EFFECTS OF ALPHA-ADRENOCEPTOR AGONISTS AND ANTAGONISTS IN A MAZE-EXPLORATION MODEL OF FEAR-MOTIVATED BEHAVIOR
EFFECTS OF ALPHA-ADRENOCEPTOR AGONISTS AND ANTAGONISTS IN A MAZE-EXPLORATION MODEL OF FEAR-MOTIVATED BEHAVIOR
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DOI:
10.1007/bf00504983
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发表时间:
1984-01-01
影响因子:
3.6
通讯作者:
MITHANI, S
中科院分区:
文献类型:
--
作者:
HANDLEY, SL;MITHANI, S
An elevated X-maze with alternating open and enclosed arms was investigated as a fear-induced behavior model. Anxiolytics (diazepam and amylobarbitone) increased and putative anxiogenics (ACTH and picrotoxin) decreased the proportion of open arm entries. The .alpha.1-adrenoceptor agonists, phenylephrine and ST587 (2-(2-chloro-5-trifluoromethylphenylimino)imidazolidine), and the .alpha.2-adrenoceptor antagonists, idazoxan, piperoxane, RS-21361 [2-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]-1-ethyl-1H-imidazole] and yohimbine, decreased relative open-arm entries, resembling the putative anxiogenics. Azepexole, clonidine and guanabenz, .alpha.2-adrenoceptor agonists, and the .alpha.1-adrenoceptor antagonists, prazosin and thymoxamine, enhanced the proportion of open arm entries at low doses, suggesting anxiolytic-like properties. A paradoxical fall in open arm entries occurred with these agents at higher doses. The involvement of noradrenergic systems in fear-motivated behavior was shown.