Flavonoids in Neurodegeneration: Limitations and Strategies to Cross CNS Barriers

被引:30
作者
Andrade, Paula Branquinho [1 ]
Grosso, Clara [1 ]
Valentao, Patricia [1 ]
Bernardo, Joao [1 ]
机构
[1] Univ Porto, Fac Farm, Rua Jorge de Viterbo Ferreira 228, P-4050313 Oporto, Portugal
关键词
Flavonoids; brain-delivery; blood-brain-barrier; permeability; transporters; nano-carriers; neurodegeneration; BLOOD-BRAIN-BARRIER; CENTRAL-NERVOUS-SYSTEM; SOLID LIPID NANOPARTICLES; LONG-TERM POTENTIATION; EPITHELIAL-CELL LINES; IN-VITRO; P-GLYCOPROTEIN; TISSUE DISTRIBUTION; DRUG-DELIVERY; NATURAL-PRODUCTS;
D O I
10.2174/0929867323666160809094934
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The central nervous system (CNS) is a mythical target for drug delivery. There is an ongoing debate over the brain accessibility of flavonoids, a group of plant-derived secondary metabolites widely known by their multifarious bioactivities achieved by distinct mechanisms. Recently, their applicability in the management of neurologic and psychiatric disorders, such as Alzheimer's and Parkinson's diseases, and major depression, has received particular attention. To reach their target, flavonoids must cross over the ultimate obstacle the blood-brain barrier - at pharmacologically effective concentrations. This review addresses the low brain-bioavailability issue, based on in vitro and in vivo evidences. Besides the lipophilic character of the flavonoids, their permeability will depend upon the role of membrane transporters, especially those from the ABC superfamily. The enzymatic elements, namely beta-glucuro-nidase, can induce a transient deconjugation process and affect permeability, as well. Novel drug delivery systems are successful strategies to overcome the low bioavailability issue, and redirect the native forms to CNS-targets. This work bridges a solid opinion over this hot topic of medicinal chemistry and natural products research.
引用
收藏
页码:4151 / 4174
页数:24
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