Nuciferine Attenuates Doxorubicin-Induced Cardiotoxicity: An In Vitro and In Vivo Study.
Rajendran HarishkumarJohnsamuel Godwin ChristopherRajan RavindranChinnadurai Immanuel SelvarajPublished in: Cardiovascular toxicology (2021)
Chemotherapeutic drugs are a known factor that impairs the system of life due to their severe side effects. A more worrying fact is that the patients administered with doxorubicin fall under the risk of cardiotoxicity. The evolution of exploring plant-derived compounds is a possible way to combat health issues in therapeutic applications. Hence, this study focuses on the protective effect of plant-based compound nuciferine (NFN) against doxorubicin-induced cardiotoxicity in both in vitro and in vivo models. In this investigation, nuciferine significantly reduces DOX-mediated cardiotoxicity by mitigating reactive oxygen species, thereby preventing DNA fragmentation, regulating apoptosis genes and reducing the caspase 3/7 levels in vitro. Besides, nuciferine has shown significant protection against DOX-induced cardiac impairment and the upregulation of cardiogenic markers in vivo. The DOX-induced oxidative stress can be mitigated via enhancing the endogenous antioxidants, thereby controlling ROS-mediated apoptosis. In virtue of these potential features, nuciferine can be a budding candidate to address therapeutic needs.
Keyphrases
- high glucose
- reactive oxygen species
- diabetic rats
- cell death
- drug induced
- end stage renal disease
- healthcare
- drug delivery
- oxidative stress
- chronic kidney disease
- cancer therapy
- endothelial cells
- mental health
- cell proliferation
- peritoneal dialysis
- ejection fraction
- dna methylation
- risk assessment
- induced apoptosis
- poor prognosis
- atrial fibrillation
- early onset
- endoplasmic reticulum stress
- circulating tumor
- single molecule