acrolein has been researched along with Injury, Myocardial Reperfusion in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Chu, L; Han, X; Li, L; Liu, Y; Qi, J; Qu, W; Yang, Y; Zheng, B | 1 |
Bae, KH; Chang, KC; Hwa, JS; Jin, YC; Kim, HJ; Kim, YM; Kim, YS; Ko, YS; Lee, JH; Lee, YS; Ngoc, TM; Shi, LY | 1 |
Bhatnagar, A; Bolli, R; Guo, Y; Prabhu, SD; Tsai, LL; Vondriska, TM; Wang, GW; Zhang, J; Zhang, S; Zong, NC | 1 |
3 other study(ies) available for acrolein and Injury, Myocardial Reperfusion
Article | Year |
---|---|
Mechanisms of cinnamic aldehyde against myocardial ischemia/hypoxia injury in vivo and in vitro: Involvement of regulating PI3K/AKT signaling pathway.
Topics: Acrolein; Animals; Animals, Outbred Strains; Apoptosis; Cell Line; Creatine Kinase; Dose-Response Relationship, Drug; L-Lactate Dehydrogenase; Male; Mice; Myocardial Ischemia; Myocardial Reperfusion Injury; Oxidative Stress; Phosphatidylinositol 3-Kinases; Proto-Oncogene Proteins c-akt; Random Allocation | 2022 |
2-methoxycinnamaldehyde from Cinnamomum cassia reduces rat myocardial ischemia and reperfusion injury in vivo due to HO-1 induction.
Topics: Acrolein; Animals; Anti-Inflammatory Agents; Antioxidants; Cardiotonic Agents; Cinnamomum aromaticum; Coculture Techniques; Disease Models, Animal; Dose-Response Relationship, Drug; Enzyme Induction; Enzyme Inhibitors; Heme Oxygenase (Decyclizing); Heme Oxygenase-1; Hemodynamics; HMGB1 Protein; Human Umbilical Vein Endothelial Cells; Humans; Male; Myocardial Infarction; Myocardial Reperfusion Injury; Myocardium; Neutrophil Infiltration; NF-kappa B; Oxidative Stress; Plant Extracts; Plants, Medicinal; Rats; Rats, Sprague-Dawley; RNA Interference; Superoxide Dismutase; Time Factors; Transfection; Troponin I; Tumor Necrosis Factor-alpha; U937 Cells; Vascular Cell Adhesion Molecule-1; Ventricular Function, Left; Ventricular Pressure | 2012 |
Acrolein consumption exacerbates myocardial ischemic injury and blocks nitric oxide-induced PKCepsilon signaling and cardioprotection.
Topics: Acrolein; Animals; Cardiotonic Agents; Diet; Dose-Response Relationship, Drug; Mice; Mice, Inbred ICR; Mitochondria, Heart; Myocardial Infarction; Myocardial Reperfusion Injury; Myocardium; Protein Kinase C-epsilon; Protein Transport; Signal Transduction; Triazenes | 2008 |