Unknown

Dataset Information

0

Beta-adrenergic receptor 1 selective antagonism inhibits norepinephrine-mediated TNF-alpha downregulation in experimental liver cirrhosis.


ABSTRACT:

Background

Bacterial translocation is a frequent event in cirrhosis leading to an increased inflammatory response. Splanchnic adrenergic system hyperactivation has been related with increased bacterial translocation. We aim at evaluating the interacting mechanism between hepatic norepinephrine and inflammation during liver damage in the presence of bacterial-DNA.

Animals and methods

Forty-six mice were included in a 16-week protocol of CCl(4)-induced cirrhosis. Laparotomies were performed at weeks 6, 10, 13 and 16. A second set of forty mice injected with a single intraperitoneal dose of CCl(4) was treated with saline, 6-hydroxidopamine, Nebivolol or Butoxamine. After 5 days, mice received E. coli-DNA intraperitoneally. Laparotomies were performed 24 hours later. Liver bacterial-DNA, norepinephrine, TNF-alpha, IL-6 and beta-adrenergic receptor levels were measured.

Results

Bacterial-DNA translocation was more frequent in CCl(4)-treated animals compared with controls, and increased as fibrosis progressed. Liver norepinephrine and pro-inflammatory cytokines were significantly higher in mice with vs without bacterial-DNA (319.7 ± 120.6 vs 120.7 ± 68.6 pg/g for norepinephrine, 38.4 ± 6.1 vs 29.7 ± 4.2 pg/g for TNF-alpha, 41.8 ± 7.4 vs 28.7 ± 4.3 pg/g for IL-6). Only beta-adrenergic receptor-1 was significantly increased in treated vs control animals (34.6 ± 7.3 vs 12.5 ± 5.3, p=0.01) and correlated with TNF-alpha, IL-6 and norepinephrine hepatic levels in animals with bacterial-DNA. In the second set of mice, cytokine levels were increased in 6-hydroxidopamine and Nebivolol (beta-adrenergic receptor-1 antagonist) treated mice compared with saline. Butoxamine (beta-adrenergic receptor-2 antagonist) didn't inhibit liver norepinephrine modulation of pro-inflammatory cytokines.

Conclusions

Beta-adrenergic receptor-1 mediates liver norepinephrine modulation of the pro-inflammatory response in CCl(4)-treated mice with bacterial-DNA.

SUBMITTER: Zapater P 

PROVIDER: S-EPMC3423372 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

altmetric image

Publications

Beta-adrenergic receptor 1 selective antagonism inhibits norepinephrine-mediated TNF-alpha downregulation in experimental liver cirrhosis.

Zapater Pedro P   Gómez-Hurtado Isabel I   Peiró Gloria G   González-Navajas José Manuel JM   García Irma I   Giménez Paula P   Moratalla Alba A   Such José J   Francés Rubén R  

PloS one 20120820 8


<h4>Background</h4>Bacterial translocation is a frequent event in cirrhosis leading to an increased inflammatory response. Splanchnic adrenergic system hyperactivation has been related with increased bacterial translocation. We aim at evaluating the interacting mechanism between hepatic norepinephrine and inflammation during liver damage in the presence of bacterial-DNA.<h4>Animals and methods</h4>Forty-six mice were included in a 16-week protocol of CCl(4)-induced cirrhosis. Laparotomies were p  ...[more]

Similar Datasets

| S-EPMC1572806 | biostudies-other
| S-EPMC7843213 | biostudies-literature
| S-EPMC2891313 | biostudies-literature
| S-EPMC6827910 | biostudies-literature
| S-EPMC5343290 | biostudies-literature
| S-EPMC5876717 | biostudies-literature
| S-EPMC8301320 | biostudies-literature
| S-EPMC2957335 | biostudies-literature
| S-EPMC3398957 | biostudies-literature
| S-EPMC4924748 | biostudies-literature