| Literature DB >> 7151866 |
B Costall, J F Eniojukan, R J Naylor.
Abstract
Measurement of spontaneous climbing behaviour of mice, made in Mouse Climbing Monitors which used photocell detection of vertical movements, was most reliable and intense when made over a 40 min period using two mice per cage and taking readings before 2:00 p.m. The climbing response was antagonised by low doses of the neuroleptics (-)-sulpiride and spiroperidol, and by low doses of the dopamine agonists apomorphine, N-n-propylbenzo(f)quinoline, N-n-propylbenzo(g)quinoline and 2-di-n-propylamino-5,6-dihydroxytetralin; N,N-dipropyldopamine was less effective. Higher doses of the dopamine agonists induced climbing. The inhibition afforded by apomorphine was partially antagonised by (-)-sulpiride and spiroperidol (at doses which do not in themselves modify spontaneous climbing) but not by prazosin or yohimbine. Bilateral electrolesions of the caudate-putamen, nucleus accumbens or tuberculum olfactorium attenuated spontaneous climbing for the first 5-9 postoperative days, the accumbens lesions being most effective. Thus, spontaneous climbing behaviour of mice can be precisely quantified, dopamine-containing forebrain areas are involved with its expression and it can be potently modified by dopamine agonists and antagonists.Entities:
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Year: 1982 PMID: 7151866 DOI: 10.1016/0014-2999(82)90457-5
Source DB: PubMed Journal: Eur J Pharmacol ISSN: 0014-2999 Impact factor: 4.432