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α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)型谷氨酸受体正变构调节剂对小鼠苯二氮䓬类诱导的空间辨别缺陷的影响。

Effects of positive modulators of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-type glutamate receptors in a benzodiazepine-induced deficit of spatial discrimination in mice.

机构信息

Institut de Recherches Servier, Croissy-sur-Seine, France.

出版信息

J Psychopharmacol. 2012 Jun;26(6):845-56. doi: 10.1177/0269881111416692. Epub 2011 Sep 2.

Abstract

Imbalance between GABAergic and glutamatergic neurotransmission has been recently hypothesized to trigger memory decline related either to ageing or to Alzheimer's disease (AD). Thereby, benzodiazepine-induced anterograde amnesia has been construed as a model of hippocampal-related cognitive dysfunctions. Since spatial memory is altered both by ageing and by benzodiazepines such as alprazolam, we investigated the pharmacological sensitivity of alprazolam-induced deficit in a delayed spatial discrimination (SD) task, notably with positive allosteric modulators of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-type glutamate receptors. We showed that alprazolam (0.1 mg/kg intraperitoneally) induced memory impairments as compared with vehicle-treated mice. The oral administration of modulators of AMPA receptors (IDRA-21: 10 mg/kg; S18986: 3 and 10 mg/kg) reversed the alprazolam-induced deficits. This study is first to show evidence that reference treatments of AD, such as memantine (a NMDA receptor antagonist) at 3 mg/kg per os (po) and donepezil (an acetylcholinesterase inhibitor) at 1 mg/kg po, also reversed the alprazolam-induced amnesia. Given such results, the SD task emerges as a valuable novel task to screen pro-cognitive compounds. Thus, we highlight the efficacy of modulators of AMPA-type glutamate receptors to counteract alprazolam-induced spatial deficits. These results could be viewed alongside the imbalance between excitation and inhibition observed during normal and pathological ageing.

摘要

GABA 能和谷氨酸能神经递质之间的失衡最近被假设为触发与衰老或阿尔茨海默病 (AD) 相关的记忆减退。因此,苯二氮䓬类药物引起的顺行性遗忘被构造成与海马相关的认知功能障碍的模型。由于空间记忆既会因衰老而改变,也会因苯二氮䓬类药物(如阿普唑仑)而改变,我们研究了阿普唑仑在延迟空间辨别 (SD) 任务中引起的缺陷的药物敏感性,特别是使用 α-氨基-3-羟基-5-甲基-4-异恶唑丙酸 (AMPA) 型谷氨酸受体的正变构调节剂。我们发现,与接受载体处理的小鼠相比,阿普唑仑 (0.1mg/kg 腹腔内注射) 引起记忆损伤。AMPA 受体调节剂 (IDRA-21:10mg/kg;S18986:3 和 10mg/kg) 的口服给药逆转了阿普唑仑引起的缺陷。这项研究首次证明了 AD 的参考治疗方法,如口服 3mg/kg 美金刚 (NMDA 受体拮抗剂) 和口服 1mg/kg 多奈哌齐 (乙酰胆碱酯酶抑制剂),也可以逆转阿普唑仑引起的遗忘。鉴于这些结果,SD 任务作为筛选促认知化合物的有价值的新任务出现。因此,我们强调了 AMPA 型谷氨酸受体调节剂对抗阿普唑仑引起的空间缺陷的功效。这些结果可以与正常和病理性衰老期间观察到的兴奋和抑制之间的失衡相提并论。

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