Department of Drug Sciences, University of Sassari, Via Muroni 23, Sassari, Italy.
Alcohol. 2011 Dec;45(8):773-83. doi: 10.1016/j.alcohol.2011.06.003. Epub 2011 Jul 31.
We have previously shown that acetaldehyde (ACD), the first metabolite of ethanol, regulates its motivational properties and possesses reinforcing effects by itself. A large and still growing body of evidence indicates that the endogenous opioidergic system plays a critical role in the motivational effects of ethanol and suggests a role for extracellular signal-regulated kinase (ERK) in these effects of both ethanol and ACD. The present study was undertaken to examine if opioid-mediated mechanisms are involved in the reinforcing properties of ACD and in ACD-elicited ERK activation. To this end, Wistar rats were trained to orally self-administer ACD (0.2%) by nose poking. Responses on active nose poke caused delivery of ACD solution, whereas responses on inactive nose poke had no consequences. The effect of pretreatment with a nonselective opioid receptor antagonist, naltrexone (NTX), was evaluated during (1) maintenance of ACD self-administration, (2) deprivation effect after ACD extinction, and (3) ACD self-administration under a progressive-ratio schedule of reinforcement. Additionally, we tested the effect of NTX on saccharin (0.05%) reinforcement, as assessed by oral self-administration, and on ACD-elicited ERK phosphorylation in the nucleus accumbens (Acb), as assessed by immunohistochemistry. Finally, we examined the effect of a μ(1)-selective opioid receptor antagonist, naloxonazine (NLZ), on the maintenance phase of ACD and saccharin self-administration. The results indicate that NTX (0.4-0.8mg/kg) reduced the maintenance, the deprivation effect, and the break points of ACD self-administration without suppressing saccharin self-administration. Moreover, NTX decreased ACD-elicited ERK activation in the Acb shell and core. NLZ (10-15mg/kg) reduced the maintenance phase of ACD self-administration without interfering with saccharin self-administration, whereas both NTX and NLZ failed to modify responses on inactive nose poke indicating the lack of a nonspecific behavioral activation. Overall, these results indicate that the opioid system is implicated in the reinforcing properties of ACD and suggest an involvement of ERK. The finding that NTX and NLZ reduce ACD but not saccharin self-administration indicates that these effects are specific to ACD.
我们之前已经表明,乙醇的第一代谢产物乙醛(ACD)通过自身调节其动机特性并具有强化作用。大量且不断增加的证据表明,内源性阿片样物质系统在乙醇的动机作用中起着关键作用,并表明细胞外信号调节激酶(ERK)在乙醇和 ACD 的这些作用中起作用。本研究旨在检查阿片介导的机制是否参与 ACD 的强化特性以及 ACD 诱导的 ERK 激活。为此,通过鼻探训练 Wistar 大鼠口服自我给予 ACD(0.2%)。主动鼻探引起 ACD 溶液的输送,而被动鼻探没有后果。在(1)ACD 自我给药维持期间、(2)ACD 消退后的剥夺效应期间和(3)递增比例强化方案下的 ACD 自我给药期间,评估了非选择性阿片受体拮抗剂纳曲酮(NTX)预处理的效果。此外,我们测试了 NTX 对蔗糖(0.05%)强化的影响,通过口服自我给药评估,以及对核 Accumbens(Acb)中 ACD 诱导的 ERK 磷酸化的影响,通过免疫组织化学评估。最后,我们检查了 μ(1)-选择性阿片受体拮抗剂纳洛酮嗪(NLZ)对 ACD 和蔗糖自我给药维持阶段的影响。结果表明,NTX(0.4-0.8mg/kg)降低了 ACD 自我给药的维持、剥夺效应和断点,而不抑制蔗糖自我给药。此外,NTX 降低了 Acb 壳和核中 ACD 诱导的 ERK 激活。NLZ(10-15mg/kg)降低了 ACD 自我给药的维持阶段,而不干扰蔗糖自我给药,而 NTX 和 NLZ 均未能改变被动鼻探的反应,表明缺乏非特异性行为激活。总体而言,这些结果表明阿片系统参与了 ACD 的强化特性,并表明 ERK 的参与。NTX 和 NLZ 降低 ACD 但不降低蔗糖自我给药的发现表明,这些作用是 ACD 特异性的。