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一种用于治疗老年痴呆症的新型药物候选物:来自花椒的 gx-50。

A novel drug candidate for Alzheimer's disease treatment: gx-50 derived from Zanthoxylum bungeanum.

机构信息

School of Life Science and Biotechnology, Shanghai JiaoTong University, Shanghai, China.

出版信息

J Alzheimers Dis. 2013;34(1):203-13. doi: 10.3233/JAD-121831.

Abstract

This study focused on a promising drug candidate, N-[2-(3,4-dimethoxyphenyl)ethyl]-3-phenyl-acrylamide (gx-50), a compound extracted from Sichuan pepper (Zanthoxylum Bungeanum), to determine whether it would be an effective therapeutic for Alzheimer's disease (AD) via biological experiments. In vivo, we determined the pharmacokinetic profile of gx-50 and evaluated the effect of gx-50 on the cognitive abilities of amyloid-β protein precursor transgenic (AβPP-Tg) mice by Morris water maze testing. In addition, we examined the effects of gx-50 on amyloid-β (Aβ) oligomers in the brains of AβPP-Tg mice by immunohistochemistry. In vitro, we observed a direct effect of gx-50 on Aβ oligomers by atomic force microscopy, detected the neuroprotective effects of gx-50 by western blotting and cell apoptosis assays, and measured its effects on intracellular calcium currents by laser confocal microscopy. Experiments in vivo showed that gx-50 could penetrate the blood brain barrier and improve the cognitive abilities of mice. Moreover, gx-50 treatment decreased the accumulation of Aβ oligomers in the cerebral cortex. The results in vitro demonstrated that gx-50 could disassemble Aβ oligomers, inhibit Aβ-induced neuronal apoptosis and apoptotic gene expression, and reduce neuronal calcium toxicity. These results strongly suggest that gx-50 is a potential candidate drug for treating AD.

摘要

本研究聚焦于一种有前景的药物候选物 N-[2-(3,4-二甲氧苯基)乙基]-3-苯基丙烯酰胺(gx-50),它是从四川花椒(Zanthoxylum Bungeanum)中提取的化合物,通过生物实验来确定它是否可以成为阿尔茨海默病(AD)的有效治疗药物。在体内,我们确定了 gx-50 的药代动力学特征,并通过 Morris 水迷宫测试评估了 gx-50 对淀粉样蛋白前体转基因(AβPP-Tg)小鼠认知能力的影响。此外,我们通过免疫组织化学检查了 gx-50 对 AβPP-Tg 小鼠大脑中 Aβ 寡聚物的影响。在体外,我们通过原子力显微镜观察到 gx-50 对 Aβ 寡聚物的直接作用,通过 Western blot 和细胞凋亡测定检测了 gx-50 的神经保护作用,并通过激光共聚焦显微镜测量了其对细胞内钙电流的影响。体内实验表明,gx-50 能够穿透血脑屏障并改善小鼠的认知能力。此外,gx-50 治疗可减少大脑皮层中 Aβ 寡聚物的积累。体外实验结果表明,gx-50 可以解聚 Aβ 寡聚物,抑制 Aβ 诱导的神经元凋亡和凋亡基因表达,并减少神经元钙毒性。这些结果强烈表明 gx-50 是治疗 AD 的潜在候选药物。

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