Screening and identification of neuroprotective compounds relevant to Alzheimer's disease from medicinal plants of S. Tome e Principe

被引:34
作者
Currais, Antonio [1 ]
Chiruta, Chandramouli [1 ]
Goujon-Svrzic, Marie [1 ]
Costa, Gustavo [2 ,3 ]
Santos, Tania [2 ,3 ]
Batista, Maria Teresa [2 ,3 ]
Paiva, Jorge [4 ]
Madureira, Maria do Ceu [4 ]
Maher, Pamela [1 ]
机构
[1] Salk Inst Biol Studies, La Jolla, CA 92037 USA
[2] Univ Coimbra, Fac Pharm, Ctr Pharmaceut Studies, P-3000548 Coimbra, Portugal
[3] Univ Coimbra, Ctr Neurosci & Cell Biol, P-3004517 Coimbra, Portugal
[4] Univ Coimbra, Dept Life Sci, Ctr Funct Ecol, P-3004516 Coimbra, Portugal
关键词
Aging; Alzheimer; Dementia; Inflammation; Neurodegenerative disorders; Traditional medicine Africa; INDOLE ALKALOIDS; FISETIN; ACTIVATION; MECHANISMS; BRAIN; CELLS; MICE; DIFFERENTIATION; MODULATION; FLAVONOIDS;
D O I
10.1016/j.jep.2014.06.046
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Ethnopharmacological relevance: Alzheimer's disease (AD) neuropathology is strongly associated with the activation of inflammatory pathways, and long-term use of anti-inflammatory drugs reduces the risk of developing the disease. In S. Tome e Principe (SW), several medicinal plants are used both for their positive effects in the nervous system (treatment of mental disorders, analgesics) and their anti-inflammatory properties. The goal of this study was to determine whether a phenotypic, cell-based screening approach can be applied to selected plants from STP (Voacanga africana, Tarenna nitiduloides, Sacosperma paniculatum, Psychotria principensis, Psychotria subobliqua) in order to identify natural compounds with multiple biological activities of interest for AD therapeutics. Materials and methods: Plant hydroethanolic extracts were prepared and tested in a panel of phenotypic screening assays that reflect multiple neurotoxicity pathways relevant to AD-oxytosis in hippocampal nerve cells, in vitro ischemia, intracellular amyloid toxicity, inhibition of microglial inflammation and nerve cell differentiation. HPLC fractions from the extract that performed the best in all of the assays were tested in the oxytosis assay, our primary Screen, and the most protective fraction was analyzed by mass spectrometry. The predominant compound was purified, its identity confirmed by ESI mass spectrometry and NMR, and then tested in all of the screening assays to determine its efficacy. Results: An extract from the bark of Voacanga africana was more protective than any other plant extract in all of the assays (EC(50)s <= 2.4 mu g/mL). The HPLC fraction from the extract that was most protective against oxytosis contained the alkaloid voacamine (MW = 704.90) as the predominant compound. Purified voacamine was very protective at low doses in all of the assays (EC(50)s <= 3.4 mu M). Conclusion: These findings validate the use of our phenotypic screening, cell-based assays to identify potential compounds to treat AD from plant extracts with ethnopharmacological relevance. Our study identifies the alkaloid voacamine as a major compound in Voacanga africana with potent neuroprotective activities in these assays. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:830 / 840
页数:11
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