Grigsby Kolter, Usmani Zaynah, Anderson Justin, Ozburn Angela
Portland Veterans Affairs Medical Center, Research and Development Service, Portland, OR, United States.
Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, OR, United States.
Front Behav Neurosci. 2024 Jan 15;17:1321349. doi: 10.3389/fnbeh.2023.1321349. eCollection 2023.
Maintaining healthy and consistent levels of physical activity (PA) is a clinically proven and low-cost means of reducing the onset of several chronic diseases and may provide an excellent strategy for managing mental health and related outcomes. Wheel-running (WR) is a well-characterized rodent model of voluntary PA; however, its use in biomedical research is limited by economical and methodical constraints. Here, we showcase the DSC (Dependable, Simple, Cost-effective), open-source running wheel by characterizing 24-h running patterns in two genetically unique mouse lines: inbred High Drinking in the Dark line 1 [iHDID-1; selectively bred to drink alcohol to intoxication (and then inbred to maintain phenotype)] and Heterogeneous Stock/Northport (HS/Npt; the genetically heterogeneous founders of iHDID mice). Running distance (km/day), duration (active minutes/day) and speed (km/hour) at 13-days (acute WR; Experiment 1) and 28-days (chronic WR; Experiment 2) were comparable to other mouse strains, suggesting the DSC-wheel reliably captures murine WR behavior. Analysis of 24-h running distance supports previous findings, wherein iHDID-1 mice tend to run less than HS/Npt mice in the early hours of the dark phase and more than HS/Npt in the late hours of dark phase/early light phase. Moreover, circadian actograms were generated to highlight the broad application of our wheel design across disciplines. Overall, the present findings demonstrate the ability of the DSC-wheel to function as a high-throughput and precise tool to comprehensively measure WR behaviors in mice.
保持健康且持续的身体活动(PA)水平是一种经临床验证且低成本的降低多种慢性疾病发病几率的方法,并且可能为管理心理健康及相关结果提供极佳策略。轮转运动(WR)是一种特征明确的自愿性身体活动啮齿动物模型;然而,其在生物医学研究中的应用受到经济和方法上的限制。在此,我们通过对两个基因独特的小鼠品系的24小时跑步模式进行特征分析,展示了可靠、简单、经济高效的开源跑步轮:近交系黑暗中高饮1号线[iHDID-1;经选择性培育使其饮酒至中毒(然后近交以维持该表型)]和异质种群/北港(HS/Npt;iHDID小鼠的基因异质奠基者)。在13天(急性WR;实验1)和28天(慢性WR;实验2)时的跑步距离(千米/天)、持续时间(活跃分钟/天)和速度(千米/小时)与其他小鼠品系相当,这表明DSC轮能够可靠地捕捉小鼠的WR行为。对24小时跑步距离的分析支持了先前的研究结果,即iHDID-1小鼠在黑暗期早期的跑步量往往少于HS/Npt小鼠,而在黑暗期后期/光照期早期则多于HS/Npt小鼠。此外,还生成了昼夜活动图以突出我们的轮子设计在各学科中的广泛应用。总体而言,目前的研究结果证明了DSC轮作为一种高通量且精确的工具,能够全面测量小鼠WR行为的能力。