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Chitosan Versus Dapagliflozin in a Diabetic Cardiomyopathy Mouse Model.
Târtea, Georgica; Popa-Wagner, Aurel; Sfredel, Veronica; Mitran, Smaranda Ioana; Dan, Alexandra Oltea; Țuca, Anca-Maria; Preda, Alexandra Nicoleta; Raicea, Victor; Țieranu, Eugen; Cozma, Dragoș; Vatașescu, Radu.
Afiliación
  • Târtea G; Department of Physiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
  • Popa-Wagner A; Department of Neurology, University Hospital Essen, University of Duisburg-Essen, 45147 Essen, Germany.
  • Sfredel V; Department of Physiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
  • Mitran SI; Department of Physiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
  • Dan AO; Department of Physiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
  • Țuca AM; Department of Physiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
  • Preda AN; Department of Physiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
  • Raicea V; Department of Cardiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
  • Țieranu E; Department of Cardiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
  • Cozma D; Department of Cardiology, "Victor Babes" University of Medicine and Pharmacy, 2 Eftimie Murgu Sq., 300041 Timisoara, Romania.
  • Vatașescu R; Cardio-Thoracic Pathology Department, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Int J Mol Sci ; 25(4)2024 Feb 09.
Article en En | MEDLINE | ID: mdl-38396795
ABSTRACT
Diabetes mellitus is a metabolic disorder with global economic implications that can lead to complications such as diabetic cardiomyopathy. The aim of this study was to compare the effects of chitosan versus dapagliflozin in mouse diabetic cardiomyopathy. We used 32 C57Bl/6 male mice aged between 8 and 10 weeks, which were randomly divided into Control-without diabetes mellitus (DM), type 1 DM (T1DM), T1DM + Chitosan, and T1DM + Dapapgliflozin groups. We induced diabetes with streptozotocin and treated the animals for 12 weeks. The analysis showed a reduction in intramyocardial fibrosis in the T1DM + Dapapgliflozin compared to T1DM animals. In T1DM + CHIT, a reduction in intramyocardial fibrosis was observed although, accordingly, there was also no significant decrease in blood glucose. The level of oxidative stress was reduced in the groups of treated animals compared to T1DM. All these observed changes in the structure and function of hearts were highlighted in the echocardiographic examination. In the treated groups, there was delayed appearance of left ventricular (LV) hypertrophy, a slight decrease in the ejection fraction of the LV, and an improved diastolic profile. The results demonstrate that chitosan has promising effects on diabetic cardiomyopathy that are comparable to the beneficial effects of dapagliflozin.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Compuestos de Bencidrilo / Quitosano / Diabetes Mellitus Tipo 1 / Cardiomiopatías Diabéticas / Glucósidos Límite: Animals Idioma: En Revista: Int J Mol Sci Año: 2024 Tipo del documento: Article País de afiliación: Rumanía

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Compuestos de Bencidrilo / Quitosano / Diabetes Mellitus Tipo 1 / Cardiomiopatías Diabéticas / Glucósidos Límite: Animals Idioma: En Revista: Int J Mol Sci Año: 2024 Tipo del documento: Article País de afiliación: Rumanía