Abstract |
Cancer cachexia is a syndrome that causes profound metabolic disruption. Lipid metabolism in the liver is markedly affected. We investigated the effect of cachexia upon liver-acinus lipid-metabolism zonation in Walker 245 carcinosarcoma-bearing rats (TB). The expression of protein (by Western blotting) and mRNA (by semi-quantitative polymerase chain reaction) of the enzymes of the carnitine palmitoyltransferase system ( CPT I and CPT II) and of liver fatty-acid-binding protein (L-FABP) was studied. Although no changes were found for these parameters, the maximal activities (by radioassay) of CPT I and II were reduced (P<0.05) in TB compared with controls. CPT II activity in the perivenous (PV) region was higher in TB compared with controls. The distribution of CPT II and L-FABP (by immunohistochemistry) within the acinus was modified by cachexia: whereas CPT II positivity was restricted to the PV zone, L-FABP labelling shifted from periportal (control) to perivenous (TB) zone. These changes in metabolic zonation, together with decreased CPT II activity, may contribute to the aggravation of cachexia.
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Authors | Melissa Kazantzis, Marília C L Seelaender |
Journal | Cell and tissue research
(Cell Tissue Res)
Vol. 321
Issue 3
Pg. 419-27
(Sep 2005)
ISSN: 0302-766X [Print] Germany |
PMID | 16021474
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Carrier Proteins
- Fabp1 protein, rat
- Fatty Acid-Binding Proteins
- RNA, Messenger
- Carnitine O-Palmitoyltransferase
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Topics |
- Animals
- Cachexia
(metabolism)
- Carcinoma 256, Walker
(physiopathology)
- Carnitine O-Palmitoyltransferase
(genetics, metabolism)
- Carrier Proteins
(genetics, metabolism)
- Fatty Acid-Binding Proteins
- Gene Expression Regulation
- Hepatocytes
(cytology, enzymology)
- Immunohistochemistry
- Lipid Metabolism
- Liver
(cytology, enzymology)
- Male
- RNA, Messenger
(metabolism)
- Rats
- Rats, Wistar
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