5-HT1A受体激动剂8-OH-DPAT调节背侧和腹侧纹状体的运动/探索活动、识别记忆和多巴胺转运体结合

IF 2.2 4区 心理学 Q3 BEHAVIORAL SCIENCES Neurobiology of Learning and Memory Pub Date : 2023-11-01 DOI:10.1016/j.nlm.2023.107848
Susanne Nikolaus , Owen Y. Chao , Markus Beu , Jan Henke , Christina Antke , An-Li Wang , Benedetta Fazari , Eduards Mamlins , Joseph P. Huston , Frederik L. Giesel
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引用次数: 0

摘要

在本研究中,我们评估了5-HT1A受体(R)激动剂8-羟基-2-(二正丙胺)四肽(8-OH-DPAT)对大鼠脑内运动和探索行为、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1中,在没有预先习惯开放区域的情况下,注射8-OH-DPAT(0.1和3 mg/kg)或车辆30分钟后,在开放区域评估运动/探索行为。在实验二中,大鼠对两个相同的物体进行了5分钟的探索试验。给大鼠注射8-OH-DPAT(0.1和3 mg/kg)或给药后,大鼠进行5分钟的试验,其中一个物体被一个新的物体取代,另一个物体转移到一个新的地方。随后,n -o-氟丙基-2b-碳甲氧基-3b-(4-[123I]碘苯基)-nortropane ([123I]FP-CIT;尾静脉注射11±4 MBq)。区域放射性累积在死后用井计数器测定。在两个实验中,8-OH-DPAT剂量依赖性地增加了行走和探索性头肩运动,而饲养则剂量依赖性地减少。在实验二的测试中,8-OH-DPAT对整体活动、坐姿和打扮没有影响。8-OH-DPAT剂量依赖性损伤物体和地点的识别。与对照剂和0.1 mg/kg 8-OH-DPAT相比,3 mg/kg 8-OH-DPAT增加了背纹状体中DAT的结合。此外,在腹侧纹状体中,与对照剂相比,3 mg/kg 8-OH-DPAT降低了DAT结合。研究结果表明,5-HT1AR可能调节运动/探索行为、对物体和地方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活动和更少的(探索性)垂直运动活动,而整体活动在各组之间没有差异,可以推断,观察到的物体识别障碍与运动活动的减少无关,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件。此外,目前关于8-OH-DPAT作用的研究结果表明,运动/探索行为与物体和地点的识别之间存在关联,而且各自的参数与背侧纹状体和腹侧纹状体的可用DA水平之间存在关联。
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The 5-HT1A receptor agonist 8-OH-DPAT modulates motor/exploratory activity, recognition memory and dopamine transporter binding in the dorsal and ventral striatum

In the present studies, we assessed the effect of the 5-HT1A 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-[123I]iodophenyl)-nortropane ([123I]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-HT1AR. 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.

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来源期刊
CiteScore
5.10
自引率
7.40%
发文量
77
审稿时长
12.6 weeks
期刊介绍: Neurobiology of Learning and Memory publishes articles examining the neurobiological mechanisms underlying learning and memory at all levels of analysis ranging from molecular biology to synaptic and neural plasticity and behavior. We are especially interested in manuscripts that examine the neural circuits and molecular mechanisms underlying learning, memory and plasticity in both experimental animals and human subjects.
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