Evaluation of the effects of cocaine, heroin and naltrexone, alone and in combination, on milk drinking in rats.

J. K. Rowlett, W. L. Woolverton

BEHAVIOURAL PHARMACOLOGY(1995)

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摘要
The effects of cocaine, alone and in combination with either heroin or naltrexone, were examined using a milk drinking procedure in rats. Rats (n = 8) were given access to a sweetened milk solution for 15 min daily until intake had stabilized (3 days with less than 10% variation across days). Rats were first administered saline or one of five doses of either cocaine (2.0-32 mg/kg, i.p.) or heroin (0.4-3.2 mg/kg, i.p.) 15 min prior to milk access. The dose-response function for cocaine was then determined in combination with either 0.8 mg/kg or 1.6 mg/kg heroin. Both cocaine and heroin administered alone produced dose-dependent decreases in milk drinking. Combination with 0.8 mg/kg and 1.6 mg/kg heroin resulted in parallel shifts to the left in the cocaine dose-response function. Isobolographic analysis of these dose-response functions using ED(50) and ED(75) values revealed that the combinations of cocaine and heroin were dose-additive, except at the cocaine plus 1.6 mg/kg heroin combination, which was infra-additive. Redetermination of the cocaine-only and heroin-only dose-response functions revealed no significant difference from the first determination. To assess the effects of naltrexone on cocaine- and heroin-induced suppression of milk drinking, rats were first administered four doses of naltrexone (0.1-0.8 mg/kg, i.p., 15 min pretreatment). Then, naltrexone doses were combined with a dose of heroin or cocaine that suppressed milk drinking (3.2 and 16 mg/kg, respectively), Naltrexone alone produced modest, but not dose-related, suppression of milk drinking, and had no reliable effect on suppression of milk drinking produced by 16 mg/kg cocaine. In contrast, naltrexone dose-dependently blocked heroin-induced suppression of milk drinking and, at naltrexone doses that had no effect on milk drinking when administered alone, produced a parallel shift to the right in the heroin dose-response function. In vivo apparent pK(B) analyses revealed that naltrexone antagonism of heroin-induced suppression of milk drinking involved mu-opioid receptors. Taken together, these results suggest that the effects of cocaine and heroin on milk drinking are either dose-additive or infra-additive and that cocaine-induced suppression of milk drinking does not directly involve the mu-opioid receptor system.
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关键词
cocaine,heroin,isobologram,pK(B) analysis,polydrug abuse,rat,speedball
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