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Expression of Flk-1 and Cyclin D2 mRNA in the Myocardium of Rats with Doxorubicin-Induced Cardiomyopathy and after Treatment with Betulonic Acid Amide.
- Source :
-
Bulletin of experimental biology and medicine [Bull Exp Biol Med] 2017 Oct; Vol. 163 (6), pp. 809-813. Date of Electronic Publication: 2017 Oct 24. - Publication Year :
- 2017
-
Abstract
- The expression of VEGFR2 (Flk-1, according to immunohistochemistry) and of cyclin D2 mRNA (according to real-time PCR) in the myocardium of rats is studied in doxorubicin-induced cardiomyopathy and in response to betulonic acid amide. Doxorubicin alone and in combination with betulonic acid amide causes after 3 days a manifest reduction of cyclin D2 mRNA expression (by 38 and 63%, respectively), while injection of betulonic acid amide alone causes a 23-fold increase of cyclin D2 mRNA expression. An increase of cyclin D2 mRNA expression has been detected in all experimental groups after 14 days of experiment, the most pronounced in response to betulonic acid amide (63 times). The expression of Flk-1 in cardiomyocytes increases significantly in response to both chemical agents starting from day 3 of experiment. These results indicate that doxorubicin and betulonic acid amide induce cytoprotective reactions in the myocardium, first at the intracellular, then at the cellular levels.
- Subjects :
- Amides chemical synthesis
Animals
Cardiomyopathies chemically induced
Cardiomyopathies genetics
Cardiomyopathies pathology
Cardiotonic Agents chemical synthesis
Cyclin D2 agonists
Cyclin D2 antagonists & inhibitors
Cyclin D2 metabolism
Doxorubicin antagonists & inhibitors
Doxorubicin toxicity
Gene Expression Regulation
Male
Myocardium metabolism
Myocardium pathology
Myocytes, Cardiac drug effects
Myocytes, Cardiac metabolism
Myocytes, Cardiac pathology
Oleanolic Acid chemical synthesis
Oleanolic Acid pharmacology
RNA, Messenger agonists
RNA, Messenger antagonists & inhibitors
RNA, Messenger genetics
RNA, Messenger metabolism
Rats
Rats, Wistar
Signal Transduction
fms-Like Tyrosine Kinase 3 agonists
fms-Like Tyrosine Kinase 3 antagonists & inhibitors
fms-Like Tyrosine Kinase 3 metabolism
Amides pharmacology
Cardiomyopathies drug therapy
Cardiotonic Agents pharmacology
Cyclin D2 genetics
Oleanolic Acid analogs & derivatives
fms-Like Tyrosine Kinase 3 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1573-8221
- Volume :
- 163
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Bulletin of experimental biology and medicine
- Publication Type :
- Academic Journal
- Accession number :
- 29063324
- Full Text :
- https://doi.org/10.1007/s10517-017-3909-5