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1.
Eur J Neurol ; 15(9): 998-1001, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18637954

RESUMO

BACKGROUND AND PURPOSE: In recent years, different approaches have been used to investigate changes of cerebrospinal fluid (CSF) proteome in patients affected by multiple sclerosis (MS) with the aim to identify protein markers with potential diagnostic or prognostic value. Because of the lack of standardization of current proteomic techniques, contrasting results were achieved until now in different laboratories. In this study, we compare CSF proteome of 10 relapsing-remitting MS (RR-MS) patients, 11 patients with clinically isolated syndrome (CIS), and 10 control subjects without neurological or systemic diseases. METHODS: The differential expression of CSF proteins amongst these cohorts of patients was investigated by using two-dimensional electrophoresis and mass spectrometry. RESULTS AND CONCLUSIONS: We found an overexpression of IgG free kappa light chain protein in both CIS and RR-MS patients, compared with control subjects and an increased expression of an apolipoprotein E isoform in RR-MS patients, compared with CIS and control groups. Our results confirm the presence of CSF proteome changes in MS patients. Future research should be aimed to investigate the role of these candidate CSF markers in larger cohorts of CIS and MS patients.


Assuntos
Proteínas do Líquido Cefalorraquidiano/análise , Eletroforese em Gel Bidimensional , Cadeias kappa de Imunoglobulina/líquido cefalorraquidiano , Doenças do Sistema Nervoso/líquido cefalorraquidiano , Proteômica , Apolipoproteína A-I/líquido cefalorraquidiano , Apolipoproteínas E/líquido cefalorraquidiano , Biomarcadores/líquido cefalorraquidiano , Estudos de Coortes , Humanos , Esclerose Múltipla Recidivante-Remitente/líquido cefalorraquidiano , Pré-Albumina/líquido cefalorraquidiano
2.
J Lipid Res ; 45(2): 308-16, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-14563831

RESUMO

Fatty acid synthetase (FAS) is overexpressed in various tumor tissues, and its inhibition and/or malonyl-CoA accumulation have been correlated to apoptosis of tumor cells. It is widely recognized that both omega-3 and omega-6 polyunsaturated fatty acids (PUFAs) depress FAS expression in liver, although epidemiological and experimental reports attribute antitumor properties only to omega-3 PUFA. Therefore, we investigated whether lipogenic gene expression in tumor cells is differently regulated by omega-6 and omega-3 PUFAs. Morris hepatoma 3924A cells were implanted subcutaneously in the hind legs of ACI/T rats preconditioned with high-lipid diets enriched with linoleic acid or alpha-linolenic acid. Both-high lipid diets depressed the expression of FAS and acetyl-CoA carboxylase in tumor tissue, this effect correlating with a decrease in the mRNA level of their common sterol regulatory element binding protein-1 transcription factor. Hepatoma cells grown in rats on either diet did not accumulate malonyl-CoA. Apoptosis of hepatoma cells was induced by the alpha-linolenic acid-enriched diet but not by the linoleic acid-enriched diet. Therefore, in this experimental model, apoptosis is apparently independent of the inhibition of fatty acid synthesis and of malonyl-CoA cytotoxicity. Conversely, it was observed that apoptosis induced by the alpha-linolenic acid-enriched diet correlated with a decrease in arachidonate content in hepatoma cells and decreased cyclooxygenase-2 expression.


Assuntos
Apoptose/efeitos dos fármacos , Regulação Neoplásica da Expressão Gênica/efeitos dos fármacos , Isoenzimas/genética , Neoplasias Hepáticas Experimentais/patologia , Prostaglandina-Endoperóxido Sintases/genética , Ácido alfa-Linolênico/administração & dosagem , Acetil-CoA Carboxilase/genética , Acetil-CoA Carboxilase/metabolismo , Animais , Apoptose/genética , Proteínas Estimuladoras de Ligação a CCAAT/genética , Ciclo-Oxigenase 2 , Dieta , Gorduras Insaturadas na Dieta , Regulação para Baixo/genética , Ácido Graxo Sintases/genética , Ácido Graxo Sintases/metabolismo , Ácidos Graxos Ômega-6/genética , Ácidos Graxos Ômega-6/metabolismo , Ácidos Graxos Insaturados/genética , Ácidos Graxos Insaturados/metabolismo , Isoenzimas/biossíntese , Neoplasias Hepáticas Experimentais/tratamento farmacológico , Neoplasias Hepáticas Experimentais/genética , Neoplasias Hepáticas Experimentais/metabolismo , Prostaglandina-Endoperóxido Sintases/biossíntese , Ratos , Ácido alfa-Linolênico/metabolismo
3.
J Lipid Res ; 44(4): 696-704, 2003 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-12562863

RESUMO

The hindlimb-suspended rat was used as animal model to investigate the effects induced by immobilization of the skeletal muscle in the expression of the genes encoding hepatic lipogenic enzymes. Following a 14-day period of immobilization, rats were injected intraperitoneally with radioactive acetate, and the labeling of hepatic lipids and cholesterol was evaluated 15 min after the isotope injection. The incorporation of labeled acetate in lipids and cholesterol was almost three times higher in the liver of immobilized rats than in control animals as a consequence of the enhanced transcription of the genes encoding acetyl-CoA synthase, acetyl-CoA carboxylase, fatty acid synthase, and 3-hydroxy-3-methylglutaryl-CoA reductase. The high expression of the key enzymes for fatty acid and cholesterol synthesis induced by immobilization was not paralleled by an increase of the hepatic sterol-regulatory element binding protein (SREBP)-1 and SREBP-2 mRNA content. However, the expression of the mature form of SREBP-1 and SREBP-2 was higher in the nuclear fraction of immobilized rat liver than in controls due to a significant increase of the cleavage of the native proteins. Immobilization also affected the expression of proteins involved in lipid degradation. In fact, the hepatic content of peroxisome proliferator-activated receptor-alpha (PPARalpha) mRNA and of PPARalpha target genes encoding carnitine palmitoyl transferase-1 and acyl-CoA oxidase were significantly increased upon immobilization.


Assuntos
Imobilização/fisiologia , Lipídeos/biossíntese , Fígado/enzimologia , Acetatos/metabolismo , Animais , Proteínas Estimuladoras de Ligação a CCAAT/análise , Colesterol/biossíntese , Proteínas de Ligação a DNA/análise , Enzimas/genética , Lipídeos/análise , Fígado/química , Masculino , Modelos Animais , RNA Mensageiro/análise , Ratos , Ratos Wistar , Proteína de Ligação a Elemento Regulador de Esterol 1 , Fatores de Transcrição/análise
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