|  Help  |  About  |  Contact Us

Publication : Impairment of reward-related learning by cholinergic cell ablation in the striatum.

First Author  Kitabatake Y Year  2003
Journal  Proc Natl Acad Sci U S A Volume  100
Issue  13 Pages  7965-70
PubMed ID  12802017 Mgi Jnum  J:256660
Mgi Id  MGI:6116748 Doi  10.1073/pnas.1032899100
Citation  Kitabatake Y, et al. (2003) Impairment of reward-related learning by cholinergic cell ablation in the striatum. Proc Natl Acad Sci U S A 100(13):7965-70
abstractText  The striatum in the basal ganglia-thalamocortical circuitry is a key neural substrate that is implicated in motor balance and procedural learning. The projection neurons in the striatum are dynamically modulated by nigrostriatal dopaminergic input and intrastriatal cholinergic input. The role of intrastriatal acetylcholine (ACh) in learning behaviors, however, remains to be fully clarified. In this investigation, we examine the involvement of intrastriatal ACh in different categories of learning by selectively ablating the striatal cholinergic neurons with use of immunotoxin-mediated cell targeting. We show that selective ablation of cholinergic neurons in the striatum impairs procedural learning in the tone-cued T-maze memory task. Spatial delayed alternation in the T-maze learning test is also impaired by cholinergic cell elimination. In contrast, the deficit in striatal ACh transmission has no effect on motor learning in the rota-rod test or spatial learning in the Morris water-maze test or on contextual- and tone-cued conditioning fear responses. We also report that cholinergic cell elimination adaptively up-regulates nicotinic ACh receptors not only within the striatum but also in the cerebral cortex and substantia nigra. The present investigation indicates that cholinergic modulation in the local striatal circuit plays a pivotal role in regulation of neural circuitry involving reward-related procedural learning and working memory.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

3 Bio Entities

Trail: Publication

0 Expression