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Simultaneous31P- and1H-Nuclear Magnetic Resonance Studies of Hypoxia and Ischemia in the Cat Brain
Author(s) -
László Gyulai,
Mitchell D. Schnall,
Alan C. McLaughlin,
John S. Leigh,
Britton Chance
Publication year - 1987
Publication title -
journal of cerebral blood flow and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.167
H-Index - 193
eISSN - 1559-7016
pISSN - 0271-678X
DOI - 10.1038/jcbfm.1987.103
Subject(s) - intracellular ph , cats , chemistry , ischemia , hypoxia (environmental) , acidosis , creatine kinase , lactate dehydrogenase , metabolism , nuclear magnetic resonance spectroscopy , creatine , medicine , endocrinology , intracellular , nuclear magnetic resonance , oxygen , biochemistry , biology , enzyme , physics , organic chemistry
The objective of this study was to evaluate simultaneous 31 P/ 1 H nuclear magnetic resonance (NMR) spectroscopy as a technique for monitoring and correlating changes in brain energy metabolism during hypoxia and ischemia. Five cats were studied with a protocol that involved 20 min of hypoxia (P a o 2 20 mm), 60 min of recovery, 10 min of hypoxia with relative ischemia (bilateral carotid occlusion, P a O 2 20 mm), and 60 min of recovery. Bifrontal and biparietal electrocorticograms (ECoG) were monitored continuously during the entire protocol. The results demonstrate that the degree of metabolic response is different in individual cats, but a number of quantitative relationships between metabolic parameters are consistently observed for all cats. First, there is agreement between increases in lactate and changes in intracellular pH; the observed relationship corresponds to an in vivo cerebral buffer capacity of 29 μmol/g/pH unit. Second, the delayed recovery of PCr is due to the effect of metabolic acidosis on the creatine kinase equilibrium and not to a delayed recovery of the ATP/ADP ratio. Third, the observed rate of lactate clearance from the cell is zero-order ( k = 0.36 μmol/g/min) for lactate levels >5 μm/g and may be composed of both lactate efflux from the cell and lactate oxidation.

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