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丹皮酚衍生物 6'-甲基丹皮酚减轻皮质神经元和阿尔茨海默病小鼠模型中 Aβ诱导的病理生理改变。

Paeonol Derivative, 6'-Methyl Paeonol, Attenuates Aβ-Induced Pathophysiology in Cortical Neurons and in an Alzheimer's Disease Mice Model.

机构信息

Department of Family Medicine, National Taiwan University Hospital, Taipei, 100225, Taiwan.

出版信息

ACS Chem Neurosci. 2024 Feb 21;15(4):724-734. doi: 10.1021/acschemneuro.3c00633. Epub 2024 Jan 30.

Abstract

Herbs themselves and various herbal medicines are great resources for discovering therapeutic drugs for various diseases, including Alzheimer's disease (AD), one of the common neurodegenerative diseases. Utilizing mouse primary cortical neurons and DiBAC4(3), a voltage-sensitive indicator, we have set up a drug screening system and identified an herbal extraction compound, paeonol, obtained from ; this compound is able to ameliorate the abnormal depolarization induced by Aβ42 oligomers. Our aim was to further find effective paeonol derivatives since paeonol has been previously studied. 6'-Methyl paeonol, one of the six paeonol derivatives surveyed, is able to inhibit the abnormal depolarization induced by Aβ oligomers. Furthermore, 6'-methyl paeonol is able to alleviate the NMDA- and AMPA-induced depolarization. When a molecular mechanism was investigated, 6'-methyl paeonol was found to reverse the Aβ-induced increase in ERK phosphorylation. At the animal level, mice injected with 6'-methyl paeonol showed little change in their basic physical parameters compared to the control mice. 6'-Methyl paeonol was able to ameliorate the impairment of memory and learning behavior in J20 mice, an AD mouse model, as measured by the Morris water maze. Thus, paeonol derivatives could provide a structural foundation for developing and designing an effective compound with promising clinical benefits.

摘要

草药本身和各种草药都是发现治疗各种疾病(包括阿尔茨海默病(AD),一种常见的神经退行性疾病)的治疗药物的巨大资源。我们利用小鼠原代皮质神经元和 DiBAC4(3),一种电压敏感指示剂,建立了药物筛选系统,并鉴定出一种从获得的草药提取物化合物丹皮酚,该化合物能够改善 Aβ42 寡聚体诱导的异常去极化。我们的目的是进一步寻找有效的丹皮酚衍生物,因为丹皮酚以前已经进行过研究。在所研究的六种丹皮酚衍生物之一的 6'-甲基丹皮酚,能够抑制 Aβ 寡聚体诱导的异常去极化。此外,6'-甲基丹皮酚能够减轻 NMDA 和 AMPA 诱导的去极化。当研究分子机制时,发现 6'-甲基丹皮酚能够逆转 Aβ 诱导的 ERK 磷酸化增加。在动物水平上,与对照组小鼠相比,注射 6'-甲基丹皮酚的小鼠的基本生理参数几乎没有变化。6'-甲基丹皮酚能够改善 AD 小鼠模型 J20 小鼠的记忆和学习行为损伤,如 Morris 水迷宫所示。因此,丹皮酚衍生物可以为开发和设计具有潜在临床益处的有效化合物提供结构基础。

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