Abstract |
Anesthetized open-chest dogs were subjected to 15-min myocardial ischemia followed by 2-h reperfusion to induce myocardial stunning. A novel Na(+)/H(+) exchange inhibitor 6,7,8,9-tetrahydro-2-methyl-5H-cyclohepta[ b]pyridine-3-carbonylguanidine maleate (TY-12533), administered 10 min before or 10 min after start of ischemia (3 mg/kg/10 min, i.v.), did not affect reductions in regional myocardial wall thickening, blood flow and pH during ischemia, but it significantly improved recovery of the wall thickening and blood flow after reperfusion. These results indicate that TY-12533, even when administered during ischemia, could prevent myocardial stunning without affecting myocardial dysfunction or acidosis induced by brief ischemia.
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Authors | K Aihara, H Hisa, J Sasamori, F Yoneyama, F Yamaguchi, I Satoh, S Satoh |
Journal | European journal of pharmacology
(Eur J Pharmacol)
Vol. 419
Issue 1
Pg. 93-7
(May 04 2001)
ISSN: 0014-2999 [Print] Netherlands |
PMID | 11348635
(Publication Type: Journal Article)
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Chemical References |
- Anti-Arrhythmia Agents
- Guanidines
- Pyridines
- Sodium-Hydrogen Exchangers
- TY 12533
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Topics |
- Animals
- Anti-Arrhythmia Agents
(pharmacology)
- Coronary Circulation
(drug effects)
- Dogs
- Female
- Guanidines
(pharmacology)
- Heart
(drug effects)
- Hydrogen-Ion Concentration
- Male
- Myocardial Stunning
(physiopathology, prevention & control)
- Myocardium
(metabolism)
- Pyridines
(pharmacology)
- Sodium-Hydrogen Exchangers
(antagonists & inhibitors)
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