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YZG - 331镇静催眠作用的机制研究

The mechanism study of YZG-331 on sedative and hypnotic effects.

作者信息

Tang Bo, Yu Yuanzhi, Yu Fengting, Fang Jinyu, Wang Guibin, Jiang Jianwei, Han Qinghua, Shi Jiangong, Zhang Jianjun

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.

出版信息

Behav Brain Res. 2022 Jun 25;428:113885. doi: 10.1016/j.bbr.2022.113885. Epub 2022 Apr 6.

Abstract

YZG-331 is a synthetic novel derivates of N-(4-hydroxybenzyl) adenine riboside (NHBA), which has potent sedative and hypnotic effects based on our previous study. We are now aiming to investigate the mechanism of YZG-331. In this research, the behavioral studies showed that YZG-331 (4, 8, 16 mg/kg, i.g.) could reduce the spontaneous locomotor activity in mice, which could be blocked by AM (non-selective adenosine receptor antagonist), DPCPX (adenosine A receptor (AR) antagonist), and SCH58261 (adenosine A receptor (AR) antagonist). Moreover, YZG-331 no longer exerted sedative effect in AR or AR knockdown mice. YZG-331 (2.5, 5, 10 mg/kg, i.g.) prolonged sleeping time in pentobarbital sodium treated mice, which can be prevented by DPCPX or SCH58261. The above results demonstrated that YZG-331 exerted sedative and hypnotic effects through AR and AR. In addition, it was found that YZG-331 (25, 50, 100 μM) decreased intracellular calcium level and YZG-331 (10 mg/kg, i.g.) decreased CaMKII phosphorylation (pCaMKII) level in mouse hypothalamus and cortex. In summary, this study indicated that activation of AR/ AR and down regulation of Ca-CaMKII signaling pathway were involved in the sedative and hypnotic effects of YZG-331.

摘要

YZG-331是N-(4-羟基苄基)腺嘌呤核苷(NHBA)的一种新型合成衍生物,根据我们之前的研究,它具有强大的镇静和催眠作用。我们现在旨在研究YZG-331的作用机制。在这项研究中,行为学研究表明,YZG-331(4、8、16mg/kg,腹腔注射)可降低小鼠的自发运动活性,这可被AM(非选择性腺苷受体拮抗剂)、DPCPX(腺苷A受体(AR)拮抗剂)和SCH58261(腺苷A受体(AR)拮抗剂)阻断。此外,YZG-331在AR或AR基因敲低的小鼠中不再发挥镇静作用。YZG-331(2.5、5、10mg/kg,腹腔注射)可延长戊巴比妥钠处理小鼠的睡眠时间,这可被DPCPX或SCH58261阻止。上述结果表明,YZG-331通过AR和AR发挥镇静和催眠作用。此外,发现YZG-331(25、50、100μM)可降低细胞内钙水平,YZG-331(10mg/kg,腹腔注射)可降低小鼠下丘脑和皮层中CaMKII的磷酸化(pCaMKII)水平。总之,本研究表明AR/AR的激活和Ca-CaMKII信号通路的下调参与了YZG-331的镇静和催眠作用。

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