Assessing the protective effects of nanoceria on angiotensin II-induced cardiac injury in H9c2 cardiomyoblasts using proteomic analysis
- Rukhsana Gul 1, Hicham Benabdelkamel 1, Mushtaq A Dar 2, Afshan Masood 1, Meshail Okla 3, Ibrahim O Alanazi 4, Assim A Alfadda 5
- 1Proteomics unit, Obesity Research Center, College of Medicine, King Saud University, PO Box 2925, Riyadh 11461, Saudi Arabia.
- 2Center of Excellence for Research in Engineering Materials (CEREM), Deanship of Scientific Research (DSR), King Saudi University, Riyadh 11421, Saudi Arabia.
- 3Department of Community Health Sciences, College of Applied Medical Sciences, King Saud University, P.O. Box 22452, Riyadh 11495, Saudi Arabia.
- 4Healthy Aging Research Institute, Health Sector, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
- 5Proteomics unit, Obesity Research Center, College of Medicine, King Saud University, PO Box 2925, Riyadh 11461, Saudi Arabia; Department of Medicine, College of Medicine, King Saud University, PO Box 2925, Riyadh 11461, Saudi Arabia.
- 0Proteomics unit, Obesity Research Center, College of Medicine, King Saud University, PO Box 2925, Riyadh 11461, Saudi Arabia.
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View abstract on PubMed
Summary
This summary is machine-generated.Cerium oxide nanoparticles (nanoceria) show protective effects against angiotensin II (Ang II) induced cardiovascular damage. Nanoceria pretreatment reversed Ang II-induced protein changes linked to oxidative stress in H9c2 cardiomyoblasts.
Area Of Science
- Biochemistry
- Nanomedicine
- Cardiovascular Research
Background
- Angiotensin II (Ang II) stimulation causes oxidative stress and inflammation, contributing to cardiovascular diseases.
- Cerium oxide nanoparticles (nanoceria) possess antioxidant properties and show potential for mitigating Ang II's harmful effects.
Purpose Of The Study
- To investigate the protective effects of nanoceria against Ang II-induced pathology in H9c2 cardiomyoblasts.
- To compare proteomic changes induced by Ang II alone versus nanoceria pretreatment followed by Ang II stimulation.
Main Methods
- Proteomic analysis using 2D-DIGE to visualize differentially expressed proteins.
- Protein identification via MALDI-TOF mass spectrometry.
- Statistical analysis including PCA, hierarchical clustering, and canonical pathway analysis.
Main Results
- 118 differentially expressed protein spots were identified between control, Ang II-treated, and nanoceria-pretreated groups.
- Ang II upregulated proteins associated with oxidative stress, while nanoceria pretreatment downregulated these and upregulated defense proteins.
- 18 proteins were downregulated and 35 upregulated in the nanoceria pretreated Ang II group compared to Ang II alone.
Conclusions
- This study reveals complex proteomic alterations in H9c2 cardiomyoblasts due to Ang II.
- Nanoceria demonstrate significant protective effects by counteracting Ang II-induced oxidative stress and promoting defense mechanisms.
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