Department of Nuclear Medicine, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine University, Moorenstr. 5, D-40225 Düsseldorf, Germany.
Department of Biomedical Sciences, University of Minnesota Medical School, Duluth, MN 55812, USA.
Neurobiol Learn Mem. 2023 Nov;205:107848. doi: 10.1016/j.nlm.2023.107848. Epub 2023 Oct 20.
In the present studies, we assessed the effect of the 5-HT receptor (R) agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) on motor and exploratory behaviors, object and place recognition and dopamine transporter (DAT) and serotonin transporter (SERT) binding in the rat brain. In Experiment I, motor/exploratory behaviors were assessed in an open field after injection of either 8-OH-DPAT (0.1 and 3 mg/kg) or vehicle for 30 min without previous habituation to the open field. In Experiment II, rats underwent a 5-min exploration trial in an open field with two identical objects. After injection of either 8-OH-DPAT (0.1 and 3 mg/kg) or vehicle, rats underwent a 5-min test trial with one of the objects replaced by a novel one and the other object transferred to a novel place. Subsequently, N-o-fluoropropyl-2b-carbomethoxy-3b-(4-[I]iodophenyl)-nortropane ([I]FP-CIT; 11 ± 4 MBq) was injected into the tail vein. Regional radioactivity accumulations were determined post mortem with a well counter. In both experiments, 8-OH-DPAT dose-dependently increased ambulation and exploratory head-shoulder motility, whereas rearing was dose-dependently decreased. In the test rial of Experiment II, there were no effects of 8-OH-DPAT on overall activity, sitting and grooming. 8-OH-DPAT dose-dependently impaired recognition of object and place. 8-OH-DPAT (3 mg/kg) increased DAT binding in the dorsal striatum relative to both vehicle and 0.1 mg/kg 8-OH-DPAT. Furthermore, in the ventral striatum, DAT binding was decreased after 3 mg/kg 8-OH-DPAT relative to vehicle. Findings indicate that motor/exploratory behaviors, memory for object and place and regional dopamine function may be modulated by the 5-HTR. Since, after 8-OH-DPAT, rats exhibited more horizontal and less (exploratory) vertical motor activity, while overall activity was not different between groups, it may be inferred, that the observed impairment of object recognition was not related to a decrease of motor activity as such, but to a decrease of intrinsic motivation, attention and/or awareness, which are relevant accessories of learning. Furthermore, the present findings on 8-OH-DPAT action indicate associations not only between motor/exploratory behavior and the recognition of object and place but also between the respective parameters and the levels of available DA in dorsal and ventral striatum.
在目前的研究中,我们评估了 5-羟色胺受体(R)激动剂 8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)对大鼠运动和探索行为、物体和位置识别以及多巴胺转运体(DAT)和血清素转运体(SERT)结合的影响。在实验 I 中,在没有预先适应开阔场的情况下,在注射 8-OH-DPAT(0.1 和 3mg/kg)或载体 30 分钟后,在开阔场中评估运动/探索行为。在实验 II 中,大鼠在开阔场中进行 5 分钟的探索试验,有两个相同的物体。在注射 8-OH-DPAT(0.1 和 3mg/kg)或载体后,大鼠进行了 5 分钟的测试试验,其中一个物体被一个新物体取代,另一个物体被转移到一个新的位置。随后,将 N-o-氟丙基-2b-羧基-3b-(4-[I]碘苯基)-nortropane([I]FP-CIT;11±4MBq)注入尾静脉。用井计数器在死后确定放射性核素的区域积聚。在这两个实验中,8-OH-DPAT 剂量依赖性地增加了步行和探索性的肩部运动,而后肢抬高则呈剂量依赖性减少。在实验 II 的测试试验中,8-OH-DPAT 对总体活动、坐姿和梳理行为没有影响。8-OH-DPAT 剂量依赖性地损害了对物体和位置的识别。8-OH-DPAT(3mg/kg)与载体和 0.1mg/kg 8-OH-DPAT 相比,增加了背侧纹状体中的 DAT 结合。此外,与载体相比,3mg/kg 8-OH-DPAT 后腹侧纹状体中的 DAT 结合减少。研究结果表明,5-HTR 可能调节运动/探索行为、物体和位置的记忆以及区域多巴胺功能。由于 8-OH-DPAT 后,大鼠表现出更多的水平运动和更少的(探索性)垂直运动活动,而各组之间的总体活动没有差异,因此可以推断,观察到的物体识别受损与运动活动的减少本身无关,而是与内在动机、注意力和/或意识的减少有关,这些都是学习的相关附属品。此外,目前关于 8-OH-DPAT 作用的发现不仅表明运动/探索行为与物体和位置识别之间存在关联,而且表明各自参数与背侧和腹侧纹状体中可用 DA 水平之间存在关联。