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

Phytother Res. 2019 Apr;33(4):958-967. doi: 10.1002/ptr.6289. Epub 2019 Feb 6.

Abstract

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 400 mg/kg) for 9 weeks. They were exposed to 50 mg/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, 9 weeks), or U. lactuca extract (100 and 400 mg/kg, 9 weeks) were also included in the study. The treatment with 400 mg/kg of the extract ameliorated the oxidative damage, decreased IL-1β and TNF-α 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.

Keywords: CYP1A1; Ulva lactuca; antigenotoxic; benzo(a)pyrene; chemoprotection; green alga.

MeSH terms

  • Animals
  • Benzo(a)pyrene / toxicity
  • Cytochrome P-450 CYP1A1 / antagonists & inhibitors*
  • Dietary Supplements
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Seaweed*
  • Ulva*

Substances

  • Benzo(a)pyrene
  • Cytochrome P-450 CYP1A1