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通过腺苷 A 受体发挥的 AR-001 的催眠作用。

Hypnotic effect of AR-001 through adenosine A receptor.

机构信息

Department of Pharmacy, Ajou University, Suwon, 16499, Republic of Korea.

Department of Pharmacy, Ajou University, Suwon, 16499, Republic of Korea; AI-Super Convergence KIURI Translational Research Center, Ajou University School of Medicine, Suwon, 16499, Republic of Korea; Research Institute of Pharmaceutical Science and Technology, Ajou University, Suwon, 16499, Republic of Korea.

出版信息

Eur J Pharmacol. 2024 Oct 15;981:176847. doi: 10.1016/j.ejphar.2024.176847. Epub 2024 Jul 31.

Abstract

Insomnia is one of the most common sleep disorders, affecting 10-15% of the global population. Because classical remedies used to treat insomnia have various side effects, new therapeutics for insomnia are attracting attention. In the present study, we found that N-Ethyl-N-(furan-2-ylmethyl) quinazoline-2,4-diamine (AR-001) has adenosine A receptor agonistic activity and exhibits hypnotic efficacy by decreasing sleep onset latency and increasing total sleep time in a pentobarbital-induced sleep model. This hypnotic effect of AR-001 was significantly inhibited by the adenosine A receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX). As a result of immunohistochemistry, AR-001 was shown to increase neural activity in the sleep-promoting region, ventrolateral preoptic nucleus (VLPO), and decrease neural activity in the wake-promoting region, basal forebrain (BF), and lateral hypothalamus (LH), and that these effects of AR-001 were significantly inhibited by DPCPX treatment. In addition, AR-001 increased adenosine A receptor mRNA levels in the hypothalamus. In conclusion, this study suggests that AR-001 has a hypnotic effect, at least partially, through adenosine A receptor and may have therapeutic potential for insomnia.

摘要

失眠是最常见的睡眠障碍之一,影响全球 10-15%的人口。由于用于治疗失眠的经典疗法有各种副作用,因此新的失眠治疗方法引起了关注。在本研究中,我们发现 N-乙基-N-(呋喃-2-基甲基)喹唑啉-2,4-二胺(AR-001)具有腺苷 A 受体激动活性,并通过减少戊巴比妥诱导的睡眠模型中的睡眠潜伏期和增加总睡眠时间来表现出催眠功效。AR-001 的这种催眠作用被腺苷 A 受体拮抗剂 8-环戊基-1,3-二丙基黄嘌呤(DPCPX)显著抑制。免疫组织化学结果表明,AR-001 增加了促进睡眠的区域、腹外侧视前核(VLPO)的神经活性,并降低了促进觉醒的区域、基底前脑(BF)和外侧下丘脑(LH)的神经活性,并且 AR-001 的这些作用被 DPCPX 处理显著抑制。此外,AR-001 增加了下丘脑内的腺苷 A 受体 mRNA 水平。总之,本研究表明 AR-001 通过腺苷 A 受体具有催眠作用,至少部分如此,并且可能具有治疗失眠的潜力。

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