In vivo and in situ NMR studies are carried out on systems ranging from cell suspensions to perfused organs, to intact, anesthetized experimental animals in order to determine the mechanisms by which environmental chemicals and other types of stress irreversibly injure cells. Physiological, biochemical, and magnetic resonance measurements are carried out in parallel when possible, both to validate the techniques used, and more importantly, to correlate various metabolic changes in order to determine which factors may play a causative role. It has recently been suggested that perturbations in the level of cytosolic calcium ions may be of central importance in the production of irreversible cell injury arising from a variety of agents as a consequence of the activation of various catabolic, calcium dependent enzymes such as calpain and phospholipases. The level of cytosolic calcium ions in various preparations, particularly perfused rat hearts, has been determined based on the use of fluorine-19 NMR measurements of hearts loaded with fluorinated calcium chelator. Using this approach, the diastolic calcium level was determined to be 150 mM. Cytosolic calcium rose to approximately 2.5 uM after 15 minutes of ischemia, a time period shorter than required to irreversibly injure the heart, as determined by the leakage of cellular enzymes. Manipulations such as the introduction of calcium channel blockers, cardioplegic arrest, and low temperature, which delay the onset of irreversible injury, all correspondingly delay the rise of cytosolic calcium.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Intramural Research (Z01)
Project #
1Z01ES010004-10
Application #
3918601
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
10
Fiscal Year
1988
Total Cost
Indirect Cost
Name
U.S. National Inst of Environ Hlth Scis
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Shiva, Sruti; Huang, Zhi; Grubina, Rozalina et al. (2007) Deoxymyoglobin is a nitrite reductase that generates nitric oxide and regulates mitochondrial respiration. Circ Res 100:654-61
Huss, Janice M; Imahashi, Ken-ichi; Dufour, Catherine R et al. (2007) The nuclear receptor ERRalpha is required for the bioenergetic and functional adaptation to cardiac pressure overload. Cell Metab 6:25-37
Delozier, Tracy C; Kissling, Grace E; Coulter, Sherry J et al. (2007) Detection of human CYP2C8, CYP2C9, and CYP2J2 in cardiovascular tissues. Drug Metab Dispos 35:682-8
Murphy, Elizabeth; Steenbergen, Charles (2007) Cardioprotection in females: a role for nitric oxide and altered gene expression. Heart Fail Rev 12:293-300
Murphy, Elizabeth; Steenbergen, Charles (2007) Gender-based differences in mechanisms of protection in myocardial ischemia-reperfusion injury. Cardiovasc Res 75:478-86
Murphy, Elizabeth; Steenbergen, Charles (2007) Preconditioning: the mitochondrial connection. Annu Rev Physiol 69:51-67
Nikolic, Ivana; Liu, Dianxin; Bell, Jamie A et al. (2007) Treatment with an estrogen receptor-beta-selective agonist is cardioprotective. J Mol Cell Cardiol 42:769-80
Seubert, John M; Sinal, Christopher J; Graves, Joan et al. (2006) Role of soluble epoxide hydrolase in postischemic recovery of heart contractile function. Circ Res 99:442-50
Sun, Junhui; Picht, Eckard; Ginsburg, Kenneth S et al. (2006) Hypercontractile female hearts exhibit increased S-nitrosylation of the L-type Ca2+ channel alpha1 subunit and reduced ischemia/reperfusion injury. Circ Res 98:403-11
Sun, Junhui; Steenbergen, Charles; Murphy, Elizabeth (2006) S-nitrosylation: NO-related redox signaling to protect against oxidative stress. Antioxid Redox Signal 8:1693-705

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