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1.
Nutrients ; 12(1)2019 Dec 18.
Artigo em Inglês | MEDLINE | ID: mdl-31861497

RESUMO

Consumption of omega-3 (n-3) polyunsaturated fatty acids (PUFA) is related to improvement in the inflammatory response associated with decreases in metabolic disorders of obesity, such as low-grade inflammation and hepatic steatosis. Linseed (Linum usitatissimum) oil is a primary source of n-3 fatty acids (FAs) of plant origin, particularly α-linolenic acid, and provides an alternative for the ingestion of n-3 PUFA by persons allergic to, or wishing to avoid, animal sources. In our study, we evaluated the effect of the consumption of different lipidic sources on metabolic and inflammatory parameters in Wistar rats. We split 56 male rats into four groups that were fed for 60 days with the following diets: sesame oil, (SO, Sesamum indicum), linseed oil (LO), SO + LO (SLO), and a control group (CG) fed with animal fat. Our results reveal that the use of LO or SLO produced improvements in the hepatic tissue, such as lower values of aspartate aminotransferase, liver weight, and hepatic steatosis. LO and SLO reduced the weight of visceral fats, weight gain, and mediated the inflammation through a decrease in interleukin (IL)-6 and increase in IL-10. Though we did not detect any significant differences in the intestine histology and the purinergic system enzymes, the consumption of α-linolenic acid appears to contribute to the inflammatory and hepatic modulation of animals compared with a diet rich in saturated FAs and or unbalanced in n-6/n-3 PUFAs, inferring possible use in treatment of metabolic disorders associated with obesity and cardiovascular diseases.


Assuntos
Interleucina-10/metabolismo , Interleucina-6/metabolismo , Hepatopatia Gordurosa não Alcoólica/prevenção & controle , Ácido alfa-Linolênico/farmacologia , Tecido Adiposo , Animais , Ingestão de Alimentos , Regulação da Expressão Gênica/efeitos dos fármacos , Interleucina-10/genética , Interleucina-6/genética , Óleo de Semente do Linho/administração & dosagem , Óleo de Semente do Linho/química , Masculino , Valor Nutritivo , Distribuição Aleatória , Ratos , Ratos Wistar , Óleo de Gergelim/administração & dosagem , Óleo de Gergelim/química
2.
Cell Biochem Funct ; 35(7): 358-363, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28871607

RESUMO

This study aimed to characterize the activity of ectonucleoside triphosphate diphosphohydrolase (E-NTPDase; EC 3.6.1.5) in peritoneal cavity cells from BALB/c mice. E-NTPDase was activated in the presence of both calcium (1.5mM) and magnesium (1.5mM) ions. However, the activity was higher in the presence of Ca2+ . A pH of 8.5 and temperature of 37°C were the optimum conditions for catalysis. The apparent Km values were 0.51mM and 0.66mM for the hydrolysis of adenosine triphosphate (ATP) and adenosine diphosphate (ADP), respectively. The Vmax values were 136.4 and 120.8 nmol Pi/min/mg of protein for ATPase and ADPase activity, respectively. Nucleotide hydrolysis was inhibited in the presence of sodium azide (20mM, ATP: P < .05; ADP: P < .001), sodium fluoride (20mM; ATP and ADP: P < .001), and suramin (0.3mM; ATP: P < .01; ADP: P < .05), which is a known profile for NTPDase inhibition. Although all of the diphosphate and triphosphate nucleotides that were tested were hydrolyzed, enzyme activity was increased when adenine nucleotides were used as substrates. Finally, we stress that knowledge of the E-NTPDase catalytic biochemical properties in mouse peritoneal cavity cells is indispensable for properly determining its activity, as well as to fully understand the immune response profile in both healthy and sick cells.


Assuntos
Adenosina Trifosfatases/metabolismo , Linfócitos/enzimologia , Macrófagos/enzimologia , Neutrófilos/enzimologia , Cavidade Peritoneal/citologia , Animais , Cálcio/química , Cátions/química , Sobrevivência Celular , Células Cultivadas , Feminino , Concentração de Íons de Hidrogênio , Cinética , Linfócitos/citologia , Macrófagos/citologia , Magnésio/química , Camundongos , Camundongos Endogâmicos BALB C , Neutrófilos/citologia , Especificidade por Substrato , Temperatura
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