Faculty of Pharmacy, Universitas Hasanuddin, Makassar, South Sulawesi, Indonesia.
Faculty of Medicine, Universitas Hasanuddin, Makassar, South Sulawesi, Indonesia.
Arch Razi Inst. 2021 Dec 30;76(6):1645-1654. doi: 10.22092/ARI.2021.356628.1884. eCollection 2021 Dec.
A comprehensive investigation into drug candidates with nootropic activity using a proper and high throughput yet economical model organism is an important issue to consider. This proof-of-concept study was carried out to determine whether can be used as an screening platform to assess the nootropic activity of certain candidates for the treatment of neurodegenerative diseases. To test this, caffeine was used as a nootropic compound and a Drosophila mutant line lacking PGRP-LB with hyperactivation of NF-κB leading to early death with neurodegenerative phenotype was used as a model organism. Caffeine was orally administered via food to the PGRP-LB mutant of at different concentrations (0.4 mM, 0.08 mM, 0.016 mM) prior to phenotypical observations of the survival and locomotor activity, as well as gene expression analysis, to assess the expression level of , , and genes. The results pointed out that the lifespan of treated with 0.016 mM caffeine was dramatically increased; nonetheless, no changes were observed in the locomotor activity. Phenotypical analysis using a T-maze vial test demonstrated a good cognitive improvement in response to caffeine administration. Molecular analysis revealed that caffeine at a concentration of 0,016 mM induced the expression of the endogenous antioxidant genes and , but not , signifying that the increased lifespan may be associated with a marked improvement in cytoplasmic antioxidant function. In general, the findings of the present study are in line with those previously observed in the mammalian model organism. Therefore, it can be concluded that can be used as a model organism in preliminary investigation and screening of nootropic candidates prior to further testing in its mammalian counterparts.
使用适当且高通量但经济的模式生物全面研究具有益智活性的药物候选物是一个需要考虑的重要问题。本概念验证研究旨在确定 是否可以用作 筛选平台,以评估某些治疗神经退行性疾病候选药物的益智活性。为此,使用咖啡因作为益智化合物,并且使用缺乏 PGRP-LB 的果蝇突变体系作为模型生物,该突变体系中 NF-κB 的过度激活导致具有神经退行性表型的早期死亡。通过食物将咖啡因以不同浓度(0.4 mM、0.08 mM、0.016 mM)口服给予 的 PGRP-LB 突变体,然后观察生存和运动活性的表型以及基因表达分析,以评估 、 和 基因的表达水平。结果表明,用 0.016 mM 咖啡因处理的 的寿命显著延长;然而,运动活性没有变化。使用 T 型迷津瓶测试进行表型分析表明,咖啡因给药后认知能力有了很好的改善。分子分析表明,浓度为 0.016 mM 的咖啡因诱导内源性抗氧化基因 和 的表达,但不诱导 的表达,表明寿命的延长可能与细胞质抗氧化功能的显著改善有关。总的来说,本研究的结果与以前在哺乳动物模型生物中观察到的结果一致。因此,可以得出结论, 可以用作在进一步在其哺乳动物对应物中进行测试之前对益智候选物进行初步研究和筛选的模型生物。