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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >Reinstatement of cocaine-seeking behavior in rats is attenuated following repeated treatment with the opioid receptor antagonist naltrexone.
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Reinstatement of cocaine-seeking behavior in rats is attenuated following repeated treatment with the opioid receptor antagonist naltrexone.

机译:用阿片受体拮抗剂纳曲酮反复治疗后,大鼠可卡因寻求行为的恢复减弱。

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In the present study we show that the endogenous opioid systems play a modulating role in cocaine-induced reinstatement of drug-seeking behavior in rats. We investigated the effect of blockade of opioid receptors on reinstatement of cocaine-seeking behavior by cocaine priming. Drug-naive rats were allowed to initiate self-administration behavior of cocaine (30 and 60 mug per infusion, i.v.) for 5 consecutive daily sessions, and after a 5-day extinction period during which the rats did not receive cocaine, a test for cocaine-induced (1 mg/kg, i.v.) reinstatement followed. The effect of cocaine priming was tested on days 1, 3, and 5 after extinction, while on days 2 and 4 the animals received saline priming. Before each daily reinstatement test, different groups of animals received an injection with the opioid receptor antagonist naltrexone (3 mg/kg, s.c.) or with placebo. We observed that cocaine readily reinstated extinguished responding in the rats, and that this reinstatement responding did not change over the consecutive reinstatement tests. Pretreatment with naltrexone progressively attenuates the cocaine-induced reinstatement, with a significant reduction on days 3 and 5 of reinstatement testing. Discriminative lever-pressing (active versus inactive lever) during reinstatement phase, however, remains present in animals treated with naltrexone. This implies that repeated opioid receptor blockade progressively attenuates cocaine-induced drug-seeking behavior in abstained animals, but this cannot simply be attributed to extinction of cocaine-seeking behavior.
机译:在本研究中,我们表明内源性阿片样物质系统在可卡因诱导的大鼠寻药行为的恢复中起调节作用。我们调查了可卡因引发引发的阿片受体阻滞对恢复可卡因寻求行为的影响。允许未吸毒的大鼠连续5天每天开始可卡因的自我给药行为(每次输注30和60杯,iv),并且在灭绝5天后大鼠没有接受可卡因的情况下进行自我测试,随后是可卡因诱导的(1 mg / kg,iv)恢复。在灭绝后的第1、3和5天测试可卡因引发的效果,而在第2天和第4天,动物接受盐水引发。在每次每日恢复测试之前,不同组的动物接受阿片受体拮抗剂纳曲酮(3 mg / kg,皮下注射)或安慰剂注射。我们观察到可卡因在大鼠中很容易恢复熄灭的反应,并且在连续的恢复试验中,这种恢复反应没有改变。纳曲酮预处理可逐渐减弱可卡因诱导的恢复,并在恢复测试的第3天和第5天显着减少。然而,在恢复阶段,歧视性的杠杆按压(主动杠杆与非主动杠杆)仍然存在于用纳曲酮治疗的动物中。这意味着反复的阿片受体阻滞剂逐渐减弱了可卡因诱导的戒毒动物的药物寻求行为,但这不能简单地归因于可卡因寻求行为的灭绝。

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