小檗碱
乙酰胆碱酯酶
化学
药理学
塔克林
体内
生物利用度
巴马汀
细胞毒性
胆碱酯酶
生物碱
生物化学
阿切
体外
酶
立体化学
生物
生物技术
作者
Fernanda Vitória Leimann,Luma Borges de Souza,Byanca Pereira Moreira de Oliveira,Bruna Franzon Rossi,Patrícia Sabino da Silva,Carlos S. H. Shiraishi,Vanessa Kaplum,Rui M.V. Abreu,Carla Pereira,Lillian Barros,Ana Paula Peron,Rafael Porto Ineu,Bruno Francisco Oechsler,Cláudia Sayer,Pedro Henrique Hermes de Araújo,Odinei Hess Gonçalves
标识
DOI:10.1016/j.foodres.2023.113295
摘要
Researchers have concentrated efforts in the search for natural-based reversible inhibitors for cholinesterase enzymes as they may play a key role in the treatment of degenerative diseases. Diverse plant alkaloids can inhibit the action of acetylcholinesterase and, among them, berberine is a promising bioactive. However, berberine has poor water solubility and low bioavailability, which makes it difficult to use in treatment. The solid dispersion technique can improve the water affinity of hydrophobic substances, but berberine solid dispersions have not been extensively studied. Safety testing is also essential to ensure that the berberine-loaded solid dispersions are safe for use. This study investigated the effectiveness of berberine-loaded solid dispersions (SD) as inhibitors of acetylcholinesterase enzyme (AChE). Docking simulation was used to investigate the influence of berberine on AChE, and in vitro assays were conducted to confirm the enzymatic kinetics of AChE in the presence of berberine. Berberine SD also showed improved cytotoxic effects on tumoral cells when dispersed in aqueous media. In vivo assays using Allium cepa were implemented, and no cytotoxicity/genotoxicity was found for the berberine solid dispersion. These results suggest that berberine SD could be a significant step towards safe nanostructures for use in the treatment of neurodegenerative diseases.
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