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1.
J Lipid Res ; 54(1): 85-96, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23081987

RESUMO

A high-fat diet (HFD) is a well-known contributing factor in the development of obesity. Most rats fed HFDs become obese. Those that avoid obesity when fed HFDs are considered diet resistant (DR). We performed a microarray screen to identify genes specific to the mesenteric fat of DR rats and revealed high expression of guanylin and guanylyl cyclase C (GC-C) in some subjects. Our histologic studies revealed that the cellular source of guanylin and GC-C is macrophages. Therefore, we developed double-transgenic (Tg) rats overexpressing guanylin and GC-C in macrophages and found that they were resistant to the effects of HFDs. In the mesenteric fat of HFD-fed Tg rats, Fas and perilipin mRNAs were downregulated, and those of genes involved in fatty acid oxidation were upregulated, compared with the levels in HFD-fed wild-type rats. In vitro studies demonstrated that lipid accumulation was markedly inhibited in adipocytes cocultured with macrophages expressing guanylin and GC-C and that this inhibition was reduced after treatment with guanylin- and GC-C-specific siRNAs. Our results suggest that the macrophagic guanylin-GC-C system contributes to the altered expression of genes involved in lipid metabolism, leading to resistance to obesity.


Assuntos
Dieta Hiperlipídica/efeitos adversos , Hormônios Gastrointestinais/metabolismo , Macrófagos/metabolismo , Mesentério/citologia , Peptídeos Natriuréticos/metabolismo , Receptores Acoplados a Guanilato Ciclase/metabolismo , Receptores de Peptídeos/metabolismo , Adipócitos/metabolismo , Animais , Colesterol/sangue , Ácidos Graxos não Esterificados/sangue , Hormônios Gastrointestinais/deficiência , Hormônios Gastrointestinais/genética , Regulação da Expressão Gênica , Técnicas de Introdução de Genes , Insulina/sangue , Fígado/metabolismo , Macrófagos/enzimologia , Macrófagos Peritoneais/enzimologia , Macrófagos Peritoneais/metabolismo , Masculino , Peptídeos Natriuréticos/deficiência , Peptídeos Natriuréticos/genética , Oxirredução , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , RNA Interferente Pequeno/genética , Ratos , Ratos Transgênicos , Receptores de Enterotoxina , Receptores Acoplados a Guanilato Ciclase/deficiência , Receptores Acoplados a Guanilato Ciclase/genética , Receptores de Peptídeos/deficiência , Receptores de Peptídeos/genética , Triglicerídeos/sangue , Triglicerídeos/metabolismo
2.
Eur Neurol ; 65(3): 138-43, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21358203

RESUMO

BACKGROUND: The data on cerebrospinal fluid (CSF) levels of neurotrophins (NTs) in patients with meningoencephalitis are scarce, especially in adult patients. METHODS: We measured CSF levels of NTs such as nerve growth factor (NGF), brain-derived neurotrophic factor, and neurotrophin-3 (NT-3) in adult patients with various meningitis (n = 10) and encephalitis (n = 10) in both acute phase and recovery phase and adult control subjects (n = 21) by the enzyme-linked immunosorbent assay for NTs. RESULTS: Data show that NGF and NT-3 CSF levels were markedly elevated in the patient group in the acute phase compared with non-neurological controls (p < 0.001 and p < 0.05, respectively) and later returned to the levels of controls. Most intriguingly, we only recognized a significant correlation between NGF and NT-3 CSF levels in the patients in the acute phase. CONCLUSION: Such strong correlation of NGF and NT-3 CSF levels strongly suggests that in adult patients, some common regulatory mechanism(s) might be present among various kinds of NTs to cope with central nervous system infection.


Assuntos
Fator Neurotrófico Derivado do Encéfalo/líquido cefalorraquidiano , Encefalite/líquido cefalorraquidiano , Meningites Bacterianas/líquido cefalorraquidiano , Meningite Viral/líquido cefalorraquidiano , Fator de Crescimento Neural/líquido cefalorraquidiano , Neurotrofina 3/líquido cefalorraquidiano , Adolescente , Adulto , Idoso , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Masculino , Pessoa de Meia-Idade
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