TY - JOUR
T1 - Activity modulation of the globus pallidus and the nucleus entopeduncularis affects compulsive checking in rats
AU - Djodari-Irani, Anaïs
AU - Klein, Julia
AU - Banzhaf, Johann
AU - Joel, Daphna
AU - Heinz, Andreas
AU - Harnack, Daniel
AU - Lagemann, Tobias
AU - Juckel, Georg
AU - Kupsch, Andreas
AU - Morgenstern, Rudolf
AU - Winter, Christine
N1 - Funding Information: We wish to thank C. Koelske and R. Winter for their excellent technical assistance. The study was supported by GIF grant ( 851/2004 ).
PY - 2011/5/16
Y1 - 2011/5/16
N2 - Deep brain stimulation at high frequencies (HFS) is currently studied in the treatment of therapy-refractory obsessive-compulsive disorder (OCD). The diversity of targeted brain areas and the discrepancy in demonstrating beneficial effects, highlight the need for better mapping of brain regions in which HFS may yield anti-compulsive effects. This goal may be achieved by investigating the effects of HFS in appropriate animal models of OCD. The present study tested the effect of bilateral HFS or pharmacological inactivation (as induced by intracerebral administration of the GABA-agonist muscimol) of both the Globus pallidus (GP; rodent equivalent to human GP externus) and the Nucleus entopeduncularis (EP; rodent equivalent to human GP internus) on checking behaviour in the quinpirole rat model of OCD. We demonstrate that HFS of the GP does not and HFS of the EP only partially reduces OCD-like behaviour in rats. In contrast, pharmacological inactivation of both GP and EP significantly reduces OCD-like behaviour in the model. These data contrast previously derived data on the effectiveness of HFS of the subthalamic nucleus, nucleus accumbens, GP and EP in the same and other rat models of OCD. We conclude that (i) although GP and EP play an important role in the pathophysiology of OCD, these areas may not represent first choice target structures for HFS, (ii) the effectiveness of HFS may depend on different subtypes of OCD, represented in different animal models, and (iii) differential net mechanisms may subserve the effectiveness of HFS and pharmacological inactivation.
AB - Deep brain stimulation at high frequencies (HFS) is currently studied in the treatment of therapy-refractory obsessive-compulsive disorder (OCD). The diversity of targeted brain areas and the discrepancy in demonstrating beneficial effects, highlight the need for better mapping of brain regions in which HFS may yield anti-compulsive effects. This goal may be achieved by investigating the effects of HFS in appropriate animal models of OCD. The present study tested the effect of bilateral HFS or pharmacological inactivation (as induced by intracerebral administration of the GABA-agonist muscimol) of both the Globus pallidus (GP; rodent equivalent to human GP externus) and the Nucleus entopeduncularis (EP; rodent equivalent to human GP internus) on checking behaviour in the quinpirole rat model of OCD. We demonstrate that HFS of the GP does not and HFS of the EP only partially reduces OCD-like behaviour in rats. In contrast, pharmacological inactivation of both GP and EP significantly reduces OCD-like behaviour in the model. These data contrast previously derived data on the effectiveness of HFS of the subthalamic nucleus, nucleus accumbens, GP and EP in the same and other rat models of OCD. We conclude that (i) although GP and EP play an important role in the pathophysiology of OCD, these areas may not represent first choice target structures for HFS, (ii) the effectiveness of HFS may depend on different subtypes of OCD, represented in different animal models, and (iii) differential net mechanisms may subserve the effectiveness of HFS and pharmacological inactivation.
KW - Deep brain stimulation
KW - Muscimol
KW - Obsessive-compulsive disorder
KW - Quinpirole
UR - http://www.scopus.com/inward/record.url?scp=79251557170&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.bbr.2010.12.036
DO - https://doi.org/10.1016/j.bbr.2010.12.036
M3 - مقالة
SN - 0166-4328
VL - 219
SP - 149
EP - 158
JO - Behavioural Brain Research
JF - Behavioural Brain Research
IS - 1
ER -