Neuroprotective effect of steroidal alkaloids on glutamate-induced toxicity by preserving mitochondrial membrane potential and reducing oxidative stress

被引:56
作者
Taveira, Marcos [1 ]
Sousa, Carla [1 ]
Valentao, Patricia [1 ]
Ferreres, Federico [2 ]
Teixeira, Joao P. [3 ]
Andrade, Paula B. [1 ]
机构
[1] Univ Porto, REQUIMTE Lab Farmacognosia, Dept Quim, Fac Farm, P-4050313 Oporto, Portugal
[2] CEBAS CSIC Res Grp Qual Safety & Bioact Plant Foo, Dept Food Sci & Technol, Murcia 30100, Spain
[3] Natl Inst Hlth, Dept Environm Hlth, P-4000055 Oporto, Portugal
关键词
Steroidal alkaloids; Neuroprotection; Oxidative stress; Mitochondrial membrane potential; Cholinergic receptors; HUMAN NEUROBLASTOMA SH-SY5Y; NICOTINIC ACETYLCHOLINE-RECEPTORS; ALZHEIMERS-DISEASE; INDUCED APOPTOSIS; HUMAN BREAST; CELLS; INHIBITORS; ACID; BUTYRYLCHOLINESTERASE; CHOLINESTERASE;
D O I
10.1016/j.jsbmb.2013.12.013
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
Several evidences suggest that enhanced oxidative stress is involved in the pathogenesis and/or progression of several neurodegenerative diseases. The aim of this study was to investigate for the first time whether both extracts from tomato plant (Lycopersicon esculentum Mill.) leaves and their isolated steroidal alkaloids (tomatine and tomatidine) afford neuroprotective effect against glutamate-induced toxicity in SH-SY5Y neuroblastoma cells and to elucidate the mechanisms underlying this protection. Steroidal alkaloids from tomato are well known for their cholinesterases' inhibitory capacity and the results showed that both purified extracts and isolated compounds, at non-toxic concentrations for gastric (AGS), intestinal (Caco-2) and neuronal (SH-SY5Y) cells, have the capacity to preserve mitochondria membrane potential and to decrease reactive oxygen species levels of SH-SY5Y glutamate-insulted cells. Moreover, the use of specific antagonists of cholinergic receptors allowed observing that tomatine and tomatidine can interact with nicotinic receptors, specifically with the alpha 7 type. No effect on muscarinic receptors was noticed. In addition to the selective cholinesterases' inhibition revealed by the compounds/extracts, these results provide novel and important insights into their neuroprotective mechanism. This work also demystifies the applicability of these compounds in therapeutics, by demonstrating that their toxicity was overestimated for long time. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:106 / 115
页数:10
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