Zhang Runfang, Zhao Tingkui, Zheng Beibei, Zhang Yun, Li Xiaohui, Zhang Feng, Cen Juan, Duan Shaofeng
Key Laboratory of Natural Medicine and Immune Engineering, School of Pharmacy, Henan University, Kaifeng, China.
Biology Institute, Qilu University of Technology (Shandong Academy of Sciences), Jinan, China.
Front Pharmacol. 2021 Apr 15;12:648107. doi: 10.3389/fphar.2021.648107. eCollection 2021.
In this paper, a curcumin derivative Cur20 was synthesized for better hydrolytic stability, which showed a higher angiogenic effect on zebrafish model than curcumin. In order to reveal the potential effects on neuroprotection, a mouse model of vascular dementia (VaD) induced by permanent right common carotid artery occlusion (rUCCAO) was established. After two weeks of curcumin administration, the cognitive function of mice was detected by Morris water maze and Y maze. The alteration on oxidative injuries and morphological damage were also analyzed by reactive oxygen species, superoxide dismutase, GSH, malondialdehyde tests, and Nissl stain on cortex/hippocampus. The angiogenesis and related signal factors were evaluated as well. The results showed that Cur20 significantly attenuated the cognitive dysfunction and histopathological changes of the VaD mice with enhanced antioxidant system and angiogenesis. In addition, primary rat brain microvessel endothelial cells (rBMECs) with oxygen glucose deprivation (OGD) were applied to further verify the possible mechanisms of Cur20-induced angiogenesis. The results demonstrated that the proliferation effect and the activation of pro-angiogenesis factors such as HIF-1α, VEGF, and TFEB might contribute to the protection of ischemic injury. Based on the above, our conclusion is that Cur20 can be considered as a promising therapeutic strategy for VaD.
在本文中,合成了一种姜黄素衍生物Cur20以获得更好的水解稳定性,其在斑马鱼模型上显示出比姜黄素更高的血管生成作用。为了揭示其对神经保护的潜在作用,建立了一种由永久性右颈总动脉闭塞(rUCCAO)诱导的血管性痴呆(VaD)小鼠模型。给予姜黄素两周后,通过莫里斯水迷宫和Y迷宫检测小鼠的认知功能。还通过活性氧、超氧化物歧化酶、谷胱甘肽、丙二醛检测以及对皮质/海马体进行尼氏染色来分析氧化损伤和形态损伤的变化。同时评估血管生成和相关信号因子。结果表明,Cur20显著减轻了VaD小鼠的认知功能障碍和组织病理学变化,增强了抗氧化系统和血管生成。此外,应用氧糖剥夺(OGD)的原代大鼠脑微血管内皮细胞(rBMECs)进一步验证Cur20诱导血管生成的可能机制。结果表明,增殖作用以及促血管生成因子如HIF-1α、VEGF和TFEB的激活可能有助于保护缺血性损伤。基于以上研究,我们的结论是Cur20可被视为一种有前景的VaD治疗策略。