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δ 阿片受体激动剂 KNT-127 对小鼠脑电图活动的影响。

Effects of the delta opioid receptor agonist KNT-127 on electroencephalographic activity in mice.

机构信息

Department of Neuropsychopharmacology, National Institute of Mental Health, National Center of Neurology and Psychiatry, Tokyo, Japan.

International Institute for Integrative Sleep Medicine (WPI-IIIS), University of Tsukuba, Tsukuba, Ibaraki, Japan.

出版信息

Pharmacol Rep. 2018 Apr;70(2):350-354. doi: 10.1016/j.pharep.2017.08.018. Epub 2017 Oct 28.

DOI:10.1016/j.pharep.2017.08.018
PMID:29477045
Abstract

BACKGROUND

We previously reported that the novel selective delta opioid receptor (DOP) agonist KNT-127 did not cause convulsions in mice, whereas the prototype DOP agonist SNC80 did. Previous studies have reported that SNC80 caused electroencephalographic (EEG) disturbances in rodents. However, whether KNT-127 affects EEG responses is unknown. Therefore, the present study aimed to compare the effect of KNT-127 on EEG responses with that of SNC80 in mice.

METHODS

For behavioral experiments, male C57BL6/J mice were injected intraperitoneally with either KNT-127 (30 mg/kg) or SNC80 (30 mg/kg) and monitored for convulsions and subsequent catalepsy-like behavior for 10 min immediately after drug treatment. For EEG recording experiments, EEG electrodes were implanted into the right hemisphere. EEG signals exceeding twice the baseline amplitude were defined as seizure spikes.

RESULTS

KNT-127 did not induce convulsive or catalepsy-like behaviors in mice and did not result in seizure spikes, while significantly higher EEG power density was observed at 2 Hz. In contrast, SNC80 administration resulted in convulsive behaviors, seizure spikes, and significantly higher EEG power density between 2 and 10 Hz in mice.

CONCLUSIONS

In this study, we clearly demonstrated that KNT-127 administration induces neither convulsive effects nor seizure spikes in mice. We propose that KNT-127 should be considered a candidate compound for the development of improved DOP-based psychotropic drug that lack the convulsive properties.

摘要

背景

我们之前报道过,新型选择性δ 阿片受体(DOP)激动剂 KNT-127 不会引起小鼠惊厥,而原型 DOP 激动剂 SNC80 则会。先前的研究报告称,SNC80 会引起啮齿动物的脑电图(EEG)紊乱。然而,KNT-127 是否会影响 EEG 反应尚不清楚。因此,本研究旨在比较 KNT-127 和 SNC80 对小鼠 EEG 反应的影响。

方法

对于行为实验,雄性 C57BL6/J 小鼠经腹腔注射 KNT-127(30mg/kg)或 SNC80(30mg/kg),并在药物治疗后立即监测 10 分钟内是否出现惊厥和随后的类似僵住的行为。对于 EEG 记录实验,将 EEG 电极植入右侧大脑半球。超过基线振幅两倍的 EEG 信号被定义为癫痫发作波。

结果

KNT-127 未诱导小鼠出现惊厥或类似僵住的行为,也未导致癫痫发作波,而在 2Hz 时观察到明显更高的 EEG 功率密度。相比之下,SNC80 给药导致小鼠出现惊厥行为、癫痫发作波和 2-10Hz 之间明显更高的 EEG 功率密度。

结论

在这项研究中,我们清楚地表明,KNT-127 给药不会引起小鼠出现惊厥作用或癫痫发作波。我们提出,KNT-127 应该被视为开发缺乏惊厥特性的基于 DOP 的改良精神药物的候选化合物。

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Neuropharmacology. 2023 Jul 1;232:109526. doi: 10.1016/j.neuropharm.2023.109526. Epub 2023 Mar 31.
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Exploration of beta-arrestin isoform signaling pathways in delta opioid receptor agonist-induced convulsions.δ阿片受体激动剂诱导惊厥中β-抑制蛋白亚型信号通路的探索
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A non-convulsant delta-opioid receptor agonist, KNT-127, reduces cortical spreading depression and nitroglycerin-induced allodynia.
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