化学
神经毒性
木犀草素
芦丁
血脑屏障
多酚
药理学
山奈酚
伞形酮
染料木素
姜黄素
非西汀
大豆黄酮
芹菜素
异黄酮
槲皮素
生物化学
抗氧化剂
类黄酮
色谱法
毒性
香豆素
中枢神经系统
内科学
医学
有机化学
神经科学
生物
作者
Rena Shimazu,Moemi Anada,Amane Miyaguchi,Yuri Nomi,Hitoshi Matsumoto
标识
DOI:10.1021/acs.jafc.1c02898
摘要
Anthocyanins (ACs) are able to protect neurons against β-amyloid-induced neurotoxicity. In this study, we evaluated blood–brain barrier (BBB) permeability of these compounds using a model kit to clarify the mechanism of AC on the brain. Black currant or strawberry AC extract was orally administrated to male Wistar rats. The urine and extirpated brain were collected before and after administration and analyzed quantitatively by liquid chromatography–tandem mass spectrometry. After administration of AC, several phenolic acids were detected in the urine samples. Further, AC and some AC metabolites were found in the brain tissue. BBB permeabilities of these compounds were much lower than the positive control. Epigallocatechin, daidzein, genistein, equol, and nobiletin presented high BBB permeability, whereas apigenin, luteolin, quercetin, and kaempferol showed medium permeability, and epicatechin, rutin, fisetin, resveratrol, and curcumin BBB permeation was neglected. These results suggested that ACs were difficult to cross BBB into the brain and ACs were not directly associated with the prevention of β-amyloid-induced neurotoxicity.
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