BEHAVIORAL-EFFECTS OF (+ -)-1-(2,5-DIMETHOXY-4-IODOPHENYL)-2-AMINOPROPANE, (DOI) IN THE ELEVATED PLUS-MAZE TEST/

Citation
Es. Onaivi et al., BEHAVIORAL-EFFECTS OF (+ -)-1-(2,5-DIMETHOXY-4-IODOPHENYL)-2-AMINOPROPANE, (DOI) IN THE ELEVATED PLUS-MAZE TEST/, Life sciences, 57(26), 1995, pp. 2455-2466
Citations number
42
Categorie Soggetti
Biology,"Medicine, Research & Experimental","Pharmacology & Pharmacy
Journal title
ISSN journal
00243205
Volume
57
Issue
26
Year of publication
1995
Pages
2455 - 2466
Database
ISI
SICI code
0024-3205(1995)57:26<2455:BO(->2.0.ZU;2-F
Abstract
The serotonin (5-hydroxytryptamine, 5-HT) system has consistently been implicated in the actions of +/-)-1-(2,5-dimethoxy-4-iodophenyl)-2-am inopropane (DOI) and other hallucinogens. Recent evidence suggest that the 5-HT2A/2C receptor subtypes may be major targets for such drugs i n the CNS. DOI-treated hooded rats (0.1-5.0 mg/kg) and DOI treated ICR mice (0.1-2.0 mg/kg), displayed aversions at lower doses and anti-ave rsions at higher doses to the open arms of the plus-maze. Mianserin (0 .5 mg/kg) and ketanserin (0.1 mg/kg) blocked the anti-aversive behavio r, but only mianserin was effective at reversing the aversions produce d by the higher doses of DOI in the ICR mice. DOI produced an intense aversion in the DBA/2 and anti-aversion in the C57/BL6 mice to the ope n arms of the plus-maze. These opposing actions of DOI in the plus-maz e may be exploited in studying the neurobehavioral effects of hallucin ogens. Since flumazenil was ineffective at blocking the DOI induced ch anges, it was concluded that the mechanism of DOI induced anxiolysis o r anxiogenesis may not involve an action at the benzodiazepine recepto rs.