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Mitochondrial K(ATP) channels and sarcoplasmic reticulum influence cardiac force development under anoxia in the Amazonian armored catfish Liposarcus pardalis.

Abstract
The contribution of alterations in mitochondrial K(ATP) channel activity and the sarcoplasmic reticulum (SR) to anaerobic cardiac function in the anoxia tolerant armored catfish Liposarcus pardalis were assessed. K(ATP) channels contribute to hypoxic cardioprotection in mammals, but little is known of their action in more hypoxia tolerant animals. Anoxia resulted in a decrease in force in isometrically contracting ventricle strips to approximately 40% of the pre-anoxic level. This was maintained for at least 2 h. Upon reoxygenation, hearts recovered to the same level as control preparations. Treatment with 5-hydroxydecanoic acid (5HD), a specific mitochondrial K(ATP) blocker significantly increased force in preparations during anoxia and caused hypercontracture at reoxygenation. Ryanodine, a specific inhibitor of SR function, significantly increased force loss in ventricle preparations under anoxia. Results show that mitochondrial K(ATP) channel activity and SR function are important in anaerobic and post-anaerobic contractility in armored catfish heart.
AuthorsTyson J MacCormack, Jason R Treberg, Vera M F Almeida-Val, Adalberto L Val, Willam R Driedzic
JournalComparative biochemistry and physiology. Part A, Molecular & integrative physiology (Comp Biochem Physiol A Mol Integr Physiol) Vol. 134 Issue 2 Pg. 441-8 (Feb 2003) ISSN: 1095-6433 [Print] United States
PMID12547274 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Decanoic Acids
  • Hydroxy Acids
  • Potassium Channel Blockers
  • Potassium Channels
  • Ryanodine
  • 5-hydroxydecanoic acid
  • Adenosine Triphosphate
  • Oxygen
Topics
  • Adenosine Triphosphate (metabolism)
  • Animals
  • Catfishes (metabolism, physiology)
  • Decanoic Acids (pharmacology)
  • Hydroxy Acids (pharmacology)
  • Hypoxia (metabolism, physiopathology)
  • In Vitro Techniques
  • Mitochondria, Heart (metabolism)
  • Myocardial Contraction (drug effects)
  • Oxygen (pharmacology)
  • Potassium Channel Blockers (pharmacology)
  • Potassium Channels (drug effects, metabolism)
  • Ryanodine (pharmacology)
  • Sarcoplasmic Reticulum (physiology)

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