Neuromotor alterations and cerebellar deficits in aged arylsulfatase A-deficient transgenic mice

Neurosci Lett. 1999 Oct 1;273(2):93-6. doi: 10.1016/s0304-3940(99)00647-3.

Abstract

Arylsulfatase A (ASA)-deficient (-/-) mice and ASA(+/+) controls were constructed as a transgenic model for the lysosomal storage disease, metachromatic leukodystrophy (MLD). One-year-old ASA(-/-) mice showed impaired rotarod performance and altered walking pattern characterized by a shorter pace, later evolving into more severe ataxia with tremor in 2-year-old mice. Examination of cerebellar histology showed that 2-year-old ASA(-/-) mice have lost most of the calbindin immunoreactivity from their Purkinje cell dendrites and show simplified dendritic architecture. Additionally, ASA-deficient mice lost a substantial proportion of their Purkinje cells. Recordings of unitary potentials and stimulation of climbing fibers on cerebellar slices from 2-year-old mice indicated that, although the main cerebellar synapses seem to be present and functioning physiologically, the climbing fibers of ASA-deficient mice may have enhanced effects on Purkinje cell activity. It is concluded that ambulatory dysfunctions in ASA(-/-) mice might be explained by an imbalance in the consequences of climbing fiber signals upon Purkinje cell activity due to selective neurodegeneration within the cerebellum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / physiology*
  • Animals
  • Calbindins
  • Cerebellar Diseases / etiology*
  • Cerebellar Diseases / metabolism
  • Cerebellar Diseases / pathology
  • Cerebellum / metabolism
  • Cerebroside-Sulfatase / deficiency*
  • Cerebroside-Sulfatase / genetics
  • Dendrites / metabolism
  • Electric Stimulation
  • Electrophysiology
  • Female
  • In Vitro Techniques
  • Leukodystrophy, Metachromatic / genetics
  • Leukodystrophy, Metachromatic / pathology
  • Leukodystrophy, Metachromatic / physiopathology
  • Mice
  • Mice, Transgenic / genetics
  • Motor Activity
  • Psychomotor Performance*
  • Purkinje Cells / metabolism
  • Purkinje Cells / pathology
  • S100 Calcium Binding Protein G / metabolism

Substances

  • Calbindins
  • S100 Calcium Binding Protein G
  • Cerebroside-Sulfatase