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Chronic systemic injection of D-galactose impairs the septohippocampal cholinergic system in rats.

Abstract
Accumulated evidence indicates chronic systemic injection of D-galactose mimics aging progress induced by oxidative stress. We addressed whether memory impairment in this model was associated with the cholinergic septohippocampal degeneration. Rats injected with D-galactose for 6 weeks showed impairment of spatial learning and memory as measured by the water maze test. Correspondingly, anti-choline acetyltransferase immunohistochemistry demonstrated a severe loss of cholinergic terminals in the hippocampus accompanied by a mild cholinergic neuronal atrophy and loss in the medial septum and the nucleus of the vertical limb of the diagonal band of Broca. A major synaptic degeneration in the hippocampus was confirmed by ultrastructural analysis. These findings provide neuropathological evidence for rodents with chronic injection of D-galactose as a promising model for brain aging and age-related neurodegeneration.
AuthorsMing Lei, Yang Su, Xiangdong Hua, Jiong Ding, Qunying Han, Gang Hu, Ming Xiao
JournalNeuroreport (Neuroreport) Vol. 19 Issue 16 Pg. 1611-5 (Oct 29 2008) ISSN: 1473-558X [Electronic] England
PMID18845941 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Choline O-Acetyltransferase
  • Galactose
Topics
  • Aging (physiology)
  • Animals
  • Behavior, Animal (drug effects, physiology)
  • Choline O-Acetyltransferase (genetics, metabolism)
  • Galactose (administration & dosage, toxicity)
  • Hippocampus (drug effects, metabolism, pathology)
  • Immunohistochemistry
  • Injections, Subcutaneous
  • Male
  • Maze Learning (drug effects, physiology)
  • Memory (drug effects, physiology)
  • Microscopy, Electron
  • Nerve Degeneration (chemically induced, physiopathology)
  • Neurons (drug effects, metabolism, pathology)
  • Rats
  • Rats, Sprague-Dawley
  • Septal Nuclei (drug effects, metabolism, pathology)
  • Spatial Behavior (drug effects, physiology)
  • Synapses (drug effects, physiology, ultrastructure)

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