Biophenols: Enzymes (β-secretase, Cholinesterases, histone deacetylase and tyrosinase) inhibitors from olive (Olea europaea L.)

被引:64
|
作者
Omar, Syed Haris [1 ,2 ]
Scott, Christopher J. [1 ,2 ]
Hamlin, Adam S. [3 ]
Obied, Hassan K. [1 ,2 ]
机构
[1] Charles Sturt Univ, Fac Sci, Sch Biomed Sci, Wagga Wagga, NSW 2678, Australia
[2] Charles Sturt Univ, Graham Ctr Agr Innovat, Wagga Wagga, NSW 2678, Australia
[3] Univ New England, Sch Sci & Technol, Armidale, NSW 2351, Australia
关键词
Olive biophenols; BACE-1; AChE & BChE; HDAC; SH-SY5Y cells; Verbascoside; Rutin; Alzheimer's disease; AMYLOID PRECURSOR PROTEIN; ALZHEIMERS-DISEASE; L-DOPA; ANTIOXIDANT ACTIVITY; MUSHROOM TYROSINASE; PARKINSONS-DISEASE; TOXICITY; ACID; ACETYLATION; FLAVONOIDS;
D O I
10.1016/j.fitote.2018.05.011
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The focus of this study was on inhibition of enzymes involved in the pathogenesis Alzheimer's disease (AD) including prime amyloid beta (A beta) producing enzyme (beta-secretase: BACE-1) and disease progression enzymes including acetylcholinesterase (AChE), butyrylcholinesterase (BChE), histone deacetylase (HDAC), and tyrosinase along with the catecholamine L-DOPA, by using olive biophenols. Here we report the strongest inhibition of BACE-1 from rutin (IC50: 3.8 nM) followed by verbascoside (IC50: 6.3 nM) and olive fruit extract (IC50: 18 ng), respectively. Olive biophenol, quercetin exhibited strongest enzyme inhibitory activity against tyrosinase (IC50: 10.73 mu M), BChE (IC50: 19.08 mu M), AChE (IC50: 55.44 mu M), and HDAC (IC50: 105.1 mu M) enzymes. Furthermore, olive biophenol verbascoside (IC50: 188.6 mu M), and hydroxytyrosol extreme extract (IC50: 66.22 mu g) were showed the highest levels of inhibition against the HDAC enzyme. Neuroprotective capacity against levodopa-induced toxicity in neuroblastoma (SH-SY5Y) cells of olive biophenols were assessed, where rutin indicated the highest neuroprotection (74%), followed by caffeic acid (73%), and extract hydroxytyrosol extreme (97%), respectively. To the best of our knowledge, this is the first in vitro report on the enzymes inhibitory activity of olive biophenols. Taken together, our in vitro results data suggest that olive biophenols could be a promising natural inhibitor, which may reduce the enzyme-induced toxicity associated with the oxidative stress involved in the progression of AD. Chemical compounds used in the study: Acetylthiocholine iodide (PubChem CID: 74629); S-Butyrylthiocholine chloride (PubChem CID: 3015121); Caffeic acid (PubChem CID: 689043); Dimethyl sulfoxide (DMSO) (PubChem: 679); L-3,4-Dihydroxyphenylalanine (L-DOPA) (PubChem CID: 6047); 5,5'-Dithiobis (2-nitrobenzoic acid) (DTNB) (PubChem CID: 6254); Epigallocatechin gallate (EGCG) (PubChem CID: 65064); Ethylenediamine tetraacetic acid (EDTA) (PubChem CID: 6049); Galantamine hydrobromide (PubChem CID: 121587); L-Glutamine (PubChem CID: 5961); Hydroxytyrosol (PubChem CID: 82755); Kojic acid (PubChem CID: 3840); Luteolin (PubChem CID: 5280445); Oleuropein (PubChem CID: 5281544); Penicillin-streptomycin (PubChem CID: 131715954); Quercetin (PubChem CID: 5280343); Rutin (PubChem CID: 5280805); Tris-HCI buffer (PubChem: 93573); Trypan blue (PubChem: 9562061).
引用
收藏
页码:118 / 129
页数:12
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