A new approach of nano-metformin as a protector against radiation-induced cardiac fibrosis and inflammation via CXCL1/TGF-Β pathway.
Heba M KaramDina M LotfyAyman A IbrahimFarag M MosallamSahar S AbdelrahmanAmira Abd-ElRaoufPublished in: Naunyn-Schmiedeberg's archives of pharmacology (2024)
The present work investigates the potential role of metformin nanoparticles (MTF-NPs) as a radio-protector against cardiac fibrosis and inflammation induced by gamma radiation via CXCL1/TGF-β pathway. Lethal dose fifty of nano-metformin was determined in mice, then 21 rats (male albino) were equally divided into three groups: normal control (G1), irradiated control (G2), and MTF-NPs + IRR (G3). The possible protective effect of MTF-NPs is illustrated via decreasing cardiac contents of troponin, C-X-C motif Ligand 1 (CXCL1), tumor growth factor β (TGF-β), protein kinase B (AKT), and nuclear factor-κB (NF-κB). Also, the positive effect of MTF-NPs on insulin-like growth factor (IGF) and platelet-derived growth factor (PDGF) in heart tissues using immunohistochemical technique is illustrated in the present study. Histopathological examination emphasizes the biochemical findings. The current investigation suggests that MTF-NPs might be considered as a potent novel treatment for the management of cardiac fibrosis and inflammation in patients who receive radiotherapy or workers who may be exposed to gamma radiation.
Keyphrases
- growth factor
- radiation induced
- nuclear factor
- oxidative stress
- left ventricular
- signaling pathway
- transforming growth factor
- radiation therapy
- oxide nanoparticles
- toll like receptor
- heart failure
- protein kinase
- gene expression
- cell proliferation
- type diabetes
- epithelial mesenchymal transition
- pi k akt
- immune response
- locally advanced
- anti inflammatory
- smoking cessation
- binding protein
- combination therapy
- growth hormone
- walled carbon nanotubes