Pereira Robbert Mota, Campos Hericles Mesquita, de Oliveira Ferreira Pâmela Yasmin, Uchenna Nkaa, Silva Yohanny Souza, Okoh Victor Ifeanyi, Pruccoli Letizia, Arruda Evilanna Lima, Lião Luciano Morais, Mota Pedro Augusto Alves, Leite Jacqueline Alves, de Castro Georg Raphaela, da Matta David Henriques, Dos Santos Fernanda Cristina Alcantara, Costa Elson Alves, Tarozzi Andrea, Menegatti Ricardo, Ghedini Paulo César
Institute of Biological Sciences, Federal University of Goiás, Goiânia, GO, Brazil.
Department for Life Quality Studies, Alma Mater Studiorum - University of Bologna, Rimini, Italy.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Apr;398(4):4095-4109. doi: 10.1007/s00210-024-03526-5. Epub 2024 Oct 16.
Chrysin (CHR) is a naturally occurring flavonoid found in the human diet, recognized for its potential in preventing neurodegenerative diseases. However, its limited water solubility restricts its bioavailability and therapeutic applications. To address this issue and bolster the neuroprotective properties of CHR for potential nutraceutical or medicinal use, we investigated a novel compound, LQFM280, formed by conjugating CHR with β-d-glucose tetraacetate. We conducted both in vitro (using SH-SY5Y cells, mutant STHdhQ111/Q111 cells, and wild-type STHdhQ7/Q7 cells), and in vivo (mice) neurotoxicity experimental model induced by 3-nitropropionic acid, which mimic biological changes akin to Huntington's disease in humans. Compared to non-glycosylated CHR, LQFM280 showed superior in vitro effects in preventing neurotoxicity caused by increased mitochondrial vulnerability due to mutant huntingtin. In vivo findings demonstrated that LQFM280 has heightened efficacy in mitigating weight loss, memory and locomotor impairment, oxidative stress, and disruptions in the antioxidant defense system, as well as succinate dehydrogenase, and cholinesterase activities induced by 3-nitropropionic acid. These findings underscore the significant enhancement of chrysin's neuroprotective effects through glycosylation with β-d-glucose tetraacetate, positioning it as a promising candidate for use as a nutraceutical or food supplement to promote health benefits.
白杨素(CHR)是一种在人类饮食中天然存在的类黄酮,因其在预防神经退行性疾病方面的潜力而受到认可。然而,其有限的水溶性限制了其生物利用度和治疗应用。为了解决这个问题并增强CHR的神经保护特性以用于潜在的营养保健品或药物用途,我们研究了一种新型化合物LQFM280,它是通过将CHR与β-D-葡萄糖四乙酸酯共轭形成的。我们进行了体外实验(使用SH-SY5Y细胞、突变型STHdhQ111/Q111细胞和野生型STHdhQ7/Q7细胞)以及体内实验(小鼠),采用由3-硝基丙酸诱导的神经毒性实验模型,该模型模拟了类似于人类亨廷顿舞蹈病的生物学变化。与非糖基化的CHR相比,LQFM280在预防由突变型亨廷顿蛋白导致的线粒体易损性增加所引起的神经毒性方面表现出更优异的体外效果。体内研究结果表明,LQFM280在减轻体重减轻、记忆和运动功能障碍、氧化应激以及抗氧化防御系统、琥珀酸脱氢酶和3-硝基丙酸诱导的胆碱酯酶活性的破坏方面具有更高的功效。这些发现强调了通过与β-D-葡萄糖四乙酸酯糖基化显著增强了白杨素的神经保护作用,使其成为一种有前途的营养保健品或食品补充剂候选物,有望促进健康益处。