Expression of Bax and Bcl-2 Proteins in Left-Ventricular Cardiomyocytes in Wistar-Kyoto and SHR Rats with Insulin-Dependent Diabetes Mellitus
Autor: | A. P. Sklifasovskaya, M. M. Azova, A. Yu. Ryabinina, M. L. Blagonravov, V. A. Goryachev |
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Rok vydání: | 2021 |
Předmět: |
medicine.medical_specialty
business.industry General Medicine Streptozotocin medicine.disease Essential hypertension General Biochemistry Genetics and Molecular Biology Pathogenesis Endocrinology Apoptosis Heart failure Internal medicine Insulin dependent diabetes Diabetes mellitus medicine Immunohistochemistry business medicine.drug |
Zdroj: | Bulletin of Experimental Biology and Medicine. 171:576-581 |
ISSN: | 1573-8221 0007-4888 |
Popis: | Loss of cardiomyocytes due to apoptotic or necrotic death is an important component of the pathogenesis of heart failure. Initiation of apoptosis by the mitochondrial pathway depends on the balance between proapoptotic and antiapoptotic factors, in particular, Bax and Bcl-2. Cardiomyocyte apoptosis in essential hypertension is studied in sufficient details. At the same time, apoptotic processes in the myocardium in diabetes mellitus alone and in combination with essential hypertension remain poorly understood. Here we studied the expression of Bax and Bcl-2 in the left ventricular cardiomyocytes of 38-week-old male Wistar-Kyoto rats and 38- and 57-week-old SHR rats with essential hypertension, diabetes mellitus, and a combination of these pathologies. Insulin-dependent diabetes mellitus was modelled by a single parenteral administration of streptozotocin in a dose 65 mg/kg. Expression of Bax and Bcl-2 was assessed by the immunohistochemical method. In essential hypertension and diabetes mellitus, the apoptotic processes in the ventricular myocardium were enhanced, as is seen from the increase in the content of the proapoptotic factor Bax and a decrease in the expression of the antiapoptotic factor Bcl-2. However, in case of combined pathology, Bax content increased less markedly, while the expression of antiapoptotic Bcl-2 was significantly increased. |
Databáze: | OpenAIRE |
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