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Adenylate cyclase 1 knockdown attenuates pirarubicin-induced cardiotoxicity.
- Source :
-
Clinical and experimental pharmacology & physiology [Clin Exp Pharmacol Physiol] 2024 Oct; Vol. 51 (10), pp. e13920. - Publication Year :
- 2024
-
Abstract
- This study aimed to investigate the effects and possible mechanisms of adenylate cyclase 1 (ADCY1) on pirarubicin-induced cardiomyocyte injury. HL-1 cells were treated with pirarubicin (THP) to induce intracellular toxicity, and the extent of damage to mouse cardiomyocytes was assessed using CCK-8, Edu, flow cytometry, ROS, ELISA, RT-qPCR and western blotting. THP treatment reduced the viability of HL-1 cells, inhibited proliferation, induced apoptosis and triggered oxidative stress. In addition, the RT-qPCR results revealed that ADCY1 expression was significantly elevated in HL-1 cells, and molecular docking showed a direct interaction between ADCY1 and THP. Western blotting showed that ADCY1, phospho-protein kinase A and GRIN2D expression were also significantly elevated. Knockdown of ADCY1 attenuated THP-induced cardiotoxicity, possibly by regulating the ADCY1/PKA/GRIN2D pathway.<br /> (© 2024 John Wiley & Sons Australia, Ltd.)
- Subjects :
- Animals
Mice
Cell Line
Apoptosis drug effects
Oxidative Stress drug effects
Oxidative Stress genetics
Molecular Docking Simulation
Cell Proliferation drug effects
Cell Survival drug effects
Cyclic AMP-Dependent Protein Kinases metabolism
Antineoplastic Agents pharmacology
Antineoplastic Agents toxicity
Adenylyl Cyclases metabolism
Adenylyl Cyclases genetics
Cardiotoxicity genetics
Doxorubicin toxicity
Doxorubicin pharmacology
Doxorubicin analogs & derivatives
Gene Knockdown Techniques
Myocytes, Cardiac drug effects
Myocytes, Cardiac metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1440-1681
- Volume :
- 51
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Clinical and experimental pharmacology & physiology
- Publication Type :
- Academic Journal
- Accession number :
- 39227014
- Full Text :
- https://doi.org/10.1111/1440-1681.13920