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Study breakdown

Ghrelin Protects the Stomach From Ischemia-Reperfusion Injury Through Prostaglandins

Animal StudyPreliminary evidence
The takeaway

Ghrelin protected against gastric ischemia-reperfusion injury through a prostaglandin/cyclooxygenase-dependent pathway, adding gastroprotection to ghrelin's growing list of GI effects.

Key finding

Ghrelin's gastroprotective effect against ischemia-reperfusion injury was mediated through the prostaglandin/COX pathway, with COX inhibitors (indomet

What the researchers found

Ghrelin's gastroprotective effect against ischemia-reperfusion injury was mediated through the prostaglandin/COX pathway, with COX inhibitors (indomethacin) blocking the protection — identifying the molecular mechanism for ghrelin's gastric mucosal defense.

Why it matters

Relevant for ghrp, gut-healing.

How the study worked

animal-study study on ghrp, gut-healing.

What this study cannot tell us

See abstract.

How to read the evidence

preliminary evidence.

When this study was published

Published in 2006.

The bigger picture

Advances peptide research.

Questions still open

  • Further research needed.
  • Clinical translation to evaluate.

Common questions

What was studied?
Ghrelin Protects the Stomach From Ischemia-Reperfusion Injury Through Prostaglandins
What was found?
Ghrelin protected against gastric ischemia-reperfusion injury through a prostaglandin/cyclooxygenase-dependent pathway, adding gastroprotection to ghrelin's growing list of GI effects.

Read the original research

Prostaglandin/cyclooxygenase pathway in ghrelin-induced gastroprotection against ischemia-reperfusion injury.

The Journal of pharmacology and experimental therapeutics, 319(1), 477-87

Citation

Brzozowski, Tomasz; Konturek, Peter C; Sliwowski, Zbigniew; Pajdo, Robert; Drozdowicz, Danuta; Kwiecien, Slawomir; Burnat, Grzegorz; Konturek, Stanislaw J; Pawlik, Wieslaw W. (2006). Prostaglandin/cyclooxygenase pathway in ghrelin-induced gastroprotection against ischemia-reperfusion injury.. The Journal of pharmacology and experimental therapeutics, 319(1), 477-87.