Behavioral Neuroscience Branch, National Institute on Drug Abuse–Intramural Research Program, National Institutes of Health, DHHS,333 Cassell Drive, Baltimore, MD 21224, USA.
Brain Res. 2011 Apr 6;1383:141-53. doi: 10.1016/j.brainres.2011.01.092. Epub 2011 Feb 2.
Nicotine (NIC) is a highly addictive substance that interacts with different subtypes of nicotinic acetylcholine receptors widely distributed in the central and peripheral nervous systems. While the direct action of NIC on central neurons appears to be essential for its reinforcing properties, the role of peripheral actions of this drug remains a matter of controversy. In this study, we examined changes in locomotor activity and temperature fluctuations in the brain (nucleus accumbens and ventral tegmental area), temporal muscle, and skin induced by intravenous (iv) NIC at low human-relevant doses (10 and 30μg/kg) in freely moving rats. These effects were compared to those induced by social interaction, an arousing procedure that induces behavioral activation and temperature responses via pure neural mechanisms, and iv injections of a peripherally acting NIC analog, NIC pyrrolidine methiodide (NIC-PM) used at equimolar doses. We found that NIC at 30μg/kg induces a modest locomotor activation, rapid and strong decrease in skin temperature, and weak increases in brain and muscle temperature. While these effects were qualitatively similar to those induced by social interaction, they were much weaker and showed a tendency to increase with repeated drug administrations. In contrast, NIC-PM did not affect locomotion and induced much weaker than NIC increases in brain and muscle temperatures and decreases in skin temperature; these effects showed a tendency to be weaker with repeated drug administrations. Our data indicate that NIC's actions in the brain are essential to induce locomotor activation and brain and body hyperthermic responses. However, rapid peripheral action of NIC on sensory afferents could be an important factor in triggering its central effects, contributing to neural and physiological activation following repeated drug use.
尼古丁(NIC)是一种高度成瘾的物质,它与中枢和外周神经系统中广泛分布的不同亚型烟碱型乙酰胆碱受体相互作用。虽然 NIC 对中枢神经元的直接作用似乎是其强化特性的关键,但该药物的外周作用的作用仍然存在争议。在这项研究中,我们在自由活动的大鼠中检查了静脉内(iv)NIC 在低人类相关剂量(10 和 30μg/kg)下引起的运动活动和大脑(伏隔核和腹侧被盖区)、颞肌和皮肤的温度波动变化。这些效应与社交互动引起的效应进行了比较,社交互动是一种通过纯神经机制引起行为激活和温度反应的唤醒程序,并且静脉内注射了等效剂量的外周作用 NIC 类似物,NIC 吡咯烷甲碘化物(NIC-PM)。我们发现,30μg/kg 的 NIC 引起适度的运动激活、皮肤温度的快速和强烈下降以及大脑和肌肉温度的微弱升高。虽然这些效应与社交互动引起的效应在性质上相似,但它们要弱得多,并且随着重复给药而有增加的趋势。相比之下,NIC-PM 不影响运动,并且引起的大脑和肌肉温度升高以及皮肤温度降低的作用比 NIC 弱得多;这些效应随着重复给药而有减弱的趋势。我们的数据表明,NIC 在大脑中的作用对于诱导运动激活和大脑和身体的发热反应是必不可少的。然而,NIC 对感觉传入的快速外周作用可能是触发其中枢作用的一个重要因素,有助于重复使用药物后神经和生理的激活。