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PLoS One ; 13(8): e0201375, 2018.
Article in English | MEDLINE | ID: mdl-30133465

ABSTRACT

Genetic and sexual factors influence the prevalence and the pathogenesis of many inflammatory disorders. In this study their relevance on the peripheral and central inflammatory status induced by a peripheral injection of lipopolysaccharide (LPS) was evaluated. BALB/c and CD-1 male and female mice were intraperitoneally injected with LPS. Spleens and brains were collected 2 and 72 hours later to study the levels of IL-6, TNF-α and IL-1ß. Percentage of microglia and astrocytes was determined in the cortex and hippocampus. Locomotor activity was registered before and during the 72 hours after LPS-treatment. Two hours after LPS-injection, a peripheral increase of the three cytokines was found. In brains, LPS increased TNF-α only in males with higher levels in CD-1 than BALB/c. IL-1ß increased only in CD-1 males. IL-6 increased in both strains with lower levels in BALB/c females. Peripheral and central levels of cytokines decline 72 hrs after LPS-treatment whilst a significantly increase of Iba-1 expression was detected. A dramatic drop of the locomotor activity was observed immediately after LPS injection. Our results show that acute systemic administration of LPS leads to peripheral and central increase of pro-inflammatory cytokines and microglia activation, in a strain and sex dependent manner.


Subject(s)
Brain , Lipopolysaccharides/toxicity , Microglia , Monokines , Spleen , Systemic Inflammatory Response Syndrome , Animals , Brain/immunology , Brain/physiology , Female , Male , Mice , Mice, Inbred BALB C , Microglia/immunology , Microglia/pathology , Monokines/genetics , Monokines/immunology , Organ Specificity/genetics , Organ Specificity/immunology , Sex Characteristics , Species Specificity , Spleen/immunology , Spleen/pathology , Systemic Inflammatory Response Syndrome/chemically induced , Systemic Inflammatory Response Syndrome/genetics , Systemic Inflammatory Response Syndrome/immunology , Systemic Inflammatory Response Syndrome/pathology
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