The hormone ghrelin prevents traumatic brain injury induced intestinal dysfunction

Intestinal barrier breakdown following traumatic brain injury (TBI) is characterized by increased intestinal permeability, leading to bacterial translocation, and inflammation. The hormone ghrelin may prevent intestinal injury and have anti-inflammatory properties. We hypothesized that exogenous ghr...

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Veröffentlicht in:Journal of neurotrauma 2010-12, Vol.27 (12), p.2255-2260
Hauptverfasser: Bansal, Vishal, Ryu, Seok Yong, Blow, Chelsea, Costantini, Todd, Loomis, William, Eliceiri, Brian, Baird, Andrew, Wolf, Paul, Coimbra, Raul
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Sprache:eng
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Zusammenfassung:Intestinal barrier breakdown following traumatic brain injury (TBI) is characterized by increased intestinal permeability, leading to bacterial translocation, and inflammation. The hormone ghrelin may prevent intestinal injury and have anti-inflammatory properties. We hypothesized that exogenous ghrelin prevents intestinal injury following TBI. A weight-drop model created severe TBI in three groups of anesthetized Balb/c mice. Group TBI: animals underwent TBI only; Group TBI/ghrelin: animals were given 10 μg of ghrelin intraperitoneally prior and 1 h following TBI; Group sham: no TBI or ghrelin injection. Intestinal permeability was measured 6 h following TBI by detecting serum levels of FITC-Dextran after injection into the intact ileum. The terminal ileum was harvested for histology, expression of the tight junction protein MLCK and inflammatory cytokine TNF-α. Permeability increased in the TBI group compared to the sham group (109.7 ± 21.8 μg/mL vs. 32.2 ± 10.1 μg/mL; p 
ISSN:0897-7151
1557-9042
DOI:10.1089/neu.2010.1372