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AZD3480,一种烟碱型乙酰胆碱受体激动剂,和多奈哌齐对 D-型丝氨酸诱导的大鼠注意力损伤的影响。

Effects of AZD3480, a neuronal nicotinic acetylcholine receptor agonist, and donepezil on dizocilpine-induced attentional impairment in rats.

机构信息

Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Box 104790, Durham, NC 27710, USA.

出版信息

Psychopharmacology (Berl). 2012 Oct;223(3):251-8. doi: 10.1007/s00213-012-2712-2. Epub 2012 Apr 20.

Abstract

BACKGROUND AND RATIONALE

Nicotinic acetylcholine systems play major roles in cognitive function. Nicotine and a variety of nicotinic agonists improve attention, and nicotinic antagonist exposure impairs it. This study was conducted to investigate the effect of a novel nicotinic receptor agonist at α4β2 nicotinic receptors (AZD3480) on attention and reversal of pharmacologically induced attentional impairment produced by the NMDA glutamate antagonist dizocilpine (MK-801).

METHODS

Adult female Sprague-Dawley rats were trained to perform an operant visual signal detection task to a stable baseline of accuracy. The rats were then injected subcutaneously following a repeated measures, counter-balanced design with saline, AZD3480 (0.01, 0.1, and 1 mg/kg), dizocilpine (0.05 mg/kg), or their combinations 30 min before the test. The effect of donepezil on the same pharmacologically induced attentional impairment was also tested. A separate group of rats was injected with donepezil (0.01, 0.1, and 1 mg/kg), dizocilpine (0.05 mg/kg), or their combinations, and their attention were assessed. Saline was the vehicle control.

RESULTS

Dizocilpine caused a significant (p < 0.0005) impairment in percent correct performance. This attentional impairment was significantly (p < 0.0005) reversed by 0.01 and 0.1 mg/kg of AZD3480. AZD3480 by itself did not alter the already high baseline control performance. Donepezil (0.01-1.0 mg/kg) also significantly (p < 0.005) attenuated the dizocilpine-induced attentional impairment.

CONCLUSIONS

AZD3480, similar to donepezil, showed significant efficacy for counteracting the attentional impairment caused by the NMDA glutamate antagonist dizocilpine. Low doses of AZD3480 may provide therapeutic benefit for reversing attentional impairment in patients suffering from cognitive impairment due to glutamatergic dysregulation and likely other attentional disorders.

摘要

背景与原理

烟碱型乙酰胆碱系统在认知功能中发挥着重要作用。尼古丁和各种烟碱激动剂可改善注意力,而烟碱拮抗剂暴露则会损害注意力。本研究旨在探究新型烟碱受体α4β2 型烟碱受体激动剂(AZD3480)对注意力的影响,以及 NMDA 谷氨酸拮抗剂地卓西平(MK-801)引起的注意力损害的逆转作用。

方法

成年雌性 Sprague-Dawley 大鼠接受操作性视觉信号检测任务训练,以达到稳定的准确率基线。然后,大鼠按照重复测量、平衡设计的方案,皮下注射盐水、AZD3480(0.01、0.1 和 1 mg/kg)、地卓西平(0.05 mg/kg)或它们的组合,在测试前 30 分钟进行注射。还测试了多奈哌齐对相同的药物引起的注意力损害的影响。一组单独的大鼠注射多奈哌齐(0.01、0.1 和 1 mg/kg)、地卓西平(0.05 mg/kg)或它们的组合,并评估它们的注意力。盐水为载体对照。

结果

地卓西平导致百分比正确表现显著(p<0.0005)受损。这种注意力损害被 0.01 和 0.1 mg/kg 的 AZD3480 显著(p<0.0005)逆转。AZD3480 本身并未改变已经很高的基线对照表现。多奈哌齐(0.01-1.0 mg/kg)也显著(p<0.005)减轻了地卓西平引起的注意力损害。

结论

AZD3480 与多奈哌齐相似,对对抗 NMDA 谷氨酸拮抗剂地卓西平引起的注意力损害具有显著疗效。AZD3480 的低剂量可能为治疗因谷氨酸能失调和可能其他注意力障碍而导致认知障碍的患者的注意力损害提供治疗益处。

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