Altabella Luisa, Sbriccoli Marco, Zoratto Francesca, Poleggi Anna, Vinci Ramona, Lacivita Enza, Leopoldo Marcello, Laviola Giovanni, Cardone Franco, Canese Rossella, Adriani Walter
Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità Rome, Italy.
Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità Rome, Italy ; Bambino Gesù Children's Hospital IRCCS Rome, Italy.
Front Behav Neurosci. 2014 Dec 16;8:427. doi: 10.3389/fnbeh.2014.00427. eCollection 2014.
LP-211 is a new, selective agonist of serotonin (5-hydroxytryptamine, 5-HT) receptor 7 (5-HT7-R), which is part of a neuro-transmission system with a proposed role in neural plasticity and in mood, cognitive and sleep regulation. Adolescent subchronic LP-211 treatment produces some persisting changes in rats' forebrain structural and functional parameters. Here, using pharmacological MRI (phMRI), we investigated the effect of acute administration with LP-211 (10 mg/kg i.p.), or vehicle, to adult rats previously exposed to the same drug (0.25 mg/kg/day for 5 days), or vehicle, during adolescence (44-48 post-natal days); histology and immuno-histochemistry were performed ex vivo to evaluate neuro-anatomical and physiological long-term adaptation to pharmacological pre-treatment. The phMRI signal reveals forebrain areas (i.e., hippocampus, orbital prefrontal cortex), activated in response to LP-211 challenge independently of adolescent pre-treatment. In septum and nucleus accumbens, sensitized activation was found in adolescent pre-treated rats but not in vehicle-exposed controls. Immuno-histochemical analyses showed marked differences in septum as long-term consequence of the adolescent pre-treatment: increased level of 5-HT7-R, increased number of 5-HT7-R positive cells, and enhanced astrocyte activation. For nucleus accumbens, immuno-histochemical analyses did not reveal any difference between adolescent pre-treated rats and vehicle-exposed controls. In conclusion, subchronic LP-211 administration during adolescence is able to induce persistent physiological changes in the septal 5-HT7-R expression and astrocyte response that can still be observed in adulthood. Data shed new insights into roles of 5-HT7-R for normal and pathologic behavioral regulations.
LP - 211是一种新型的血清素(5 - 羟色胺,5 - HT)受体7(5 - HT7 - R)选择性激动剂,5 - HT7 - R是神经传递系统的一部分,在神经可塑性以及情绪、认知和睡眠调节中发挥作用。青春期大鼠亚慢性LP - 211治疗会使大鼠前脑的结构和功能参数产生一些持续变化。在此,我们使用药物磁共振成像(phMRI)研究了对青春期(出生后44 - 48天)曾接受相同药物(0.25 mg/kg/天,共5天)或赋形剂治疗的成年大鼠急性注射LP - 211(10 mg/kg,腹腔注射)或赋形剂的效果;在体外进行组织学和免疫组织化学分析,以评估对药物预处理的神经解剖学和生理学长期适应性。phMRI信号显示,前脑区域(即海马体、眶前额叶皮质)在受到LP - 211激发时被激活,且与青春期预处理无关。在隔区和伏隔核中,青春期预处理的大鼠出现了敏化激活,而接受赋形剂处理的对照组未出现。免疫组织化学分析显示,作为青春期预处理的长期结果,隔区存在显著差异:5 - HT7 - R水平升高、5 - HT7 - R阳性细胞数量增加以及星形胶质细胞激活增强。对于伏隔核,免疫组织化学分析未显示青春期预处理的大鼠与接受赋形剂处理的对照组之间存在任何差异。总之,青春期亚慢性LP - 211给药能够诱导隔区5 - HT7 - R表达和星形胶质细胞反应的持续生理变化,在成年期仍可观察到。这些数据为5 - HT7 - R在正常和病理行为调节中的作用提供了新的见解。