Dickson Price E, Mittleman Guy
The Jackson Laboratory, Bar Harbor, ME, United States.
Department of Psychological Science, Ball State University, Muncie, IN, United States.
Front Behav Neurosci. 2020 Jan 10;13:286. doi: 10.3389/fnbeh.2019.00286. eCollection 2019.
Sensation seeking is a heritable trait that is genetically correlated with substance use; the shared genetic mechanisms underlying these traits are largely unknown. The relationship of sensation seeking and substance use has practical importance because discovering genes that drive sensation seeking can reveal genes driving substance use, and quantification of sensation seeking in mice is higher throughput and less technically challenging than quantification of volitional drug use. In order to fully understand the genetic mechanisms driving sensation seeking, it is critical to first understand the nongenetic factors driving sensation seeking. In the present study, we used the operant sensation seeking paradigm to assess the effects of stimulus complexity on sensation seeking in C57BL/6J and DBA/2J mice. These strains are the founders of the BXD recombinant inbred mouse panel which enables the discovery of genes driving phenotypic variation. This study led to four principal conclusions. First, all sensory stimuli used in the study, regardless of complexity or number of stimulus modalities, served as reinforcers for C57BL/6J and DBA/2J mice. Second, for both C57BL/6J and DBA/2J mice, sensation seeking for a high complexity sensory stimulus was significantly greater than sensation seeking for a low complexity sensory stimulus. Third, for both C57BL/6J and DBA/2J mice, sensation seeking escalated significantly within-session when a multimodal sensory stimulus of medium or high complexity was used but not when a unimodal sensory stimulus of low complexity was used. Finally, both the magnitude of sensation seeking and the magnitude of within-session escalation of sensation seeking were significantly greater in mice from the DBA/2J strain relative to mice from the C57BL/6J strain. Collectively, these findings indicate that stimulus complexity and genetic background drive escalation of operant sensation seeking within and across sessions, and that the BXD recombinant inbred mouse panel can be used to discover the genetic mechanisms underlying these phenomena.
寻求刺激是一种可遗传的特质,与物质使用存在基因相关性;这些特质背后的共同遗传机制在很大程度上尚不清楚。寻求刺激与物质使用之间的关系具有实际重要性,因为发现驱动寻求刺激的基因可以揭示驱动物质使用的基因,并且在小鼠中对寻求刺激进行量化比量化自愿性药物使用具有更高的通量且技术挑战性更低。为了全面理解驱动寻求刺激的遗传机制,首先了解驱动寻求刺激的非遗传因素至关重要。在本研究中,我们使用操作性寻求刺激范式来评估刺激复杂性对C57BL/6J和DBA/2J小鼠寻求刺激的影响。这些品系是BXD重组近交小鼠品系的奠基者,这使得能够发现驱动表型变异的基因。本研究得出了四个主要结论。第一,研究中使用的所有感觉刺激,无论其复杂性或刺激模式数量如何,对C57BL/6J和DBA/2J小鼠来说都是强化物。第二,对于C57BL/6J和DBA/2J小鼠而言,对高复杂性感觉刺激的寻求刺激显著大于对低复杂性感觉刺激的寻求刺激。第三,对于C57BL/6J和DBA/2J小鼠,当使用中等或高复杂性的多模式感觉刺激时,寻求刺激在实验过程中显著增加,但当使用低复杂性的单模式感觉刺激时则不然。最后,相对于C57BL/6J品系的小鼠,DBA/2J品系的小鼠在寻求刺激的程度以及实验过程中寻求刺激的增加程度上都显著更大。总体而言,这些发现表明刺激复杂性和遗传背景驱动了实验过程中及不同实验之间操作性寻求刺激的增加,并且BXD重组近交小鼠品系可用于发现这些现象背后的遗传机制。