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Pridopidine Reverses Phencyclidine-Induced Memory Impairment

机译:普利多匹定逆转苯环利定诱发的记忆障碍

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Pridopidine is in clinical trials for Huntington's disease treatment. Originally developed as a dopamine D_(2)receptor (D_(2)R) ligand, pridopidine displays about 100-fold higher affinity for the sigma-1 receptor (sigma-1R). Interestingly, pridopidine slows disease progression and improves motor function in Huntington's disease model mice and, in preliminarily reports, Huntington's disease patients. The present study examined the anti-amnesic potential of pridopidine. Thus, memory impairment was produced in mice by administration of phencyclidine (PCP, 10 mg/kg/day) for 10 days, followed by 14 days' treatment with pridopidine (6 mg/kg/day), or saline. Finally, novel object recognition performance was assessed in the animals. Mice receiving PCP and saline exhibited deficits in novel object recognition, as expected, while pridopidine treatment counteracted PCP-induced memory impairment. The effect of pridopidine was attenuated by co-administration of the sigma receptor antagonist, NE-100 (10 mg/kg). Our results suggest that pridopidine exerts anti-amnesic and potentially neuroprotective actions. These data provide new insights into the therapeutic potential of pridopidine as a pro-cognitive drug.
机译:普利多匹定正在亨廷顿氏病治疗的临床试验中。最初开发为多巴胺D_(2)受体(D_(2)R)配体的普利多匹定对sigma-1受体(sigma-1R)的亲和力高约100倍。有趣的是,普利多匹定减缓亨廷顿氏病模型小鼠以及亨廷顿氏病患者的疾病进展并改善其运动功能。本研究检查了普利多匹定的抗记忆潜力。因此,通过给予苯环利定(PCP,10mg / kg /天)10天,然后用普利多匹定(6mg / kg /天)或盐水处理14天,在小鼠中产生记忆障碍。最后,在动物中评估了新颖的物体识别性能。如预期的那样,接受PCP和盐水的小鼠在新物体识别方面表现出缺陷,而普利多匹定治疗则抵消了PCP诱导的记忆障碍。共同使用sigma受体拮抗剂NE-100(10 mg / kg)可减轻普利多匹定的作用。我们的结果表明,普利多匹定具有抗记忆删除和潜在的神经保护作用。这些数据为普利多匹定作为一种前认知药物的治疗潜力提供了新的见解。

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