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1.
QJM ; 109(12): 785-790, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27256459

RESUMO

BACKGROUND: The purpose of this study was to determine whether irisin is secreted by gastric tumor cells experimentally induced in mice, and also if it has any effect on cancer cachexia. DESIGN AND METHODS: 12 out of 60 BALB/c mice were used as a control group, while N-nitroso-N-methylurea (MNU) was administered orally to the remaining 48. After 150 days, the surviving mice were sacrificed by decapitation, blood and stomach, skeletal muscle, brown and white adipose tissue specimens were collected. Following histopathological evaluation of the stomach tissues, it was decided to create four groups, one control group and three consisting of mice administered MNU, no cancer, pre-cancer and cancer. Gene expression analyses of fibronectin type III domain containing protein 5 (FNDC5) and some cachexia-related proteins were performed in tissue samples, while levels of irisin, and various inflammatory and tumor markers together with cachectic factors were determined in serum samples. RESULTS: The levels of inflammatory, tumor markers and cachectic factors in serum samples were significantly higher in the cancer group compared with the control group. No expression of FNDC5 or zinc-α-2 glycoprotein, a cachectic factor, was observed in gastric tissues from the control and MNU groups, whereas significantly increased FNDC5 expression was determined in the both white and brown adipose tissues from the cancer group. CONCLUSION: Increased FNDC5 expression in white and brown adipose tissues may have a cachectic effect in mice with induced cancer. However, it is not possible to explain the mechanism of the relationship between irisin and gastric cancer development on the basis of the results of this study.


Assuntos
Tecido Adiposo Marrom/metabolismo , Tecido Adiposo Branco/metabolismo , Caquexia/metabolismo , Fibronectinas/metabolismo , Neoplasias Gástricas/metabolismo , Animais , Biomarcadores Tumorais/genética , Biomarcadores Tumorais/metabolismo , Modelos Animais de Doenças , Fibronectinas/genética , Humanos , Camundongos , Camundongos Endogâmicos BALB C , Monocinas/genética , Monocinas/metabolismo , RNA Mensageiro/genética , Distribuição Aleatória , Neoplasias Gástricas/genética
2.
Clin Biochem ; 44(17-18): 1385-9, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21986594

RESUMO

OBJECTIVES: To investigate the relationship between carbonic anhydrase (CA) II autoantibody and lipid peroxidation, certain antioxidant parameters, and cytokines in rheumatoid arthritis (RA) patients. DESIGN AND METHODS: Serum levels of CA II autoantibody, cytokines (TNFα, IL-6, IFN-γ, IL-1ß) and bone markers (crosslaps, osteocalcine) and erythrocyte levels of antioxidant enzyme activities (SOD, CAT, GPx), GSH and MDA, and CA activities were measured in RA patients and healthy controls. RESULTS: The CA II autoantibody titers were significantly higher (P<0.05), and erythrocyte SOD activities were significantly lower (P<0.05) in RA patients. A significant negative correlation between CA II autoantibody titers and SOD activities in RA group was established (r=-0.430, p=0.006). The elevated cytokine levels could not be correlated with CA II autoantibody levels in RA. CONCLUSION: These results suggest that increased erythrocyte oxidative stress observed in RA may be effective in the mechanism of CA II autoantibody formation.


Assuntos
Artrite Reumatoide/sangue , Autoanticorpos/sangue , Anidrase Carbônica II/imunologia , Estresse Oxidativo , Superóxido Dismutase/sangue , Adulto , Artrite Reumatoide/imunologia , Artrite Reumatoide/fisiopatologia , Biomarcadores/sangue , Anidrase Carbônica II/sangue , Estudos de Casos e Controles , Catalase/sangue , Colágeno/sangue , Citocinas/sangue , Eritrócitos/enzimologia , Feminino , Glutationa/sangue , Glutationa Peroxidase/sangue , Humanos , Masculino , Malondialdeído/sangue , Pessoa de Meia-Idade , Osteocalcina/sangue , Fragmentos de Peptídeos/sangue
3.
J Enzyme Inhib Med Chem ; 19(3): 279-81, 2004 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15500001

RESUMO

Studies on the biochemical and molecular mechanisms underlying obesity have shown that the expression of some proteins was decreased with obesity in rat adipose tissue. One of these proteins is carbonic anhydrase III (CA III) which constitutes 24% of the cytosolic protein content and its function is unclear. A freshly isolated rat adipose cell culture model was used to examine the effect of leptin and insulin on CA III expression. It was found that leptin decreased CA III expression while insulin increased it which suggests that the decrease in CA III expression observed in obesity in rat adipose tissue may be related to hyperleptinemia.


Assuntos
Tecido Adiposo/efeitos dos fármacos , Anidrase Carbônica III/genética , Regulação da Expressão Gênica/efeitos dos fármacos , Insulina/farmacologia , Leptina/farmacologia , Tecido Adiposo/enzimologia , Tecido Adiposo/metabolismo , Animais , Células Cultivadas , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Ratos , Ratos Sprague-Dawley
4.
J Enzyme Inhib Med Chem ; 19(2): 181-4, 2004 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15449734

RESUMO

It is well known that the role of leptin in the body is to regulate food intake and energy expenditure but the process of leptin secretion by adipose tissue and the components involved in this process are still obscure. Carbonic anhydrase III (CA III) is the most abundant protein of the rat adipose tissue and its amount decreases with obesity. The effect of the inhibition of CA III on leptin secretion by rat epididymal adipose tissue was examined. Dorzolamide, a CA inhibitor, caused a decrease in dexamethasone and insulin-induced leptin secretion suggesting a possible role for CA III in the mechanism of leptin secretion.


Assuntos
Tecido Adiposo/metabolismo , Anidrase Carbônica III/antagonistas & inibidores , Inibidores Enzimáticos/farmacologia , Leptina/metabolismo , Sulfonamidas/farmacologia , Tiofenos/farmacologia , Tecido Adiposo/efeitos dos fármacos , Tecido Adiposo/enzimologia , Animais , Dexametasona/farmacologia , Epididimo , Insulina/farmacologia , Masculino , Ratos , Ratos Sprague-Dawley
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