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α-2肾上腺素能受体对快速眼动睡眠剥夺所致记忆保持缺陷的影响。

The effect of alpha-2 adrenergic receptors on memory retention deficit induced by rapid eye movement sleep deprivation.

作者信息

Norozpour Yaser, Nasehi Mohammad, Sabouri-Khanghah Vahid, Nami Mohammad, Vaseghi Salar, Zarrindast Mohammad-Reza

机构信息

Department of Cognitive Neuroscience, Institute for Cognitive Science Studies (ICSS), Tehran, Iran.

Cognitive and Neuroscience Research Center (CNRC), Amir-Almomenin Hospital, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.

出版信息

Iran J Basic Med Sci. 2020 Dec;23(12):1571-1575. doi: 10.22038/ijbms.2020.44891.10468.

Abstract

OBJECTIVES

Evidence shows that sleep deprivation (SD) disrupts the formation of hippocampus-related memories. Moreover, α2 adrenergic receptors that are wildly expressed in the CA1 hippocampal region have a significant role in modulating both sleep and memory formation. In the present research, we wanted to investigate the effect of stimulation and blockage of CA1 α2 adrenergic receptors by clonidine (an agonist of α2 adrenergic receptor) and yohimbine (an antagonist of α2 adrenergic receptor), respectively, on memory retention impairment induced by REM SD (RSD) in rats.

MATERIALS AND METHODS

Multiple platform apparatus were used to induce RSD, and the passive avoidance task was used to assess memory consolidation. Clonidine and yohimbine were injected intra-CA1.

RESULTS

The results showed that RSD (for 24 and 36, but not 12 hr) decreased memory retention, with no effect on locomotion. Post-training intra-CA1 infusion of a subthreshold dose of yohimbine (0.001 μg/rat) did not alter, while clonidine (0.1 μg/rat) restored memory retention impairment induced by RSD (24 and 36 hr). Also, none of the interventions did not influence locomotor activity.

CONCLUSION

Our data strongly showed that CA1 α2 adrenergic receptors have a critical role in RSD-induced memory retention impairment.

摘要

目的

有证据表明,睡眠剥夺(SD)会干扰与海马体相关的记忆形成。此外,在海马体CA1区广泛表达的α2肾上腺素能受体在调节睡眠和记忆形成方面具有重要作用。在本研究中,我们分别用可乐定(一种α2肾上腺素能受体激动剂)和育亨宾(一种α2肾上腺素能受体拮抗剂)刺激和阻断CA1区的α2肾上腺素能受体,以研究其对快速眼动睡眠剥夺(RSD)诱导的大鼠记忆保持受损的影响。

材料与方法

使用多平台装置诱导RSD,并采用被动回避任务评估记忆巩固。可乐定和育亨宾经CA1区注射。

结果

结果显示,RSD(24小时和36小时,但不是12小时)会降低记忆保持能力,对运动能力没有影响。训练后在CA1区注射阈下剂量的育亨宾(0.001μg/只大鼠)没有改变记忆保持能力,而可乐定(0.1μg/只大鼠)则恢复了由RSD(24小时和36小时)诱导的记忆保持损伤。此外,所有干预措施均未影响运动活动。

结论

我们的数据有力地表明,CA1区的α2肾上腺素能受体在RSD诱导的记忆保持损伤中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40f5/7811809/2c56936a9dc7/IJBMS-23-1571-g001.jpg

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