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首页> 外文期刊>Angewandte Chemie >Photoexcited Porphyrins as a Strong Suppressor of beta-Amyloid Aggregation and Synaptic Toxicity
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Photoexcited Porphyrins as a Strong Suppressor of beta-Amyloid Aggregation and Synaptic Toxicity

机译:光激发的卟啉作为β-淀粉样蛋白聚集和突触毒性的强抑制剂。

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摘要

The abnormal assembly of beta-amyloid (Ab) peptides into neurotoxic, beta-sheet-rich amyloid aggregates is a major pathological hallmark of Alzheimer's disease (AD). Light-induced photosensitizing molecules can regulate A beta amyloidogenesis. Multiple photochemical analyses using circular dichroism, atomic force microscopy, dot blot, and native gel electrophoresis verified that photoactivated meso-tetra(4-sulfonatophenyl)porphyrin (TPPS with M = 2H(+), Zn2+, Cu2+, Mn2+) successfully inhibits A beta aggregation in vitro. Furthermore, A beta toxicity was relieved in the photoexcited-TPP-Streated Drosophila AD model. TPPS suppresses neural cell death, synaptic toxicity, and behavioral defects in the Drosophila AD model under blue light illumination. Behavioral phenotypes, including larval locomotion defect and short lifespan caused by A beta overexpression, were also rescued by blue light-excited TPPS.
机译:β-淀粉样蛋白(Ab)肽异常组装为神经毒性,富含β-折叠的淀粉样蛋白聚集体是阿尔茨海默氏病(AD)的主要病理标志。光诱导的光敏分子可以调节Aβ淀粉样蛋白生成。使用圆二色性,原子力显微镜,斑点印迹和天然凝胶电泳进行的多次光化学分析证实,光活化的中四(4-磺酰基苯基)卟啉(TPPS的M = 2H(+),Zn2 +,Cu2 +,Mn2 +)成功抑制A beta体外聚集。此外,在光激发的TPP处理的果蝇AD模型中,β毒性得以缓解。 TPPS抑制果蝇AD模型在蓝光下的神经细胞死亡,突触毒性和行为缺陷。蓝光激发的TPPS也可以挽救行为表型,包括幼虫运动缺陷和Aβ过表达引起的寿命短。

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