Deficits induced by quinolinic acid lesion to the striatum in a position discrimination and reversal task are ameliorated by permanent and temporary lesion to the globus pallidus: a potential novel treatment in a rat model of Huntington's disease.

Abstract

Symptoms in the early stages of Huntington's disease (HD) are assumed to reflect basal ganglia circuit dysfunction secondary to degeneration of striatal projections to the external segment of the globus pallidus (GPe). The hypothesis that GPe lesion would ameliorate HD symptoms by "normalizing" the circuit's functioning was tested in a rat model of this disease. The performance of rats sustaining quinolinic acid lesion to the striatum (a rat model of HD) in a position discrimination and reversal task was compared with the performance of rats sustaining in addition a bilateral excitotoxic lesion to the globus pallidus (GP) carried out simultaneously with the striatal lesion (Experiment 1) or 1 month after the striatal lesion (Experiment 2), as well as a unilateral temporary lesion of the GP (Experiment 3). The striatal lesion-induced deficit in the task was effectively reversed by a bilateral excitotoxic GP lesion carried out simultaneously or 1 month after the striatal lesion, as well as by a temporary unilateral GP inactivation. Given that a similar dysfunction of basal ganglia circuitry is thought to subserve the behavioral alterations seen in quinolinic acid lesioned rats and some of the symptoms in HD, these results raise the possibility that lesion or inactivation of the GPe may alleviate some of HD symptoms.

• Authors: Daphna Joel, Liat Ayalon, Ricardo Tarrasch, Ina Weiner
• Journal: Movement disorders : official journal of the Movement Disorder Society (Mov Disord) Vol. 18 Issue 12 Pg. 1499-507 (Dec 2003) ISSN: 0885-3185 [Print] United States
• PMID: 14673887 (Publication Type: Evaluation Study, Journal Article)
• Copyright: Copyright 2003 Movement Disorder Society

Chemical References

• Quinolinic Acid

Topics

• Animals
• Basal Ganglia (drug effects, physiopathology)
• Corpus Striatum (drug effects, pathology)
• Discrimination Learning (drug effects)
• Disease Models, Animal
• Female
• Globus Pallidus (drug effects, pathology)
• Huntington Disease (drug therapy, pathology, physiopathology)
• Injections
• Male
• Nerve Net (drug effects, pathology)
• Quinolinic Acid (administration & dosage, adverse effects)
• Random Allocation
• Rats
• Rats, Wistar