TY - JOUR
T1 - Partial dopaminergic denervation-induced impairment in stimulus discrimination acquisition in parkinsonian rats
T2 - A model for early Parkinson's disease
AU - Eagle, Andrew L.
AU - Olumolade, Oluyemi O.
AU - Otani, Hajime
N1 - Funding Information:
This study was jointly supported by the Neuroscience Program and the Department of Psychology at Central Michigan University . This project also received support from the College of Graduate Studies, the College of Humanities and Social and Behavioral Sciences, and the undergraduate Student Research and Creative Endeavors Exhibition grant at Central Michigan University. The authors would also like to acknowledge the significant contribution of Dr. Justin Oh-Lee to this manuscript.
Publisher Copyright:
© 2014 Elsevier Ireland Ltd and the Japan Neuroscience Society.
PY - 2015/3/1
Y1 - 2015/3/1
N2 - Parkinson's disease (PD) produces progressive nigrostriatal dopamine (DA) denervation resulting in cognitive and motor impairment. However, it is unknown whether cognitive impairments, such as instrumental learning deficits, are associated with the early stage PD-induced mild DA denervation. The current study sought to model early PD-induced instrumental learning impairments by assessing the effects of low dose (5.5μg), bilateral 6OHDA-induced striatal DA denervation on acquisition of instrumental stimulus discrimination in rats. 6OHDA (n=20) or sham (n=10) lesioned rats were tested for stimulus discrimination acquisition either 1 or 2 weeks post surgical lesion. Stimulus discrimination acquisition across 10 daily sessions was used to assess discriminative accuracy, or a probability measure of the shift toward reinforced responding under one stimulus condition (Sd) away from extinction, when reinforcement was withheld, under another (Sd phase). Striatal DA denervation was assayed by tyrosine hydroxylase (TH) staining intensity. Results indicated that 6OHDA lesions produced significant loss of dorsal striatal TH staining intensity and marked impairment in discrimination acquisition, without inducing akinetic motor deficits. Rather 6OHDA-induced impairment was associated with perseveration during extinction (Sδ phase). These findings suggest that partial, bilateral striatal DA denervation produces instrumental learning deficits, prior to the onset of gross motor impairment, and suggest that the current model is useful for investigating mild nigrostriatal DA denervation associated with early stage clinical PD.
AB - Parkinson's disease (PD) produces progressive nigrostriatal dopamine (DA) denervation resulting in cognitive and motor impairment. However, it is unknown whether cognitive impairments, such as instrumental learning deficits, are associated with the early stage PD-induced mild DA denervation. The current study sought to model early PD-induced instrumental learning impairments by assessing the effects of low dose (5.5μg), bilateral 6OHDA-induced striatal DA denervation on acquisition of instrumental stimulus discrimination in rats. 6OHDA (n=20) or sham (n=10) lesioned rats were tested for stimulus discrimination acquisition either 1 or 2 weeks post surgical lesion. Stimulus discrimination acquisition across 10 daily sessions was used to assess discriminative accuracy, or a probability measure of the shift toward reinforced responding under one stimulus condition (Sd) away from extinction, when reinforcement was withheld, under another (Sd phase). Striatal DA denervation was assayed by tyrosine hydroxylase (TH) staining intensity. Results indicated that 6OHDA lesions produced significant loss of dorsal striatal TH staining intensity and marked impairment in discrimination acquisition, without inducing akinetic motor deficits. Rather 6OHDA-induced impairment was associated with perseveration during extinction (Sδ phase). These findings suggest that partial, bilateral striatal DA denervation produces instrumental learning deficits, prior to the onset of gross motor impairment, and suggest that the current model is useful for investigating mild nigrostriatal DA denervation associated with early stage clinical PD.
KW - 6-Hydroxydopamine
KW - Discrimination
KW - Dopamine
KW - Dorsal striatum
KW - Extinction
KW - Parkinson's disease
UR - http://www.scopus.com/inward/record.url?scp=84923617748&partnerID=8YFLogxK
U2 - 10.1016/j.neures.2014.11.002
DO - 10.1016/j.neures.2014.11.002
M3 - Article
C2 - 25452126
AN - SCOPUS:84923617748
SN - 0168-0102
VL - 92
SP - 71
EP - 79
JO - Neuroscience Research
JF - Neuroscience Research
ER -