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Exogenous Ghrelin Accelerates the Healing of Acetic Acid-Induced Colitis in Rats. | LitMetric

AI Article Synopsis

  • Previous studies indicated that ghrelin can reduce inflammation in colitis caused by substances like trinitrobenzene sulfonic acid and dextran sodium sulfate.
  • In our research, we found that after inducing colitis in rats using acetic acid, ghrelin treatment sped up the healing of the colon and lowered levels of inflammatory markers like IL-1β and TNF-α.
  • Overall, our findings suggest that ghrelin has a strong anti-inflammatory and healing effect in colitis, indicating its potential as a universal treatment option regardless of the cause.

Article Abstract

Previous studies have shown that ghrelin reduces colonic inflammation induced by trinitrobenzene sulfonic acid and dextran sodium sulfate. In the present study we determined the effect of treatment with ghrelin on the course of acetic acid-induced colitis in rats. Rectal administration of 3% acetic acid solution led to induction of colitis in all animals. Damage of the colonic wall was accompanied by an increase in mucosal concentration of pro-inflammatory interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α), as well mucosal activity of myeloperoxidase. Moreover, induction of colitis led to a reduction in colonic blood flow and DNA synthesis. Administration of ghrelin after induction of colitis led to faster regeneration of the colonic wall and reduction in colonic levels of IL-1β, TNF-α, and myeloperoxidase. In addition, treatment with ghrelin improved mucosal DNA synthesis and blood flow. Our study disclosed that ghrelin exhibits a strong anti-inflammatory and healing effect in acetic acid-induced colitis. Our current observation in association with previous findings that ghrelin exhibits curative effect in trinitrobenzene sulfonic acid- and dextran sodium sulfate-induced colitis suggest that therapeutic effect of ghrelin in the colon is universal and independent of the primary cause of colitis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037734PMC
http://dx.doi.org/10.3390/ijms17091455DOI Listing

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