Inhibition of glutathione S-transferase P type-positive foci development by linolic acid hydroperoxides and their secondary oxidative products in a rat in vivo mid-term test for liver carcinogens.

Abstract:

:The effects of linolic acid hydroperoxides (product A) and secondary oxidative products of product A (product B), were examined in an in vivo mid-term test for hepatocarcinogens or hepatopromoters in rats. The number of placental type of glutathione S-transferase (GST-P)-positive foci of the liver was significantly reduced in rats given diethylnitrosamine (DEN) followed by products A (4.64 +/- 1.09, P less than 0.05) or B (3.62 +/- 1.65, P less than 0.01) as compared to the controls given carcinogen alone (6.31 +/- 2.82). The area of GST-P positive foci was also significantly reduced in rats given DEN followed by product B (0.30 +/- 0.21, P less than 0.05) as compared to the controls (0.47 +/- 0.23). These results suggest that linolic acid hydroperoxides or their secondary oxidative products are not hepatocarcinogens and rather may possess inhibitory potential for liver carcinogenesis.

journal_name

Toxicol Lett

journal_title

Toxicology letters

authors

Hirose M,Thamavit W,Asamoto M,Osawa T,Ito N

doi

10.1016/0378-4274(86)90048-2

subject

Has Abstract

pub_date

1986-07-01 00:00:00

pages

51-8

issue

1-2

eissn

0378-4274

issn

1879-3169

pii

0378-4274(86)90048-2

journal_volume

32

pub_type

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