Brief Article
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World J Crit Care Med. Nov 4, 2013; 2(4): 56-64
Published online Nov 4, 2013. doi: 10.5492/wjccm.v2.i4.56
Pyruvate-fortified resuscitation stabilizes cardiac electrical activity and energy metabolism during hypovolemia
Hunaid A Gurji, Daniel W White, Besim Hoxha, Jie Sun, Albert H Olivencia-Yurvati, Robert T Mallet
Hunaid A Gurji, Daniel W White, Jie Sun, Albert H Olivencia-Yurvati, Robert T Mallet, Departments of Integrative Physiology, University of North Texas Health Science Center, Fort Worth, TX 76107, United States
Besim Hoxha, Robert T Mallet, Olivencia-Yurvati, Departments of Surgery, University of North Texas Health Science Center, Fort Worth, TX 76107, United States
Albert H Olivencia-Yurvati, Robert T Mallet, Cardiovascular Research Institute, University of North Texas Health Science Center, Fort Worth, TX 76107, United States
Robert T Mallet, Institute for Aging and Alzheimer’s Research, University of North Texas Health Science Center, Fort Worth, TX 76107, United States
Author contributions: Gurji HA, White DW, Hoxha B, Olivencia-Yurvati AH, Mallet RT designed the research; Gurji HA, White DW, Hoxha B conducted the surgical preparation and experimental protocols; Gurji HA, Sun J performed analytical measurements; Gurji HA, Sun J analyzed the data and prepared the figures; Gurji HA, Olivencia-Yurvati AH, Mallet RT wrote the manuscript.
Supported by Grant #W911NF0910086 from the United States Department of Defense; Predoctoral fellowships from the Graduate School of Biomedical Sciences, University of North Texas Health Science Center to Gurji HA and White DW
Correspondence to: Robert T Mallet, PhD, Department of Integrative Physiology, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107-2699, United States. robert.mallet@unthsc.edu
Telephone: +1-817-7352260 Fax: +1-817-7355084
Received: May 7, 2013
Revised: July 20, 2013
Accepted: August 12, 2013
Published online: November 4, 2013
Processing time: 177 Days and 11.2 Hours
Abstract

AIM: To test the hypothesis that fluid resuscitation with Ringer’s solution enriched with pyruvate (PR), a physiological antioxidant and energy substrate, affords protection of myocardial metabolism and electrophysiological performance superior to lactated Ringer’s (LR) during hypovolemia and hindlimb ischemia-reperfusion.

METHODS: Male domestic goats (25-30 kg) were exsanguinated to a mean arterial pressure of 48 ± 1 mmHg. Right hindlimb ischemia was imposed for 90 min by applying a tourniquet and femoral crossclamp. LR or PR, infused iv, delivered 0.05 mmol/kg per minute L-lactate or pyruvate, respectively, from 30 min hindlimb ischemia until 30 min post-ischemia. Time controls (TC) underwent neither hemorrhage, hindlimb ischemia nor resuscitation. Goats were sacrificed and left ventricular myocardium biopsied at 90 min fluid resuscitation (n = 6 per group) or 3.5 h later (n = 9 LR, 10 PR, 8 TC).

RESULTS: Myocardial 8-isoprostane content, phosphocreatine phosphorylation potential, creatine kinase activity, and heart rate-adjusted QT interval (QTc) variability were evaluated at 90 min resuscitation and 3.5 h post-resuscitation. PR sharply lowered pro-arrhythmic QTc variability vs LR (P < 0.05); this effect persisted 3.5 h post-resuscitation. PR lowered myocardial 8-isoprostane content, a product of oxidative stress, by 39 and 37% during and 3.5 h after resuscitation, respectively, vs LR. Creatine kinase activity fell 42% post-LR vs TC (P < 0.05), but was stable post-PR (P < 0.02 vs post-LR). PR doubled phosphocreatine phosphorylation potential, a measure of ATP free energy state, vs TC and LR (P < 0.05); this energetic enhancement persisted 3.5 h post-resuscitation.

CONCLUSION: By augmenting myocardial energy state and protecting creatine kinase activity, pyruvate-enriched resuscitation stabilized cardiac electrical function during central hypovolemia and hindlimb ischemia-reperfusion.

Keywords: Creatine kinase; Electrocardiogram; Hypovolemia; 8-Isoprostane; Phosphocreatine; Reactive oxygen species; Ringer’s lactate

Core tip: In goats subjected to exsanguination-induced hypovolemia and tourniquet-imposed hindlimb ischemia-reperfusion, intravenous resuscitation with Ringer’s lactate produced marked electrocardiographic instability, lipid peroxidation and inactivation of the critical creatine kinase system, which supplies energy for membrane ion transport. In comparison with lactated Ringer’s, resuscitation enriched with the natural antioxidant and energy substrate pyruvate stabilized cardiac rhythm, prevented lipid peroxidation, preserved creatine kinase activity and augmented myocardial energy reserves. Importantly, these favorable effects persisted for at least 3.5 h after terminating pyruvate-enriched resuscitation. Thus, pyruvate-enriched resuscitation prevented creatine kinase inactivation by oxidative stress, thereby preventing cardiac rhythm disturbances after central hypovolemia.