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针对尼古丁的主动免疫可阻断尼古丁的奖赏促进作用,并在一定程度上预防大鼠的尼古丁戒断,这通过伏隔核中的多巴胺输出、脑奖赏阈值和躯体体征来衡量。

Active immunisation against nicotine blocks the reward facilitating effects of nicotine and partially prevents nicotine withdrawal in the rat as measured by dopamine output in the nucleus accumbens, brain reward thresholds and somatic signs.

作者信息

Lindblom Nina, de Villiers Sabina H L, Semenova Svetlana, Kalayanov Genadiy, Gordon Sandra, Schilström Björn, Johansson Anette M, Markou Athina, Svensson Torgny H

机构信息

Department of Physiology and Pharmacology, Section of Neuropsychopharmacology, Karolinska Institutet, Nanna Svartz väg 2, 171 77, Stockholm, Sweden.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2005 Nov;372(3):182-94. doi: 10.1007/s00210-005-0019-0. Epub 2005 Nov 15.

Abstract

We recently showed that active immunisation with the nicotine immunoconjugate IP18-KLH reduces the nicotine-induced increase in dopamine (DA) output in the nucleus accumbens (NAC) and prevents reinstatement of nicotine-seeking behaviour in rats. These effects are mediated by altered distribution of nicotine, resulting in reduced amounts of nicotine reaching the brain, thereby interfering with the rewarding properties of the drug. The present study was designed to explore the effect of immunisation against nicotine on mecamylamine-precipitated nicotine withdrawal as assessed by the reduction in DA output in the NAC in rats. Measuring brain reward thresholds and somatic signs of nicotine withdrawal, the effects of immunisation were also tested during chronic nicotine treatment and after its withdrawal. Finally, we examined the effect of immunisation on challenge injections of nicotine on brain reward thresholds after the increases in somatic signs and reward thresholds associated with nicotine withdrawal had dissipated. The results show that immunisation with IP18-KLH prevented the decrease in DA output in the NAC associated with mecamylamine-precipitated nicotine withdrawal. Moreover, immunisation against nicotine did not precipitate a withdrawal syndrome, as measured by brain reward thresholds and somatic signs, in rats chronically exposed to nicotine. Furthermore, the withdrawal syndrome elicited after cessation of chronic nicotine administration was attenuated in immunised rats compared to that of mock-immunised rats. Finally, the lowering in reward thresholds after nicotine challenge injections was attenuated in both naïve and previously nicotine-exposed immunised rats. In conclusion, the present results show that immunisation with IP18-KLH did not precipitate nicotine withdrawal in rats. Thus, immunisation with IP18-KLH may not elicit nicotine withdrawal in smokers either. Furthermore, since the withdrawal syndrome in rats was attenuated by immunisation, the nicotine withdrawal in smokers should not be worsened but may even be ameliorated during a quit attempt.

摘要

我们最近发现,用尼古丁免疫偶联物IP18-KLH进行主动免疫可减少尼古丁诱导的伏隔核(NAC)中多巴胺(DA)释放增加,并防止大鼠恢复觅烟行为。这些作用是由尼古丁分布改变介导的,导致到达大脑的尼古丁量减少,从而干扰该药物的奖赏特性。本研究旨在探讨尼古丁免疫对美加明诱发的尼古丁戒断的影响,通过测量大鼠NAC中DA释放的减少来评估。通过测量脑奖赏阈值和尼古丁戒断的躯体体征,还在慢性尼古丁治疗期间及其戒断后测试了免疫的效果。最后,我们研究了在与尼古丁戒断相关的躯体体征和奖赏阈值增加消散后,免疫对尼古丁激发注射对脑奖赏阈值的影响。结果表明,用IP18-KLH免疫可防止与美加明诱发的尼古丁戒断相关的NAC中DA释放减少。此外,通过脑奖赏阈值和躯体体征测量,尼古丁免疫并未在长期暴露于尼古丁的大鼠中诱发戒断综合征。此外,与假免疫大鼠相比,免疫大鼠在慢性尼古丁给药停止后诱发的戒断综合征有所减轻。最后,在未接触过尼古丁的和先前接触过尼古丁的免疫大鼠中,尼古丁激发注射后奖赏阈值的降低均有所减轻。总之,目前的结果表明,用IP18-KLH免疫不会在大鼠中诱发尼古丁戒断。因此,用IP18-KLH免疫也可能不会在吸烟者中引发尼古丁戒断。此外,由于免疫可减轻大鼠的戒断综合征,吸烟者的尼古丁戒断在戒烟尝试期间不应恶化,甚至可能得到改善。

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