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Ethanol intoxication alleviates the inflammatory response of remote organs to experimental traumatic brain injury
- Source :
- International Journal of Molecular Sciences, Volume 21, Issue 21, International Journal of Molecular Sciences, Vol 21, Iss 8181, p 8181 (2020), International journal of molecular sciences 21(21), 8181-(2020). doi:10.3390/ijms21218181
- Publication Year :
- 2020
- Publisher :
- Universität Ulm, 2020.
-
Abstract
- Traumatic brain injury (TBI) may cause damage to distant organs. Acute ethanol intoxication (EI) induces complex local and systemic anti-inflammatory effects and influences the early outcomes of traumatized patients. Here, we evaluated its effects on the BI-induced expression of local inflammatory mediators in the trauma-remote organs the lungs and liver. Male mice were exposed to ethanol as a single oral dose (5g&middot<br />kg&ndash<br />1, 32%) before inducing a moderate blunt TBI. Sham groups underwent the same procedures without TBI. Ether 3 or 6h after the TBI, the lung and liver were collected. The gene expression of HMGB1, IL-6, MMP9, IL-1&beta<br />and TNF as well as the homogenate protein levels of receptor for advanced glycation end products (RAGE), IL-6, IL-1&beta<br />and IL-10 were analyzed. Liver samples were immunohistologically stained for HMGB1. EI decreased the gene expressions of the proinflammatory markers HMGB1, IL-6, and MMP9 in the liver upon TBI. In line with the reduced gene expression, the TBI-induced protein expression of IL-6 in liver tissue homogenates was significantly reduced by EI at 3h after TBI. While the histological HMGB1 expression was enhanced by TBI, the RAGE protein expression in the liver tissue homogenates was diminished after TBI. EI reduced the histological HMGB1 expression and enhanced the hepatic RAGE protein expression at 6h post TBI. With regard to the lungs, EI significantly reduced the gene expressions of HMGB1, IL-6, IL-1&beta<br />and TNF upon TBI, without significantly affecting the protein expression levels of inflammatory markers (RAGE, IL-6, IL-1&beta<br />and IL-10). At the early stage of TBI-induced inflammation, the gene expression of inflammatory mediators in both the lungs and liver is susceptible to ethanol-induced remote effects. Taken together, EI may alleviate the TBI-induced pro-inflammatory response in the trauma-distant organs, the lungs and liver, via the HMGB1-RAGE axis.
- Subjects :
- Male
Interleukin-1beta
Receptor for Advanced Glycation End Products
physiopathology [Alcoholic Intoxication]
poisoning [Ethanol]
lcsh:Chemistry
pathology [Brain Injuries, Traumatic]
Mice
DDC 570 / Life sciences
Brain Injuries, Traumatic
TBI
HMGB1 Protein
lcsh:QH301-705.5
metabolism [Inflammation]
pathology [Lung]
Leber
Entzündung
Alkohol
pathology [Liver]
Interleukin-10
pharmacology [Ethanol]
drug effects [Liver]
immunology [Liver]
Liver
etiology [Inflammation]
ddc:540
Cytokines
Alcohol
metabolism [Lung]
Article
lung
metabolism [Interleukin-1beta]
ddc:570
metabolism [Receptor for Advanced Glycation End Products]
drug effects [Lung]
Animals
ddc:610
Cytokine
pharmacology [Central Nervous System Depressants]
pathology [Inflammation]
metabolism [Interleukin-10]
Inflammation
immunology [Lung]
complications [Brain Injuries, Traumatic]
Ethanol
metabolism [Cytokines]
metabolism [HMGB1 Protein]
Central Nervous System Depressants
metabolism [Brain Injuries, Traumatic]
nervous system diseases
Disease Models, Animal
prevention & control [Inflammation]
lcsh:Biology (General)
lcsh:QD1-999
IL1B protein, mouse
Lungs
Alcoholic Intoxication
DDC 610 / Medicine & health
metabolism [Liver]
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- International Journal of Molecular Sciences, Volume 21, Issue 21, International Journal of Molecular Sciences, Vol 21, Iss 8181, p 8181 (2020), International journal of molecular sciences 21(21), 8181-(2020). doi:10.3390/ijms21218181
- Accession number :
- edsair.doi.dedup.....aa63445878a4114a188f22ceebfbdcf8
- Full Text :
- https://doi.org/10.3390/ijms21218181