Protective effects of chlorogenic acid in 3-nitropropionic acid induced toxicity and genotoxicity

被引:17
|
作者
Alarcon-Herrera, Norberto [1 ]
Flores-Maya, Saul [1 ]
Bellido, Belen [2 ]
Garcia-Bores, Ana M. [3 ]
Mendoza, Ernesto [2 ]
Avila-Acevedo, Guillermo [3 ]
Hernandez-Echeagaray, Elizabeth [2 ]
机构
[1] Univ Nacl Autonoma Mexico, FES Iztacala, UBIPRO, Lab Recursos Nat, Mexico City, DF, Mexico
[2] Univ Nacl Autonoma Mexico, FES Iztacala, Lab Neurofisiol Desarrollo & Neurodegenerac UBIME, Mexico City, DF, Mexico
[3] Univ Nacl Autonoma Mexico, FES Iztacala, UBIPRO, Lab Fitoquim, Mexico City, DF, Mexico
关键词
Mitochondria; Antioxidants; Polyphenols; Caffeoyl; Neurotoxins; Micronuclei; INDUCED STRIATAL TOXICITY; CAFFEIC ACID; PHENOLIC-COMPOUNDS; ERYTHROCYTE MICRONUCLEUS; SUCCINATE-DEHYDROGENASE; ANTIOXIDANT PROPERTIES; HYDROXYCINNAMIC ACIDS; IN-VITRO; RATS; INHIBITION;
D O I
10.1016/j.fct.2017.04.048
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Mitochondrial inhibition with the toxin 3-Nitropropionic acid (3-NP) has been used to study the underlying mechanisms in striatal neurodegeneration, but few experiments have evaluated its toxicity and genotoxicity of in vivo administration. Furthermore, different antioxidant molecules may prevent degeneration induced by the toxic effects of 3-NP. Therefore, the purpose of this study was to evaluate the toxicity and genotoxicity induced by 3-NP (15 mg/kg) in the micronuclei assay method; also, we assessed chlorogenic acid (CGA, 100 mg/kg) for its anti-toxic and anti-genotoxic effect in damage produced by in vivo treatment with 3-NP. 3-NP induced toxicity and genotoxicity. CGA administered as a co-treatment with 3-NP (3-NP + CA) reduced toxicity by 32.76%, as a pre-treatment for 5 days only, followed by 3-NP treatment (P/CA, 3-NP) inhibiting toxicity by 24.04%, or as a pre-treatment, plus a co-treatment with 3-NP (P/CA, 3-NP + CA) avoided any toxic effect. CGA alone did not exhibit any toxic effect. Only P/CGA, 3-NP + CGA group, avoided toxicity and genotoxicity, suggesting that CGA could be suitable to prevent, reduce or delay toxicity and cell death. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1018 / 1025
页数:8
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