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Protective effects of 3,6-dimethylamino-dibenzopyriodonium edetate on global ischemia reperfused isolated rat hearts.

Abstract
The effects of 3,6-dimethylamino-dibenzopyriodonium edetate (IHC-72) on global ischemia reperfused rat hearts were investigated. In the isolated working rat heart, 40-min global ischemia followed by 30-min reperfusion resulted in increases of ventricular tachycardia (VT) and ventricular fibrillation (VF), increases of creatine kinase (CK) release and malondialdehyde (MDA) contents, but decreased superoxide dismutase (SOD) activity. Following ischemia and reperfusion, the accumulation of myocardial calcium increased. IHC-72 50 mumol.L-1 given 10 min before ischemia and during reperfusion decreased the cardiac CK release, VT, and VF, reduced the MDA contents, prevented the reduction of SOD activity and attenuated the accumulation of myocardial calcium and sodium vs control. These results indicated that IHC-72 protected myocardial reperfused injury.
AuthorsG J Ji, J Z Zhang, D Q Liu, D H Zhao, B H Sheng
JournalZhongguo yao li xue bao = Acta pharmacologica Sinica (Zhongguo Yao Li Xue Bao) Vol. 14 Issue 3 Pg. 206-10 (May 1993) ISSN: 0253-9756 [Print] China
PMID8237392 (Publication Type: Journal Article)
Chemical References
  • Anti-Arrhythmia Agents
  • Onium Compounds
  • 3,6-dimethylaminodibenzopyridonium edetate
  • Malondialdehyde
  • Edetic Acid
  • Verapamil
  • Superoxide Dismutase
  • Creatine Kinase
  • Calcium
Topics
  • Animals
  • Anti-Arrhythmia Agents (pharmacology, therapeutic use)
  • Calcium (metabolism)
  • Coronary Circulation (drug effects)
  • Creatine Kinase (metabolism)
  • Edetic Acid (analogs & derivatives, pharmacology, therapeutic use)
  • In Vitro Techniques
  • Male
  • Malondialdehyde (metabolism)
  • Myocardial Reperfusion Injury (metabolism, prevention & control)
  • Myocardium (metabolism)
  • Onium Compounds (pharmacology, therapeutic use)
  • Rats
  • Rats, Sprague-Dawley
  • Superoxide Dismutase (metabolism)
  • Verapamil (pharmacology)

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