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Perinatal Hypoxic‐Ischemic Brain Injury Enhances Quisqualic Acid‐Stimulated Phosphoinositide Turnover
Author(s) -
Chen ChuKuang,
Silverstein Faye S.,
Fisher Stephen K.,
Statman Daniel,
Johnston Michael V.
Publication year - 1988
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.1988.tb01046.x
Subject(s) - quisqualic acid , hypoxia (environmental) , glutamate receptor , endocrinology , medicine , ischemia , striatum , agonist , biology , anesthesia , chemistry , receptor , ampa receptor , dopamine , oxygen , organic chemistry
In an experimental model of perinatal hypoxic‐ischemic brain injury, we examined quisqualic acid (Quis)‐stimulated phosphoinositide (PPI) turnover in hippocampus and striatum. To produce a unilateral forebrain lesion in 7‐day‐old rat pups, the right carotid artery was ligated and animals were then exposed to moderate hypoxia (8% oxygen) for 2.5 h. Pups were killed 24 h later and Quis‐stimulated PPI turnover was assayed in tissue slices obtained from hippocampus and striatum, target regions for hypoxic‐ischemic injury. The glutamate agonist Quis (10 ‐4 M ) preferentially stimulated PPI hydrolysis in injured brain. In hippocampal slices of tissue derived from the right cerebral hemisphere, the addition of Quis stimulated accumulation of inositol phosphates by more than ninefold (1,053 ± 237% of basal, mean ± SEM, n = 9). In contrast, the addition of Quis stimulated accumulation of inositol phosphates by about fivefold in the contralateral hemisphere (588 ± 134%) and by about sixfold in controls (631 ± 177%, p < 0.005, comparison of ischemic tissue with control). In striatal tissue, the corresponding values were 801 ± 157%, 474 ± 89%, and 506 ± 115% (p < 0.05). In contrast, stimulation of PPI turnover elicited by the cho‐linergic agonist carbamoylcholine, (10 ‐4 or 10 ‐2 M ) was unaffected by hypoxia‐ischemia. The results suggest that prior exposure to hypoxia‐ischemia enhances coupling of excitatory amino acid receptors to phospholipase C activity. This activation may contribute to the pathogenesis of irreversible brain injury and/or to mechanisms of recovery.