its right kidney was occurred develop hyperglycemia, hypertension, cardiac fibrosis, hypertriglyceridemia, hypercholesterolemia, increased TNF-?, increased TGF-?, decreased MMP-2, increased collagen-I and increased collagen-III, when compared to rats fed on control diet. Treating the DH rats with rosiglitazone only causes a significant decrease for BG levels by 52.79%, triglycerides (TGs) by 24.05%, total cholesterol (T-Chol) by 30.23%, low density lipoprotein cholesterol (LDL-C) by 40.53%, TNF-? by 20.81%, TGF-? by 46.54%, collagen-I by 48.11% and collagen-III by 53.85% but causes a significant increase for MMP-2 by 272.73%. Moreover, Treating the DH rats with rosiglitazone and felodipine combination causes a significant decrease for BG levels by 61.08%, blood pressure (BP) by 16.78%, TGs by 23.80%, T-Chol by 33.27%, LDL-C by 45.18%, TNF-? by 22.82%, TGF-? by 49.31%, collagen-I by 64.15% and collagen-III by 53.85% but causes a significant increase for MMP-2 by 290.91%. Rosiglitazone alone failed to decrease the BP in DH rats in the current dosage and duration. Conclusion: Our results indicate that the co-existence of diabetes and hypertension could induce cardiomyopathy which could further result in cardiac fibrosis, and that combination treatment with rosiglitazone and felodipine has a great protective role against the metabolic abnormalities, meanwhile, the treatment with rosiglitazone alone has a protective role with a minimal effect against these abnormalities and has no effect on decreasing BP in these cases which may lead to coronary artery diseases (CADs) in future. � 2011 Mohamad et al; licensee BioMed Central Ltd. | en_US |
| dc.description.uri | https://www.scimagojr.com/journalsearch.php?q=19700174930&tip=sid&clean=0 | |
| dc.language.iso | English | en_US |
| dc.relation.ispartofseries | Diabetology and Metabolic Syndrome | |
| dc.relation.ispartofseries | 3 | |
| dc.subject | cholesterol | en_US |
| dc.subject | collagen type 1 | en_US |
| dc.subject | collagen type 2 | en_US |
| dc.subject | collagen type 3 | en_US |
| dc.subject | felodipine | en_US |
| dc.subject | gelatinase A | en_US |
| dc.subject | glucose | en_US |
| dc.subject | lipid | en_US |
| dc.subject | low density lipoprotein cholesterol | en_US |
| dc.subject | rosiglitazone | en_US |
| dc.subject | streptozocin | en_US |
| dc.subject | transforming growth factor beta | en_US |
| dc.subject | triacylglycerol | en_US |
| dc.subject | tumor necrosis factor alpha | en_US |
| dc.subject | animal experiment | en_US |
| dc.subject | animal model | en_US |
| dc.subject | article | en_US |
| dc.subject | controlled study | en_US |
| dc.subject | diabetes mellitus | en_US |
| dc.subject | glucose blood level | en_US |
| dc.subject | glucose tolerance test | en_US |
| dc.subject | heart muscle fibrosis | en_US |
| dc.subject | hypercholesterolemia | en_US |
| dc.subject | hyperglycemia | en_US |
| dc.subject | hypertension | en_US |
| dc.subject | hypertriglyceridemia | en_US |
| dc.subject | lipid diet | en_US |
| dc.subject | male | en_US |
| dc.subject | nonhuman | en_US |
| dc.subject | priority journal | en_US |
| dc.subject | protein function | en_US |
| dc.subject | rat | en_US |
| dc.title | Management of cardiac fibrosis in diabetic rats; The role of peroxisome proliferator activated receptor gamma (PPAR-gamma) and calcium channel blockers (CCBs) | en_US |
| dc.type | Article | en_US |
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| dcterms.source | Scopus | |
| dc.identifier.doi | https://doi.org/10.1186/1758-5996-3-4 | |
| dc.identifier.doi | PubMed ID : | |
| dc.Affiliation | October University for modern sciences and Arts (MSA) |
