Havermans Anne, Zwart Edwin P, Cremers Hans W J M, van Schijndel Maarten D M, Constant Romy S, Mešković Maja, Worutowicz Laura X, Pennings Jeroen L A, Talhout Reinskje, van der Ven Leo T M, Heusinkveld Harm J
Centre for Health Protection, National Institute for Public Health and the Environment (RIVM), P.O. Box 1, 3720 BA Bilthoven, The Netherlands.
Toxics. 2021 Oct 7;9(10):250. doi: 10.3390/toxics9100250.
Tobacco use is the leading cause of preventable death worldwide and is highly addictive. Nicotine is the main addictive compound in tobacco, but less is known about other components and additives that may contribute to tobacco addiction. The zebrafish embryo (ZFE) has been shown to be a good model to study the toxic effects of chemicals on the neurological system and thus may be a promising model to study behavioral markers of nicotine effects, which may be predictive for addictiveness. We aimed to develop a testing protocol to study nicotine tolerance in ZFE using a locomotion test with light-dark transitions as behavioral trigger. Behavioral experiments were conducted using three exposure paradigms: (1) Acute exposure to determine nicotine's effect and potency. (2) Pre-treatment with nicotine dose range followed by a single dose of nicotine, to determine which pre-treatment dose is sufficient to affect the potency of acute nicotine. (3) Pre-treatment with a single dose combined with acute exposure to a dose range to confirm the hypothesized decreased potency of the acute nicotine exposure. These exposure paradigms showed that (1) acute nicotine exposure decreased ZFE activity in response to dark conditions in a dose-dependent fashion; (2) pre-treatment with increasing concentrations dose-dependently reversed the effect of acute nicotine exposure; and (3) a fixed pre-treatment dose of nicotine induced a decreased potency of the acute nicotine exposure. This effect supported the induction of tolerance to nicotine by the pre-treatment, likely through neuroadaptation. The interpretation of these effects, particularly in view of prediction of dependence and addictiveness, and suitability of the ZFE model to test for such effects of other compounds than nicotine, are discussed.
吸烟是全球可预防死亡的首要原因,且极易使人上瘾。尼古丁是烟草中的主要成瘾成分,但对于可能导致烟草成瘾的其他成分和添加剂,人们了解较少。斑马鱼胚胎(ZFE)已被证明是研究化学物质对神经系统毒性作用的良好模型,因此可能是研究尼古丁作用行为标志物的有前景的模型,这些标志物可能对成瘾性具有预测性。我们旨在开发一种测试方案,使用明暗转换的运动测试作为行为触发因素来研究ZFE对尼古丁的耐受性。行为实验采用三种暴露模式进行:(1)急性暴露以确定尼古丁的作用和效力。(2)用尼古丁剂量范围进行预处理,然后给予单剂量尼古丁,以确定哪种预处理剂量足以影响急性尼古丁的效力。(3)用单剂量进行预处理并结合急性暴露于剂量范围,以确认急性尼古丁暴露效力降低的假设。这些暴露模式表明:(1)急性尼古丁暴露以剂量依赖的方式降低了ZFE在黑暗条件下的活动;(2)用递增浓度进行预处理以剂量依赖的方式逆转了急性尼古丁暴露的作用;(3)固定的尼古丁预处理剂量导致急性尼古丁暴露的效力降低。这种效应支持了预处理诱导对尼古丁的耐受性,可能是通过神经适应实现的。本文讨论了这些效应(特别是考虑到对依赖性和成瘾性的预测)的解释,以及ZFE模型用于测试除尼古丁外其他化合物此类效应的适用性。