Traumatic brain injury reduces hippocampal high-affinity [3H]choline uptake but not extracellular choline levels in rats

Neurosci Lett. 1994 Oct 24;180(2):127-30. doi: 10.1016/0304-3940(94)90503-7.

Abstract

Hippocampal cholinergic hypofunction may contribute to memory deficits following experimental traumatic brain injury. These studies examined two important factors in acetylcholine synthesis: choline availability and neuronal uptake. No reductions in basal extracellular choline levels, using microdialysis, were observed 2 weeks after cortical impact injury. However, studies of high affinity [3H]choline uptake in the hippocampus, measured in a synaptosomal preparation, found a reduction in the maximum velocity of choline uptake (Vmax), while no differences in affinity constants (Km) were found. The results suggest that post-traumatic cholinergic deficits are not attributable to decreased availability of choline, but may be associated with either a decreased ability of cholinergic neurons to take up choline and/or a loss of cholinergic neurons.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetylcholine / biosynthesis
  • Animals
  • Biological Transport
  • Brain Injuries / metabolism*
  • Brain Injuries / psychology
  • Choline / pharmacokinetics*
  • Craniotomy
  • Extracellular Space / metabolism
  • Hippocampus / metabolism*
  • Memory Disorders / etiology
  • Memory Disorders / physiopathology
  • Microdialysis
  • Neurons / metabolism
  • Rats
  • Wounds, Nonpenetrating / metabolism
  • Wounds, Nonpenetrating / psychology

Substances

  • Choline
  • Acetylcholine