Myers W D, Ng K T, Singer G
Physiol Behav. 1984 Sep;33(3):449-55. doi: 10.1016/0031-9384(84)90168-9.
Rats can be induced to self-inject acetaldehyde under an appropriate operant conditioning schedule. The narcotic antagonist naloxone (30 mg/kg) is shown to produce a decrease in schedule-induced acetaldehyde self-injection, but was without effect on both barpress responding and spontaneous activity in rats tested individually for fine, gross and total activity. On the other hand buprenorphine (0.3 and 3 mg/kg), the mixed agonist-antagonist derived from the opium alkaloid thebaine, also produced a significant decrease in acetaldehyde self-injection. However, a significant effect of buprenorphine on barpressing in otherwise drug naive rats indicated that this finding should not be dissociated from a possible involvement of buprenorphine on motor responding. While the findings are consistent with the hypothesis of opiate involvement in acetaldehyde self-administration, caution must be exercised when drawing conclusions about the participation of endogenous opiates in acetaldehyde-mediated behavior.
在适当的操作性条件反射程序下,可诱导大鼠自我注射乙醛。麻醉拮抗剂纳洛酮(30毫克/千克)可使程序诱导的乙醛自我注射减少,但对单独测试精细、总体和总活动的大鼠的压杆反应和自发活动均无影响。另一方面,源自鸦片生物碱蒂巴因的混合激动剂-拮抗剂丁丙诺啡(0.3和3毫克/千克)也可使乙醛自我注射显著减少。然而,丁丙诺啡对原本未接触过药物的大鼠的压杆行为有显著影响,这表明这一发现不应脱离丁丙诺啡可能对运动反应的影响。虽然这些发现与阿片类物质参与乙醛自我给药的假设一致,但在得出内源性阿片类物质参与乙醛介导行为的结论时必须谨慎。