Development of a neuroprotective potential algorithm for medicinal plants

被引:36
|
作者
Liu, Weixi [1 ]
Ma, Hang [2 ]
DaSilva, Nicholas A. [2 ]
Rose, Kenneth N. [2 ]
Johnson, Shelby L. [2 ]
Zhang, Lu [2 ]
Wan, Chunpeng [2 ]
Dain, Joel A. [1 ]
Seeram, Navindra P. [2 ,3 ]
机构
[1] Univ Rhode Isl, Dept Chem, Kingston, RI 02881 USA
[2] Univ Rhode Isl, Bioact Bot Res Lab, Coll Pharm, Dept Biomed & Pharmaceut Sci, Kingston, RI 02881 USA
[3] Univ Rhode Isl, George & Anne Ryan Inst Neurosci, Kingston, RI 02881 USA
基金
美国国家卫生研究院;
关键词
Antioxidant; Alzheimer's disease (AD); Glycation; Beta amyloid (A beta); Neuroinflammation; Caenorhabditis elegans; ADVANCED GLYCATION ENDPRODUCTS; ALZHEIMERS-DISEASE BRAIN; OXIDATIVE STRESS; NATURAL POLYPHENOLS; PROTEIN; NEUROINFLAMMATION; DYSFUNCTION; ALDEHYDES; INHIBIT; EXTRACT;
D O I
10.1016/j.neuint.2016.09.014
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
Medicinal plants are promising candidates for Alzheimer's disease (AD) research but there is lack of systematic algorithms and procedures to guide their selection and evaluation. Herein, we developed a Neuroprotective Potential Algorithm (NPA) by evaluating twenty-three standardized and chemically characterized Ayurvedic medicinal plant extracts in a panel of bioassays targeting oxidative stress, carbonyl stress, protein glycation, amyloid beta (A beta) fibrillation, acetylcholinesterase (AChE) inhibition, and neuroinflammation. The twenty-three herbal extracts were initially evaluated for: 1) total poly phenol content (Folin-Ciocalteu assay), 2) free radical scavenging capacity (DPPH assay), 3) ferric reducing antioxidant power (FRAP assay), 4) reactive carbonyl species scavenging capacity (methylglyoxal trapping assay), 5) anti-glycative effects (BSA-fructose, and BSA-methylglyoxal assays) and, 6) anti-A(3 fibrillation effects (thioflavin-T assay). Based on assigned index scores from the initial screening, twelve extracts with a cumulative NPA score >= 40 were selected for further evaluation for their: 1) inhibitory effects on AChE activity, 2) in vitro anti-inflammatory effects on murine BV-2 microglial cells (Griess assay measuring levels of lipopolysaccharide-induced nitric oxide species), and 3) in vivo neuroprotective effects on Caenorhabditis elegans post induction of A beta(1-42) induced neurotoxicity and paralysis. Among these, four extracts had a cumulative NPA score >= 60 including Phyllanthus emblica (amla; Indian gooseberry), Mucuna pruriens (velvet bean), Punica granatum (pomegranate) and Curcuma longa (turmeric; curcumin). These extracts also, showed protective effects on H2O2 induced cytotoxicity in differentiated cholinergic human neuronal SH-SY5Y and murine BV-2 microglial cells and reduced tau protein levels in the SH-SY5Y neuronal cells. While published animal data support the neuroprotective effects of several of these Ayurvedic medicinal plant extracts, some remain unexplored for their anti-AD potential. Therefore, the NPA may be utilized, in part, as a strategy to help guide the selection of promising medicinal plant candidates for future AD-based research using animal models. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:164 / 177
页数:14
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