Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/6820
Title: Disruption of sphingolipid biosynthesis in hepatocyte nodules: selective proliferative stimulus induced by fumonisin B1
Authors: van der Westhuizen, L 
Gelderblom, WCA 
Shephard, GS 
Swanevelder, S 
Keywords: Fumonisin;Hepatocyte nodules;Sphingosine;Sphinganine
Issue Date: 2004
Publisher: Elsevier
Source: van der Westhuizen L Gelderblom WCA Shephard GS Swanevelder S, 2004. Disruption of sphingolipid biosynthesis in hepatocyte nodules: selective proliferative stimulus induced by fumonisin B1. Toxicology, 200(1):69-75
Journal: Toxicology, 200(1):69-75 
Abstract: In order to investigate the role of sphingolipid disruption in the cancer promoting potential of fumonisin B(1) (FB(1)) in the development of hepatocyte nodules, male Fischer 344 rats were subjected to cancer initiation (FB(1) containing diet or diethylnitrosamine (DEN) by i.p. injection) and promotion (2-acetylaminofluorene with partial hepatectomy, 2-AAF/PH) treatments followed by a secondary FB(1) dietary regimen. Sphinganine (Sa) and sphingosine (So) levels were measured by high performance liquid chromatography in control, surrounding and nodular liver tissues of the rats. The disruption of sphingolipid biosynthesis by the secondary FB(1) treatment in the control rats was significantly (P < 0.05) enhanced by the 2-AAF/PH cancer promotion treatment. The nodular and surrounding Sa levels returned to baseline following FB(1) initiation and 2-AAF/PH promotion. When comparing the groups subjected to the secondary FB(1) treatment, the initiation effected by FB(1) was less (P < 0.01) sensitive to the accumulation of Sa in the nodular and surrounding tissues than DEN initiation and the 2-AAF/PH control treatment. In contrast, the So level of FB(1) initiation was marginally increased in the nodules compared to the surrounding liver after 2-AAF/PH promotion and significantly (P < 0.05) higher with the secondary FB(1) treatment. Although, the FB(1)-induced hepatocyte nodules were not resistant to the disruption of sphingolipid biosynthesis, the nodular So levels were increased and might provide a selective growth stimulus possibly induced by bio-active sphingoid intermediates such as sphingosine 1-phosphate (S1P).
Description: Article
URI: http://hdl.handle.net/11189/6820
DOI: 10.1016/j.tox.2004.03.011
Appears in Collections:HWSci - Journal Articles (DHET subsidised)

Show full item record

Page view(s)

15
checked on Feb 16, 2019

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons