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Comparison of naltrexone and quaternary naltrexone after systemic and intracerebroventricular administration in pigeons

机译:纳米曲酮和季甲酮在鸽子中的颅内神经施用后的比较

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摘要

The behavioral effects of naltrexone and quaternary naltrexone were evaluated in two groups of pigeons. One group responded under a fixed-ratio schedule of food reinforcement and was trained to discriminate between 3.2 mg/kg morphine (i.m.) and saline. Drug-appropriate responding occurred in a dose-related manner to morphine, given intramuscularly and intraventricularly. When administered intraventricularly morphine was 50 times more potent as a discriminative stimulus and 50-100 times more potent at suppressing responding. Naltrexone, given intraventricularly and intramuscularly, attenuated the discriminative stimulus effects of morphine. Quaternary naltrexone was more potent at suppressing responding when administered intraventricularly but it failed to attenuate the discriminative stimulus effects of morphine. A second group of pigeons, responding under a variable-interval schedule of food reinforcement, was treated with 100.0 mg/kg/day of morphine. Naltrexone and quaternary naltrexone suppressed responding by both routes of administration. Naltrexone was approximately equipotent when given intramuscularly or intraventricularly, and the doses that suppressed responding were 50-500 times smaller than doses required to suppress responding in untreated pigeons. Although quaternary naltrexone was 1800 times more potent when given intraventricularly, the doses necessary to suppress responding by each route were the same as doses required in untreated pigeons. These results extend the conditions under which a quaternary derivative of naltrexone failed to display antagonist activity in the pigeon. The utility of this compound for characterizing central and peripheral mechanisms of action has not been established in different species and testing conditions and, therefore, appears to be appropriate only under conditions in which it is evaluated after systemic, as well as central, administration.
机译:在两组鸽子中评价了纳曲酮和季甲醛酮的行为效应。一组根据食品增强的定义计划响应,培训以区分3.2mg / kg吗啡(即)和盐水。药物适当的响应以与肌内和静脉内的剂量相关的方式发生给吗啡。当静脉内施用时,随着鉴别的刺激,当鉴别刺激的含量是50倍,抑制响应的效率更高50-100倍。纳伦酮,静脉内和肌肉内鉴定,抑制了吗啡的鉴别刺激作用。在静脉内施用时抑制响应时季纳曲酮更有效,但未衰减吗啡的鉴别刺激作用。第二组鸽子,在食物增强的可变间隔时间表中响应,用100.0mg / kg /天吗啡治疗。 NALTREXONE和第四族纳曲酮通过管理途径抑制响应。当肌内或静脉内或静脉内或静脉内或抑制响应的剂量比抑制未处理的鸽子抑制响应的剂量小于50-500倍的剂量,纳曲酮近似等待。虽然在静脉内给予时季纳曲酮是1800倍的效力,但每条途径抑制响应所需的剂量与未处理鸽子所需的剂量相同。这些结果延长了纳曲酮的季衍生物未能在鸽子中显示拮抗剂活性的条件。该化合物用于表征中央和外周动作机制的效用尚未在不同的物种和测试条件下建立,因此,似乎仅适当在系统性和中央管理后评估的条件下。

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