Indoline derivatives mitigate liver damage in a mouse model of acute liver injury

Keyphrases

• Interleukin-6 100%
• Mouse Model 100%
• Liver 100%
• Liver Damage 100%
• Indoline Derivatives 100%
• D-galactosamine 100%
• Acute Liver Injury 100%
• Apoptosis 66%
• Lipopolysaccharide 66%
• Alanine Aminotransferase 66%
• Acute Liver Failure 66%
• Aspartate Aminotransferase 66%
• Phosphorylation 33%
• Liver Enzymes 33%
• Macrophages 33%
• Reduced Mortality 33%
• Tissue Damage 33%
• DNA Binding 33%
• Hematoxylin 33%
• Eosin 33%
• Caspase-3 33%
• Cleaved caspase-3 33%
• Intraperitoneal Injection 33%
• Lipopolysaccharide-induced 33%
• Anti-inflammatory Activity 33%
• Anti-inflammatory Agents 33%
• Balb C Mice 33%
• Transcription Factor AP-1 33%
• Background Exposure 33%
• MAPK p38 33%

Pharmacology, Toxicology and Pharmaceutical Science

• Mouse Model 100%
• Liver Injury 100%
• Tumor Necrosis Factor 100%
• Mouse 60%
• Galactosamine 60%
• Lipopolysaccharide 60%
• Aspartate Aminotransferase 40%
• Alanine Aminotransferase 40%
• Acute Liver Failure 40%
• Caspase 3 40%
• Anti-Inflammatory Drug 20%
• Antiinflammatory Agent 20%
• Liver Enzyme 20%
• Intraperitoneal Injection 20%
• Tissue Injury 20%
• Transcription Factor AP 1 20%
• Dexamethasone 20%
• Haematoxylin 20%
• Eosin 20%