Fructose Supports Energy Metabolism of Some, But Not All, Axons in Adult Mouse Optic Nerve
Authors:
- Susan AndersonSASusan Anderson
- Paul MeakinPMPaul Meakin
- Bruce R. RansomBRBruce R. Ransom
- Angus M. BrownABAngus M. Brown
- 1 March 2006
- journal article
- research article
- Published by American Physiological Society in Journal of Neurophysiology
- Vol. 95 (3) , 1917-1925
Abstract
We used transmission electron microscopy (TEM) and electrophysiological techniques to characterize the morphology and stimulus-evoked compound action potential (CAP), respectively, of the adult mouse optic nerve (MON). Electrophysiological recordings demonstrated an identical CAP profile for each MON. An initial peak, smallest in area and presumably composed of the fastest-conducting axons displayed the lowest threshold for activation as expected for large axons. The second peak, the largest, was presumably composed of axons of intermediate diameter and conduction velocity, and the third peak was composed of the slowest and presumably smallest axons. In 10 mM fructose, the first CAP peak area was reduced by 78%, but the second and third peaks were unaffected. Histological analysis revealed a cross-sectional area of 33,346 μm2, containing 24,068 axons per MON. All axons were myelinated and axon diameter ranged from 0.09 to 2.58 μm, although 80 ± 6% of the axons were 2 μm in diameter. After bathing in fructose for 2 h 94 ± 2% of normal appearing axons were 1.5 μm—all of the larger axons being grossly abnormal in structure. We conclude that fructose is unable to support function of the larger axons contributing to the first CAP peak, thus enabling us to identify a distinct population of axons that contributes to that peak.Keywords
This publication has 30 references indexed in Scilit:
- Re-establishing the regenerative potential of central nervous system axons in postnatal miceJournal of Cell Science, 2005
- Na+ channel expression along axons in multiple sclerosis and its modelsTrends in Pharmacological Sciences, 2004
- Mice Lacking Sodium Channel β1 Subunits Display Defects in Neuronal Excitability, Sodium Channel Expression, and Nodal ArchitectureThe Journal of Neuroscience, 2004
- Axon Function Persists during Anoxia in Mammalian White MatterJournal of Cerebral Blood Flow & Metabolism, 2003
- Glycogen Regulation and Functional Role in Mouse White MatterThe Journal of Physiology, 2003
- Ionic Mechanisms of Aglycemic Axon Injury in Mammalian Central White MatterJournal of Cerebral Blood Flow & Metabolism, 2001
- Changes of compound action potentials in retrograde axonal degeneration of rat optic nerveExperimental Neurology, 1995
- Macromolecular structure of axon membrane and action potential conduction in myelin deficient and myelin deficient heterozygote rat optic nervesJournal of Neurocytology, 1990
- Postnatal differentiation of rat optic nerve fibers: Electron microscopic observations on the development of nodes of Ranvier and axoglial relationsJournal of Comparative Neurology, 1984
- Strain differences in quantitative analysis of the rat optic nerveExperimental Neurology, 1982