Changes in GM1 ganglioside content and localization in cholestatic rat liver
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- biologické markery krev MeSH
- cholestáza chemicky indukované metabolismus patologie MeSH
- cholesterol krev MeSH
- ethinylestradiol MeSH
- G(M1) gangliosid metabolismus MeSH
- hepatocyty účinky léků metabolismus patologie MeSH
- játra účinky léků metabolismus patologie MeSH
- krysa rodu Rattus MeSH
- potkani Wistar MeSH
- propylenglykoly farmakologie MeSH
- referenční hodnoty MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biologické markery MeSH
- cholesterol MeSH
- ethinylestradiol MeSH
- G(M1) gangliosid MeSH
- propylenglykoly MeSH
(Glyco)sphingolipids (GSL) are believed to protect the cell against harmful environmental factors by increasing the rigidity of plasma membrane. Marked decrease of membrane fluidity in cholestatic hepatocytes was described but the role of GSL therein has not been investigated so far. In this study, localization in hepatocytes of a representative of GSL, the GM1 ganglioside, was compared between of rats with cholestasis induced by 17alpha-ethinylestradiol (EE) and vehicle propanediol treated or untreated animals. GM1 was monitored by histochemical reaction employing cholera toxin B-subunit. Our findings in normal rat liver tissue showed that GM1 was localized in sinusoidal and canalicular hepatocyte membranes in both peripheral and intermediate zones of the hepatic lobules, and was nearly absent in central zones. On the contrary, in EE-treated animals GM1 was also expressed in central lobular zones. Moreover, detailed densitometry analysis at high magnification showed greater difference of GM1 expression between sinusoidal surface areas and areas of adjacent cytoplasm, caused as well by increased sinusoidal staining in central lobular zone as by decreased staining in cytoplasm in peripheral zone. These differences correlated with serum bile acids as documented by linear regression analyses. Both GM1 content and mRNA corresponding to GM1-synthase remained unchanged in livers; the enhanced expression of GM1 at sinusoidal membrane thus seems to be due to re-distribution of cellular GM1 at limited biosynthesis and could be responsible for protection of hepatocytes against harmful effects of bile acids accumulated during cholestasis.
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Pediatrics. 1981 Apr;67(4):461-6 PubMed
Biochim Biophys Acta. 1992 Dec 11;1113(3-4):339-73 PubMed
Ann Ist Super Sanita. 1988;24(1):23-31 PubMed
Acta Histochem Suppl. 1975;14:129-38 PubMed
Dig Dis Sci. 1999 Aug;44(8):1662-8 PubMed
Ann Hepatol. 2003 Oct-Dec;2(4):150-8 PubMed
Anal Biochem. 1988 Sep;173(2):368-75 PubMed
Biochem Pharmacol. 1995 Oct 12;50(8):1223-32 PubMed
Biochim Biophys Acta. 1981 Oct 2;647(2):196-202 PubMed
J Histochem Cytochem. 1994 Feb;42(2):155-66 PubMed
J Cell Biol. 1997 Apr 21;137(2):347-57 PubMed
Prog Brain Res. 1994;101:XI-XIV PubMed
Biochemistry. 1988 May 31;27(11):3939-46 PubMed
Exp Mol Pathol. 1992 Aug;57(1):47-61 PubMed
J Biol Chem. 2002 Jul 19;277(29):25855-8 PubMed
J Lipid Res. 1972 Sep;13(5):680-6 PubMed
J Neurochem. 1963 Sep;10:613-23 PubMed
FEBS Lett. 2002 Oct 2;529(1):54-9 PubMed
J Lab Clin Med. 1988 Dec;112(6):679-85 PubMed
Biochim Biophys Acta. 1976 Dec 2;455(2):433-51 PubMed
Curr Opin Hematol. 2003 Jan;10(1):16-24 PubMed
J Gastroenterol Hepatol. 2000 Aug;15(8):887-94 PubMed
Lipids. 1977 Jun;12(6):455-68 PubMed
Biomed Chromatogr. 2007 May;21(5):446-50 PubMed
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