The specific aim of this study is to understand the energetic and regulatory mechanisms that permit hearts of hypoxia tolerant vertebrates to function under conditions of hypoxia and acidosis that are rapidly fatal to hearts from hypoxia sensitive animals. Two sets of direct comparisons are planned at appropriate physiologic temperatures: (l) the hypoxia tolerant painted turtle (Chrysemys picta belli) compared to the more hypoxia sensitive softshelled turtle (Trionyx spinifer) at 20 degrees C; and (2) the hypoxia tolerant neonatal rabbit compared to the highly hypoxia sensitive adult rabbit at 38 degrees C. Classic in vitro physiologic and biochemical methods along with nuclear magnetic resonance spectroscopy will be used to examine pH and ionic regulation, cardiac energy state, and myocardial metabolic rate in isolated hearts from these animal models during hypoxia and acidosis and during recovery. These experiments will test the hypotheses that key adaptations to hypoxia and acidosis include reduced cellular energy metabolism, effective cell pH regulation, and effective cell calcium and sodium homeostasis. Studies of extreme hypoxia are severely limited in adult mammalian preparations because of their rapidly failing function. Painted turtles, because of their remarkable adaptations are an exceptional model system for studying these fundamental problems. Neonatal mammals, while less hypoxia tolerant than turtles, are still far better able to deal with the stresses of extreme hypoxia and acidosis than are adults. Many human pathologic conditions result in hypoxic and acidotic insults to the heart and it would be of-great clinical value to develop methods of protecting this sensitive tissue from the deleterious effects of these stresses. The potential significance of this research is that lessons learned from hypoxia tolerant hearts can provide a more fundamental understanding of the limitations of the human heart to hypoxia and acidosis and can suggest rational strategies for counteracting them in clinical, surgical, or organ bank settings.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
7R29HL045257-02
Application #
3473275
Study Section
Cardiovascular and Renal Study Section (CVB)
Project Start
1993-02-01
Project End
1998-01-31
Budget Start
1993-02-01
Budget End
1994-01-31
Support Year
2
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Texas A&M University
Department
Type
Schools of Veterinary Medicine
DUNS #
City
College Station
State
TX
Country
United States
Zip Code
77845
Chang, J; Wasser, J S; Cornelussen, R N et al. (2001) Activation of heat-shock factor by stretch-activated channels in rat hearts. Circulation 104:209-14
Wasser, J S; Vogel, L; Guthrie, S S et al. (1997) 31P-NMR determinations of cytosolic phosphodiesters in turtle hearts. Comp Biochem Physiol A Physiol 118:1193-200
Wasser, J S; Guthrie, S S; Chari, M (1997) In vitro tolerance to anoxia and ischemia in isolated hearts from hypoxia sensitive and hypoxia tolerant turtles. Comp Biochem Physiol A Physiol 118:1359-70
Wasser, J S (1996) Maintenance of cardiac function during anoxia in turtles: from cell to organism. Comp Biochem Physiol B Biochem Mol Biol 113:15-22
Wasser, J S (1995) Anoxia and ischemia tolerance in turtle hearts. Braz J Med Biol Res 28:1233-40