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Anoxia and ischemia tolerance in turtle hearts
1Department of Veterinary Physiology and Pharmacology, Texas A&M University, College Station 77843-4466, USA.
Summary
Turtle hearts show remarkable anoxia tolerance through metabolic rate reduction and stable ATP levels. Key adaptations involve metabolic control, acid-base balance, and phospholipid homeostasis, though their interactions remain unclear.
Area of Science:
- Cardiovascular Physiology
- Comparative Physiology
- Biochemistry
Background:
- Turtle hearts possess exceptional tolerance to anoxia and ischemia.
- The underlying mechanisms for this resilience are not fully understood.
- A significant adaptation involves a rapid decrease in metabolic rate during anoxia.
Purpose of the Study:
- To investigate the physiological and biochemical mechanisms behind anoxia and ischemia tolerance in turtle hearts.
- To compare the anoxic responses of painted turtle (Chrysemys picta) and softshelled turtle (Trionyx spinifer) hearts.
- To explore the potential role of phosphodiesters (PDEs) in anoxia tolerance.
Main Methods:
- Nuclear magnetic resonance (NMR) measurements to assess high-energy phosphates (e.g., phosphocreatine [PCr], ATP) and intracellular pH (pHi).
- In vivo and isolated heart studies to evaluate cardiac performance and tolerance to anoxia/ischemia.
- Analysis of phosphodiester (PDE) concentrations.
Main Results:
- Painted turtle hearts exhibit a rapid decrease in PCr to 50% during anoxia, with ATP levels maintained and pHi decreasing slightly.
- Softshelled turtle hearts, while more sensitive in vivo, show similar anoxia tolerance in isolated preparations compared to painted turtle hearts.
- Little difference was observed in cardiac performance, high-energy phosphates, or pHi between species during ischemia.
Conclusions:
- Turtle hearts maintain metabolic control, acid-base, and phospholipid homeostasis during anoxia/ischemia.
- These interdependent physiological processes contribute to anoxia and ischemia tolerance.
- Further research is needed to elucidate the complex interactions of these mechanisms and the specific role of PDEs.