000 03388cam a2200325 a 4500
003 EG-GiCUC
008 170308s2016 ua dh f m 000 0 eng d
040 _aEG-GiCUC
_beng
_cEG-GiCUC
041 0 _aeng
049 _aDeposite
097 _aPh.D
099 _aCai01.11.03.Ph.D.2016.Di.E
100 0 _aDina Mohamed Mekawy Rabie
245 1 0 _aEffects of administration of mesenchymal stem cells with and without PPAR-Þ agonist and Exendin-4 on mitochondrial dysfunction in diabetic cardiovascular complications in rats /
_cDina Mohamed Mekawy Rabie ; Supervised Mohamed Abdelaziz Wassef , Ola Mostafa Tork , Walaa Ibrahim Ali
246 1 5 _aتأثيرإضافه الخلايا الجذعية مع أو بدون محفزات البابار-جاما و الإكسيندين-٤ على الخلل الوظيفى للميتوكوندريا فى مضاعفات القلب لمرض البوال السكرى فى فئران التجارب
260 _aCairo :
_bDina Mohamed Mekawy Rabie ,
_c2016
300 _a204 P. :
_bcharts , facsimiles ;
_c25cm
502 _aThesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Medical Biochemistry
520 _aBackground: Diabetic cardiomyopathy (DCM) is defined as the cardiovascular damage present in diabetic patients, which is characterized by myocardial dilatation and hypertrophy, as well as a decrease in the systolic and diastolic function of the left ventricle. Therapy targeting mitochondria may provide novel ways to treat diabetes or to minimize the complications of diabetes or both. The PPAR agonists, in addition to their insulin-sensitizing properties,they have potential to affect cardiovascular disease risk in patients with type 2 diabetes .Bone marrow derived mesenchymal stem cells (MSCs) have shown great potential in cell therapy of solid organs. Exendin-4 is an analog of glucagon-like peptide-1(GLP-1). It promotes insulin gene transcription, synthesis and secretion. It inhibits the apoptosis of pancreatic Ý-cells at the gene level and promotes proliferation and regeneration. So we designed this work to evaluate the effect of MSCs, PPAR Þ agonist and Exendin-4 on diabetic cardiomyopathy. Methods: This work included: one hundred and five rats which were divided equally into seven groups: healthy control group, diabetic group that was induced by streptozotocin, diabetic group received MSCs only, diabetic group received Pioglitazone(PPAR Þ agonist) only, diabetic group received both MSCs and Pioglitazone, diabetic group received Exendin-4 only, diabetic group received both MSCs and Exendin-4 . Histopathological examination, gene expression of light chain 3(LC3), beclin, PGC alpha, nuclear factor kappa-light- chain-enhancer of activated B cells (NFmB) and Myocyte enhancer factor- 2 (Mef2) genes by real time reverse transcription-polymerase chain reaction (RT-PCR) in rat heart tissue, uncoupler protein 2 (UCP2) by western blot technique, serum levels of Mitochondrial cardiolipin and insulin by ELISA were assessed
530 _aIssued also as CD
653 4 _aDiabetic cardiomyopathy
653 4 _aMSCs
653 4 _aPPAR у
700 0 _aMohamed Abdelaziz Wassef ,
_eSupervisor
700 0 _aOla Mostafa Tork ,
_eSupervisor
700 0 _aWalaa Ibrahim Ali ,
_eSupervisor
905 _aNazla
_eRevisor
905 _aShaima
_eCataloger
942 _2ddc
_cTH
999 _c60179
_d60179