Application | Comment | Organism |
---|---|---|
medicine | mice with targeted disruption of the Ephx2 gene coding for soluble epoxide hydrolase have normal heart anatomy and basal contractile function, but have higher fatty acid epoxide:diol ratios in plasma and cardiomyocytes cell culture media. The heart have improved recovery of left ventricular developed pressure and less infarction after 20 min ischemia, compared with wild-type. Perfusion with 14,15-epoxyeicosa-5(Z)-enoic acid before ischemia abolishes this cardioprotective phenotype. Enzyme null mice exhibit increased cardiac expression of glycogen synthase kinase-3beta phosphoprotein after ischemia | Mus musculus |
Protein Variants | Comment | Organism |
---|---|---|
additional information | mice with targeted disruption of the Ephx2 gene coding for soluble epoxide hydrolase have normal heart anatomy and basal contractile function, but have higher fatty acid epoxide:diol ratios in plasma and cardiomyocytes cell culture media. The heart have improved recovery of left ventricular developed pressure and less infarction after 20 min ischemia, compared with wild-type. Perfusion with 14,15-epoxyeicosa-5(Z)-enoic acid before ischemia abolishes this cardioprotective phenotype. Enzyme null mice exhibit increased cardiac expression of glycogen synthase kinase-3beta phosphoprotein after ischemia | Mus musculus |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Mus musculus | - |
- |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
heart | - |
Mus musculus | - |