Axon Conduction and Survival in CNS White Matter During Energy Deprivation: A Developmental Study
- 1 January 1998
- journal article
- research article
- Published by American Physiological Society in Journal of Neurophysiology
- Vol. 79 (1) , 95-105
- https://doi.org/10.1152/jn.1998.79.1.95
Abstract
Fern, Robert, Peter Davis, Stephen G. Waxman, and Bruce R. Ransom. Axon conduction and survival in CNS white matter during energy deprivation: a developmental study. J. Neurophysiol. 79: 95–105, 1998. We investigated the postnatal development of axon sensitivity to the withdrawal of oxygen, glucose, or the combined withdrawal of oxygen + glucose in the isolated rat optic nerve (a CNS white matter tract). Removal of either oxygen or glucose for 60 min resulted in irreversible injury in optic nerves from adult rats, assessed by loss of the evoked compound action potential (CAP). Optic nerves at ages 45 min caused the selective loss of late CAP components; this was not seen with oxygen deprivation. The amplitude of the early component recovered to 94.8% of control after 60 min of glucose withdrawal, although total CAP area recovered to only 42.3%. Combined oxygen + glucose withdrawal for 60 min produced a greater degree of permanent CAP loss than 60 min of glucose or oxygen withdrawal individually in optic nerves from rats older than P4. Younger than P4 optic nerves showed no permanent loss of function from 60 min of combined oxygen + glucose withdrawal. Unexpectedly, optic nerves from P21–P49 rats recovered significantly less after all three conditions than adult opticnerves (>P50). It is probable that this period of final myelination corresponds to a time of heightened metabolic activity in white matter. The tolerance of CNS white matter to energy deprivation can be categorized into four stages that are correlated with specific developmental features: premyelination (P0–P4), highly tolerant to anoxia, aglycemia and combined anoxia/aglycemia; early myelination (P5–P20), partially tolerant of anoxia and aglycemia but not to combined anoxia/aglycemia; late myelination (P21–P49), very low tolerance of anoxia, aglycemia and combined anoxia/aglycemia; and mature (>P50), low tolerance of anoxia, aglycemia and combined anoxia/aglycemia. The relative resistance of optic nerve function to glucose withdrawal in the presence of oxygen, compared with glucose withdrawal in the absence of oxygen, is presumably due to the presence of oxygen-dependent energy reserves such as astrocytic glycogen, amino acids. and phospholipids.Keywords
This publication has 69 references indexed in Scilit:
- Hypoglycaemia in the Neonate: How and When Is It Important?Developmental Neuroscience, 1994
- Anoxia-Induced Changes in Extracellular K+and pH in Mammalian Central White MatterJournal of Cerebral Blood Flow & Metabolism, 1992
- Non-synaptic mechanisms of Ca2+-mediated injury in CNS white matterTrends in Neurosciences, 1991
- Simulation of aspects of ischemia in cell culture: Changes in lactate compartmentationGlia, 1990
- Lactate-Supported Synaptic Function in the Rat Hippocampal Slice PreparationScience, 1988
- Hypoglycemia, brain metabolism, and brain damageDiabetes/Metabolism Research and Reviews, 1988
- Lactate release from cultured astrocytes and neurons: A comparisonGlia, 1988
- Rat optic nerve: Electrophysiological, pharmacological and anatomical studies during developmentDevelopmental Brain Research, 1982
- Histochemistry of glycogen deposition in perinatal rat brain: importance of radial glial cellsJournal of Neurocytology, 1981
- Symptomatic neonatal hypoglycemia associated with toxemia of pregnancyThe Journal of Pediatrics, 1959