Metabolic responses in ischemic myocardium after inhalation of carbon monoxide.

Abstract

BACKGROUND:

To clarify the mechanisms of carbon monoxide (CO) tissue-protective effects, we studied energy metabolism in an animal model of acute coronary occlusion and pre-treatment with CO.

METHODS:

In anesthetized pigs, a coronary snare and microdialysis probes were placed. CO (carboxyhemoglobin 5%) was inhaled for 200 min in test animals, followed by 40 min of coronary occlusion. Microdialysate was analyzed for lactate and glucose, and myocardial tissue samples were analyzed for adenosine tri-phosphate, adenosine di-phosphate, and adenosine mono-phosphate.

RESULTS:

Lactate during coronary occlusion was approximately half as high in CO pre-treated animals and glucose levels decreased to a much lesser degree during ischemia. Energy charge was no different between groups.

CONCLUSIONS:

CO in the low-doses tested in this model results in a more favorable energy metabolic condition in that glycolysis is decreased in spite of maintained energy charge. Further work is warranted to clarify the possible mechanistic role of energy metabolism for CO protection.

• Authors: K Ahlström, B Biber, A Aberg, A Waldenström, G Ronquist, P Abrahamsson, P Strandén, G Johansson, M F Haney
• Journal: Acta anaesthesiologica Scandinavica (Acta Anaesthesiol Scand) Vol. 53 Issue 8 Pg. 1036-42 (Sep 2009) ISSN: 1399-6576 [Electronic] England
• PMID: 19426237 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Protective Agents
• Lactic Acid
• Adenosine Diphosphate
• Carbon Monoxide
• Pyruvic Acid
• Adenosine Triphosphate
• Carboxyhemoglobin
• Glucose

Topics

• Adenosine Diphosphate (metabolism)
• Adenosine Triphosphate (metabolism)
• Animals
• Blood Pressure (drug effects, physiology)
• Carbon Monoxide (pharmacology)
• Carboxyhemoglobin (metabolism)
• Central Venous Pressure (drug effects)
• Energy Metabolism (drug effects)
• Female
• Glucose (metabolism)
• Heart Rate (drug effects, physiology)
• Lactic Acid (metabolism)
• Microdialysis
• Myocardial Ischemia (metabolism)
• Myocardium (metabolism)
• Protective Agents
• Pyruvic Acid (metabolism)
• Swine