Okas Michael, Kastner Abigail, Gioia Dominic, Woodward John J
Department of Neuroscience, Medical University of South Carolina, Charleston, SC, United States.
Front Neurosci. 2023 Aug 3;17:1235866. doi: 10.3389/fnins.2023.1235866. eCollection 2023.
Although volatile organic solvents such as toluene are used for commercial and industrial uses, they are often voluntarily inhaled for their intoxicating and euphoric effects. Research into the effects of inhalants such as toluene on brain function have revealed actions on a variety of ligand-gated and voltage-activated ion channels involved in regulating neuronal excitability. Previous work from this laboratory has also shown that brief exposures to toluene vapor induce changes in the intrinsic excitability and synaptic transmission of neurons within the medial prefrontal cortex and ventral tegmental area that vary depending on projection target. In the present study, we recorded current-evoked spiking of medium spiny neurons (MSNs) in the nucleus accumbens (NAc) core and shell in adolescent rats exposed to an intoxicating concentration of toluene vapor. Compared to air controls, firing of NAc core MSNs in Sprague-Dawley rats was not altered 24 h after exposure to 10,500 ppm toluene vapor while spiking of NAc shell MSNs was enhanced at low current steps but reduced at higher current steps. When the rheobase current was used to putatively identify MSN subtypes, both "D1-like" and "D2-like" MSNs within the NAc shell but not core showed toluene-induced changes in firing. As toluene may itself have altered the rheobase resulting in misclassification of neuron subtype, we conducted additional studies using adolescent D2-Cre rats infused with a Cre-dependent mCherry reporter virus. Following toluene vapor exposure, spiking of NAc shell D2+ MSNs was enhanced at low current steps but inhibited at higher currents as compared to air controls while there were no differences in the firing of NAc shell D2- MSNs. The toluene-induced change in NAc D2+ shell MSN firing was accompanied by alterations in membrane resistance, rheobase, action potential rise time and height with no changes noted in D2- MSNs. Overall, these data add to a growing literature showing that brief exposures to intoxicating concentrations of toluene vapor causes selective alterations in the excitability of neurons within the addiction neurocircuitry that vary depending on sub-region, cell-type and projection target.
尽管甲苯等挥发性有机溶剂用于商业和工业用途,但人们常因它们的致醉和欣快作用而主动吸入。对甲苯等吸入剂对脑功能影响的研究揭示了其对多种参与调节神经元兴奋性的配体门控和电压激活离子通道的作用。本实验室之前的研究还表明,短暂暴露于甲苯蒸气会引起内侧前额叶皮质和腹侧被盖区神经元的内在兴奋性和突触传递发生变化,这些变化因投射靶点而异。在本研究中,我们记录了暴露于致醉浓度甲苯蒸气的青春期大鼠伏隔核(NAc)核心区和壳区中棘神经元(MSNs)的电流诱发放电。与空气对照组相比,暴露于10,500 ppm甲苯蒸气24小时后,斯普拉格-道利大鼠NAc核心区MSNs的放电没有改变,而NAc壳区MSNs在低电流步长时放电增强,但在高电流步长时放电减少。当用阈电流来推定识别MSN亚型时,NAc壳区而非核心区的“D1样”和“D2样”MSNs均表现出甲苯诱导的放电变化。由于甲苯本身可能改变了阈电流,导致神经元亚型分类错误,我们使用注入了Cre依赖性mCherry报告病毒的青春期D2-Cre大鼠进行了额外研究。与空气对照组相比,暴露于甲苯蒸气后,NAc壳区D2+ MSNs在低电流步长时放电增强,但在高电流时受到抑制,而NAc壳区D2- MSNs的放电没有差异。甲苯诱导的NAc D2+壳区MSN放电变化伴随着膜电阻、阈电流、动作电位上升时间和幅度的改变,而D2- MSNs没有变化。总体而言,这些数据进一步证明,短暂暴露于致醉浓度的甲苯蒸气会导致成瘾神经回路中神经元的兴奋性发生选择性改变,这些改变因亚区域、细胞类型和投射靶点而异。