Ozga-Hess Jenny E, Anderson Karen G
Department of Psychology, West Virginia University, Morgantown, West Virginia, USA.
Behav Pharmacol. 2019 Oct;30(7):605-616. doi: 10.1097/FBP.0000000000000500.
Individuals with attention-deficit/hyperactivity disorder tend to make risker choices during probabilistic-discounting procedures. Thus, how common attention-deficit/hyperactivity disorder medications affect probabilistic discounting is of interest. In general, d-amphetamine increases risk-taking while atomoxetine has produced mixed effects in rats. Results from previous studies may result from genetic factors. Lewis and F344 rats have neurochemical differences that may be relevant to probabilistic discounting and how drugs affect such behavior. In this study, we evaluated dose-dependent effects of d-amphetamine and atomoxetine on probabilistic discounting of Lewis and F344. Male Lewis and F344 chose between one food pellet delivered 100% of the time and three food pellets delivered following decreasing probabilities of delivery (i.e. 100%, 66.7%, 33.3%, 16.5%, and 8.25%). Saline, d-amphetamine (0.1-1.8 mg/kg), and atomoxetine (0.1-7.8 mg/kg) were tested acutely. Lewis and F344 did not differ in choice at baseline. d-Amphetamine increased risky choice for both rat strains at low-to-moderate doses, although it did so at a lower dose (0.1 and 0.3 mg/kg) for F344 as compared to Lewis (0.3 mg/kg only). At high doses (1.0 and 1.8 mg/kg), d-amphetamine disrupted choice, increased frequencies of omitted trials, and reduced reinforcer sensitivity. Although atomoxetine increased frequencies of omitted trials at high doses (5.6 and 7.8 mg/kg), it had no effect on probabilistic discounting for either rat strain. Although Lewis and F344 differ in various types of impulsivity (i.e. motor, choice), with Lewis being the more impulsive of the two, the present results suggest that Lewis and F344 do not differ in risk-based decision-making. Effects of d-amphetamine on probabilistic discounting may be biology-dependent and differ from effects of atomoxetine.
患有注意力缺陷多动障碍的个体在概率折扣程序中往往会做出更冒险的选择。因此,常用的注意力缺陷多动障碍药物如何影响概率折扣备受关注。一般来说,右旋苯丙胺会增加冒险行为,而托莫西汀在大鼠身上产生的效果则好坏参半。先前研究的结果可能源于遗传因素。刘易斯大鼠和F344大鼠存在神经化学差异,这可能与概率折扣以及药物如何影响此类行为有关。在本研究中,我们评估了右旋苯丙胺和托莫西汀对刘易斯大鼠和F344大鼠概率折扣的剂量依赖性影响。雄性刘易斯大鼠和F344大鼠在100%时间提供的1颗食物颗粒和按递减概率提供的3颗食物颗粒(即100%、66.7%、33.3%、16.5%和8.25%)之间进行选择。对生理盐水、右旋苯丙胺(0.1 - 1.8毫克/千克)和托莫西汀(0.1 - 7.8毫克/千克)进行急性测试。刘易斯大鼠和F344大鼠在基线选择上没有差异。低至中等剂量时,右旋苯丙胺增加了两种大鼠品系的冒险选择,不过与刘易斯大鼠(仅0.3毫克/千克)相比,F344大鼠在较低剂量(0.1和0.3毫克/千克)时就出现了这种情况。高剂量(1.0和1.8毫克/千克)时,右旋苯丙胺扰乱了选择,增加了遗漏试验的频率,并降低了强化物敏感性。虽然托莫西汀在高剂量(5.6和7.8毫克/千克)时增加了遗漏试验的频率,但对两种大鼠品系的概率折扣均无影响。尽管刘易斯大鼠和F344大鼠在各种冲动性类型(即运动性、选择性)上存在差异,其中刘易斯大鼠更冲动,但目前的结果表明,刘易斯大鼠和F344大鼠在基于风险的决策方面没有差异。右旋苯丙胺对概率折扣的影响可能取决于生物学因素,且与托莫西汀的影响不同。