GABAA receptors in the mediodorsal thalamus play a crucial role in rat shell-specific acetylcholine-mediated,but not dopamine-mediated,turning behaviour |
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Authors: | H Ikeda A Kotani J Lee N Koshikawa AR Cools |
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Institution: | 1. Department of Pharmacology, Nihon University School of Dentistry, 1-8-13 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan;2. Dental Research Centre, Nihon University School of Dentistry, 1-8-13 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan;3. Department of Complete Denture Prosthodontics, Nihon University School of Dentistry, 1-8-13 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan;4. Department of Cognitive Neurosciences, Psychoneuropharmacology, Radboud University of Nijmegen, PO Box 9101, 6500 HB Nijmegen, The Netherlands |
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Abstract: | The role of GABAA receptors in the mediodorsal thalamus (mdT) in turning behaviour of rats was studied. Neither the GABAA receptor agonist muscimol (50 ng) nor the antagonist bicuculline (200 ng) unilaterally injected into the mdT elicited any behavioural change. Unilateral injection of the acetylcholine receptor agonist (carbachol, 5 μg) into the nucleus accumbens shell has been found to elicit contraversive circling while unilateral injection of a mixture of dopamine D1 ((±)-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol SKF 38393], 5 μg) and D2 (quinpirole, 10 μg) receptor agonists into the same site is known to elicit contraversive pivoting. The contraversive circling induced by unilateral injection of carbachol (5 μg) into the nucleus accumbens shell was dose-dependently inhibited by muscimol (25 and 50 ng) injected into the mdT. This inhibitory effect of muscimol (50 ng) was antagonised by co-administration of bicuculline (200 ng), which alone did not modify the contraversive circling induced by carbachol (5 μg). The contraversive pivoting induced by unilateral injection of a mixture of SKF 38393 (5 μg) and quinpirole (10 μg) into the nucleus accumbens shell was inhibited by muscimol (25 and 50 ng) injected into the mdT, whereas bicuculline (200 ng) injected into the mdT did not significantly modify the pivoting. The inhibitory effect of muscimol (50 ng) on the pivoting induced by a mixture of SKF 38393 (5 μg) and quinpirole (10 μg) was not dose-dependent and not antagonised by bicuculline (200 ng). The present study suggests that GABAA receptors in the mdT play a limited role in spontaneously occurring locomotor activity. Secondly, this study demonstrates that GABAA receptors in the mdT transmit accumbens-dependent cholinergic circling, but not accumbens-dependent dopaminergic pivoting, to other brain structures. Finally, the present study shows that muscimol-sensitive, non-GABAA receptors in the mdT influence the accumbens-dependent dopaminergic pivoting. To what extent GABAB receptors in the mdT mediate the muscimol-induced effects upon the dopaminergic pivoting behaviour requires additional research. |
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Keywords: | acetylcholine dopamine GABA nucleus accumbens mediodorsal thalamus rat |
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