Modulation of hepatic microsomal triglyceride transfer protein (MTP) induced by S-nitroso-N-acetylcysteine in ob/ob mice

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3062569 12 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Modulation of hepatic microsomal triglyceride transfer protein (MTP) induced by S-nitroso-N-acetylcysteine in ob/ob mice
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
We evaluated the effects of a potent NO donor, S-nitroso-N-acetylcysteine (SNAC), on microsomal triglyceride transfer protein (MTP) expression in ob/ob mice. NAFLD was induced in male ob/ob mice using a methionine-choline deficient diet (MCD) concomitantly with oral SNAC fed solution (n = 5) or vehicle (control; n = 5) by gavage daily for 4 weeks. Livers were collected for histology and for assessing MTP by RT-qPCR, Western blot, immunohistochemistry and immunogold electron microscopy analyses. Histological analysis showed diffuse macro and microvesicular steatosis, moderate hepatocellular ballooning and moderate inflammatory infiltrate in ob/ob mice fed the MCD diet. With SNAC, mice showed a marked reduction in liver steatosis (p < 0.01), in parenchymal inflammation (p = 0.02) and in MTP protein immunoexpression in zone III (p = 0.05). Moreover, SNAC caused reduction of MTP protein in Western blot analysis (p < 0.05). In contrast, MTP mRNA content was significantly higher (p < 0.05) in mice receiving SNAC. Immuno-electron microscopy showed MTP localized in the rough endoplasmic reticulum of hepatocytes in both treated and untreated groups. However with SNAC treatment, MTP was also observed surrounding fat globules. Histological improvement mediated by a nitric oxide donor is associated with significantly altered expression and distribution of MTP in this animal model of fatty liver disease. Further studies are in progress to examine possible mechanisms and to develop SNAC as a possible therapy for human fatty liver disease. © 2007 Elsevier Inc. All rights reserved.
Έτος δημοσίευσης:
2007
Συγγραφείς:
Oliveira, C.P.M.S.
Alves, V.A.F.
Lima, V.M.R.
Stefano, J.T.
Debbas, V.
Sá, S.V.
Wakamatsu, A.
Corrêa-Giannella, M.L.
de Mello, E.S.
Havaki, S.
Tiniakos, D.G.
Marinos, E.
de Oliveira, M.G.
Giannella-Neto, D.
Laurindo, F.R.
Caldwell, S.
Carrilho, F.J.
Περιοδικό:
Biochemical Pharmacology
Τόμος:
74
Αριθμός / τεύχος:
2
Σελίδες:
290-297
Λέξεις-κλειδιά:
choline; methionine; microsomal triglyceride transfer protein; n acetyl s nitrosocysteine; nitric oxide donor; unclassified drug, animal cell; animal experiment; animal model; animal tissue; article; controlled study; fatty liver; immunoelectron microscopy; immunogold electron microscopy; immunohistochemistry; inflammatory infiltrate; liver cell; liver histology; male; mouse; mouse strain; nonhuman; priority journal; protein expression; reverse transcription polymerase chain reaction; rough endoplasmic reticulum; Western blotting, Acetylcysteine; Animals; Carrier Proteins; Fatty Liver; Liver; Male; Mice; Mice, Obese; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger
Επίσημο URL (Εκδότης):
DOI:
10.1016/j.bcp.2007.04.013
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