Chemoprotective effects of Ulva lactuca (green seaweed) aqueous-ethanolic extract against subchronic exposure to benzo(a)pyrene by CYP1A1 inhibition in mice

被引:8
作者
Delgado-Roche, Livan [1 ,2 ]
Rodeiro, Idania [1 ]
Riera, Mario [1 ]
Alfredo Herrera, Jose [3 ]
Venturi, Ivonilce [4 ]
Hernandez, Yasnay [1 ]
Fernandez, Gisselle [5 ]
Luis Perez, Carlos [5 ]
Carlos Rodriguez, Juan [6 ]
David Fernandez, Miguel [1 ]
Hernandez-Balmaseda, Ivones [1 ]
Raul Fernandez, Julio [7 ]
Mesta, Fernando [8 ]
Paz, Miriam Teresa [9 ]
机构
[1] Inst Marine Sci ICIMAR, Dept Pharmacol, Loma 14,Plaza Revoluc,PO 10600, Havana, Cuba
[2] Ctr AF Technol Studies CAFET, Carnot Lab, Mexico City, DF, Mexico
[3] Havana Univ, Inst Mat Sci & Technol IMRE, Havana, Cuba
[4] Univ Vale Itajai, Programa Posgrad Ciencias Farmaceut, Itajai, SC, Brazil
[5] Med Univ Havana UCMH, Inst Basic & Preclin Sci Victoria de Giron ICBP, Havana, Cuba
[6] Natl Inst Oncol & Radiobiol, Dept Pathol, Havana, Cuba
[7] Ctr Genet Engn & Biotechnol, Dept Genom, Havana, Cuba
[8] Inst Politecn Nacl, Escuela Nacl Med & Homeopatia, Mexico City, DF, Mexico
[9] Fed Univ Minas Gerais UFMG, Inst Biol Sci ICB, Dept Pharmacol, Ave Antonio Carlos 6627, Belo Horizonte, MG, Brazil
关键词
antigenotoxic; benzo(a)pyrene; chemoprotection; CYP1A1; green alga; Ulva lactuca; HYDROCARBON-DNA-ADDUCTS; ANTIOXIDANT STATUS; FASCIATA DELILE; MARINE-ALGAE; LUNG; EXPRESSION; CARCINOGENESIS; PREVENTION; BIOMARKERS; TISSUES;
D O I
10.1002/ptr.6289
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The protective effect of the supplementation with an aqueous-ethanolic extract obtained from Ulva lactuca (Delile) green seaweed on benzo[a] pyrene-induced damage in mice was evaluated. Animals were treated with oral doses of U.lactuca extract (100 and 400mg/kg) for 9weeks. They were exposed to 50mg/kg of oral doses of benzo(a)pyrene starting from the second week and up to the fifth week. Groups treated with benzo(a)pyrene only (second to fifth weeks), sunflower oil (vehicle, 9weeks), or U.lactuca extract (100 and 400mg/kg, 9weeks) were also included in the study. The treatment with 400mg/kg of the extract ameliorated the oxidative damage, decreased IL-1 and TNF- levels, and favorably regulated the antioxidant defenses compared with benzo(a)pyrene-exposed group. The benzo(a)pyrene-induced DNA damage was also reduced, as it was evidenced by the lower micronucleus formation in U.lactuca extract-supplemented animals. The extract protected the hepatic tissue, and it reduced the liver activity/expression of CYP1A1. These results altogether suggested a chemoprotective effect of U.lactuca extract against benzo(a)pyrene-induced-toxicity in mice, probably associated with an inhibitory effect of carcinogen bioactivation.
引用
收藏
页码:958 / 967
页数:10
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