| Title | Myocardial ischemia activates the JAK-STAT pathway through angiotensin II signaling in in vivo myocardium of rats. | | Author(s) | Omura T, Yoshiyama M, Ishikura F, Kobayashi H, Takeuchi K, Beppu S, Yoshikawa J | | Institution | First Department of Internal Medicine, Osaka City University Medical School, Osaka, Japan. omura@med.osaka-cu.ac.jp | | Source | J Mol Cell Cardiol 2001 Feb; 33(2):307-16. | | MeSH | Angiotensin II
Animals
Antihypertensive Agents
Benzimidazoles
Blotting, Western
Coronary Vessels
DNA
DNA-Binding Proteins
Drosophila Proteins
Electrophoresis, Polyacrylamide Gel
Enzyme Activation
Enzyme Inhibitors
Guanine Nucleotide Exchange Factors
Imidazoles
Imidazolidines
Immunoblotting
Male
Myocardial Infarction
Myocardial Ischemia
Peptidyl-Dipeptidase A
Phosphorylation
Precipitin Tests
Protein-Tyrosine Kinase
Proto-Oncogene Proteins
Rats
Rats, Wistar
Receptor, Angiotensin, Type 1
Receptor, Angiotensin, Type 2
Receptors, Angiotensin
STAT1 Transcription Factor
STAT3 Transcription Factor
Signal Transduction
Tetrazoles
Time Factors
Trans-Activators
| | Abstract | There have been many studies concerning the hemodynamics and physiological mechanisms in ischemic heart disease, little is known about molecular mechanisms during myocardial ischemia in in vivo study. As the signal transduction pathway responsible for myocardial hypertrophy and apoptosis, janus kinase (JAK) and signal transducers and activators of transcription (STAT) are suggested to play an important role. However, whether in vivo activation of JAK-STAT pathway occurs during myocardial ischemia is still unknown. The purpose of this study was to determine whether myocardial JAK or STAT is activated in ischemic heart, and to evaluate the angiotensin blockade on the pathway. Myocardial infarction was produced by ligation of the coronary artery in Wistar rats. After myocardial ischemia, we analysed both activated levels and total amounts of JAK1, JAK2, STAT1 and STAT3 by Western blot analyses at 0, 5, 15, 30, 60, 120 and 240 min. Compared with JAK activities at 0 min, JAK1 activities were significantly increased at 60 and 120 min (3.0- and 3.7-fold, respectively, P<0.01). JAK2 and STAT1 activities of ischemic myocardium were unchanged through the time course. STAT3 activities were increased at 5 min (3.3-fold, P<0.01) and markedly enhanced at 30, 60 and 120 min (4.6-, 7.7- and 8.7-fold, respectively, P<0.01). Pretreatment with imidapril (ACE inhibitor) and candesartan cilexitil (AT1 receptor antagonist) significantly prevented the increase in the phosphorylation of JAK1 at 120 min and STAT3 at 30 and 120 min. Sis-inducing factor (SIF) DNA complex was supershifted by specific anti-STAT3 antibody, indicating that increased SIF complex at least contained activated STAT3 proteins in ischemic myocardium. Imidapril and candesartan cilexitil inhibited the activation of SIF DNA binding at 1 day after coronary ligation. In conclusion, we showed that JAK1 and STAT3 were activated by ischemia from the basal activities in in vivo rat myocardial ischemia model. Imidapril and candesartan cilexitil prevented the increase in phosphorylated JAK1 and STAT3, thereby suggesting that angiotensin II, especially angiotensin II type I receptor, partially mediates activation of myocardial JAK-STAT pathway in acute myocardial ischemia. | | Language | eng | | Pub Type(s) | Journal Article
| | PubMed ID | 11162135 |
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