Neuroprotective Effects of Acai (Euterpe oleracea Mart.) against Rotenone In Vitro Exposure

被引:42
|
作者
Machado, Alencar Kolinski [1 ,2 ]
Andreazza, Ana Cristina [3 ,4 ]
da Silva, Tatiane Morgana [5 ]
Boligon, Aline Augusti [6 ]
do Nascimento, Vanusa [2 ,7 ]
Scola, Gustavo [3 ,4 ]
Duong, Angela [3 ]
Cadona, Francine Carla [2 ,8 ]
Ribeiro, Euler Esteves [2 ,7 ]
Manica da Cruz, Ivana Beatrice [1 ,2 ,8 ]
机构
[1] Univ Fed Santa Maria, Postgrad Program Pharmacol, Santa Maria, RS, Brazil
[2] Univ Fed Santa Maria, Dept Morphol, Hlth Sci Ctr, Biogen Lab, Santa Maria, RS, Brazil
[3] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[4] Ctr Addict & Mental Hlth, Toronto, ON, Canada
[5] Univ Fed Pelotas, Pelotas, RS, Brazil
[6] Univ Fed Santa Maria, Dept Ind Pharm, Phytochem Res Lab, Santa Maria, RS, Brazil
[7] Univ Amazonas State, Age Open Univ 3, Manaus, Amazonas, Brazil
[8] Univ Fed Santa Maria, Postgrad Program Biol Sci, Toxicol Biochem, Santa Maria, RS, Brazil
关键词
MITOCHONDRIAL COMPLEX I; AMAZONIAN PALM BERRY; BIPOLAR DISORDER; NEURODEGENERATIVE DISEASES; PREFRONTAL CORTEX; OXIDATIVE STRESS; FREE-RADICALS; ANTIOXIDANT; LITHIUM; FRUIT;
D O I
10.1155/2016/8940850
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neuropsychiatric diseases, such as bipolar disorder (BD) and schizophrenia (SCZ), have a very complex pathophysiology. Several current studies describe an association between psychiatric illness and mitochondrial dysfunction and consequent cellular modifications, including lipid, protein, and DNA damage, caused by cellular oxidative stress. Euterpe oleracea (acai) is a powerful antioxidant fruit. Acai is an Amazonian palm fruit primarily found in the lowlands of the Amazonian rainforest, particularly in the floodplains of the Amazon River. Given this proposed association, this study analyzed the potential in vitro neuropharmacological effect of Euterpe oleracea (acai) extract in the modulation of mitochondrial function and oxidative metabolism. SH-SY5Y cells were treated with rotenone to inducemitochondrial complex I dysfunction and before and after we exposed the cells to acai extract at 5 mu g/mL. Treated and untreated cells were then analyzed by spectrophotometric, fluorescent, immunological, and molecular assays. The results showed that acai extract can potentially increase protein amount and enzyme activity of mitochondrial complex I, mainly through NDUFS7 and NDUFS8 overexpression. Acai extract was also able to decrease cell reactive oxygen species levels and lipid peroxidation. We thus suggest acai as a potential candidate for drug development and a possible alternative BD therapy.
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页数:14
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