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Cutamesine可克服快速眼动睡眠剥夺诱导的记忆丧失:与σ-1受体占有率的关系。

Cutamesine Overcomes REM Sleep Deprivation-Induced Memory Loss: Relationship to Sigma-1 Receptor Occupancy.

作者信息

Ramakrishnan Nisha K, Schepers Marianne, Luurtsema Gert, Nyakas Csaba J, Elsinga Philip H, Ishiwata Kiichi, Dierckx Rudi A J O, van Waarde Aren

机构信息

Department of Nuclear Medicine and Molecular Imaging, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ, Groningen, Netherlands.

出版信息

Mol Imaging Biol. 2015 Jun;17(3):364-72. doi: 10.1007/s11307-014-0808-2.

Abstract

PURPOSE

Rapid eye movement (REM) sleep deprivation (SD) decreases cerebral sigma-1 receptor expression and causes cognitive deficits. Sigma-1 agonists are cognitive enhancers. Here, we investigate the effect of cutamesine treatment in the REM SD model.

PROCEDURES

Sigma-1 receptor occupancy (RO) in the rat brain by cutamesine was determined using 1-[2-(3,4-dimethoxyphenethyl)]-4-(3-phenylpropyl)piperazine ([(11)C]SA4503) and positron emission tomography (PET), and tissue cutamesine levels were measured by ultra performance liquid chromatography (UPLC)-MS. RO was calculated from a Cunningham-Lassen plot, based on the total distribution volume of [(11)C]SA4503 determined by Logan graphical analysis. Cognitive performance was assessed using the passive avoidance (PA) test.

RESULTS

Cutamesine at a dose of 1.0 mg/kg reversed REM SD-induced cognitive deficit and occupied 92 % of the sigma-1 receptor population. A lower dose (0.3 mg/kg) occupied 88 % of the receptors but did not significantly improve cognition.

CONCLUSION

The anti-amnesic effect of cutamesine in this animal model may be related to longer exposure at a higher dose and/or drug binding to secondary targets.

摘要

目的

快速眼动(REM)睡眠剥夺(SD)会降低大脑中σ-1受体的表达并导致认知缺陷。σ-1激动剂是认知增强剂。在此,我们研究了库他美新治疗在REM睡眠剥夺模型中的作用。

程序

使用1-[2-(3,4-二甲氧基苯乙基)]-4-(3-苯丙基)哌嗪([(11)C]SA4503)和正电子发射断层扫描(PET)测定大鼠脑中库他美新的σ-1受体占有率(RO),并通过超高效液相色谱(UPLC)-质谱法测量组织中的库他美新水平。基于通过洛根图形分析确定的[(11)C]SA4503的总分布体积,从坎宁安-拉森图计算RO。使用被动回避(PA)试验评估认知能力。

结果

1.0mg/kg剂量的库他美新可逆转REM睡眠剥夺诱导的认知缺陷,并占据92%的σ-1受体群体。较低剂量(0.3mg/kg)占据88%的受体,但未显著改善认知。

结论

在该动物模型中,库他美新的抗遗忘作用可能与较高剂量下的较长暴露时间和/或药物与次要靶点的结合有关。

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