The apelin-apela receptor APJ is necessary for formation and healing of ischemia reperfusion-induced gastric ulcer in rats

The apelinergic system widely expressed and regulates hormone-enzyme secretion, motility, and protective mechanisms of the stomach. This system consists of the apelin receptor (APJ) and two peptides known as apela and apelin. The IR-induced experimental gastric ulcer model is a well-known and common...

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Veröffentlicht in:Peptides (New York, N.Y. : 1980) N.Y. : 1980), 2023-08, Vol.166, p.171027-171027, Article 171027
Hauptverfasser: Gemici, Burcu, Birsen, İlknur, İzgüt-Uysal, V. Nimet
Format: Artikel
Sprache:eng
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Zusammenfassung:The apelinergic system widely expressed and regulates hormone-enzyme secretion, motility, and protective mechanisms of the stomach. This system consists of the apelin receptor (APJ) and two peptides known as apela and apelin. The IR-induced experimental gastric ulcer model is a well-known and commonly used one that induces hypoxia and causes the release of proinflammatory cytokines. Expressions of apelin and its receptor APJ are induced by hypoxia and inflammation in the gastrointestinal tract. Apelin has been shown to affect angiogenesis positively, considered the most critical component of the healing process. Although it is known that apelin and AJP expressions are induced by inflammatory stimuli and hypoxia, stimulate endothelial cell proliferation and have a role in regenerative angiogenesis, no information or has been found in the literature regarding the role of APJ in the formation and healing of gastric mucosal lesions induced by I/R. So, we conducted a study to clarify the role of APJ in formation and healing mechanisms of IR-induced gastric lesions. Male Wistar rats were divided into five groups; control, sham-operated, IR, APJ antagonist treated-IR group (F13A+IR), and the healing groups. F13A was intravenously given to the animals. Gastric lesion index, mucosal blood flow, PGE2, NOx, 4-HNE-MDA, HO activity, and protein expressions of VEGF and HO-1 were measured. F13A application before the IR increased the mucosal injury, F13A application following the ischemia delayed the mucosal healing during the reperfusion period. Consequently, blocking apelin receptors may worsen gastric injury due to the IR and delay mucosal healing. •Chronic diseases, shock, alcohol, trauma, and stress can cause damage to the gastric mucosa.•Various defense mechanisms protect the gastric mucosa against deleterious factors.•Mucosal blood flow is vital in gastric mucosal protection against injury and during healing.•The apelinergic system comprises the APJ receptor and two ligands, Apelin and Apela.•APJ regulates gastric mucosal blood flow and may contribute to healing by increasing blood flow after gastric mucosal injury.
ISSN:0196-9781
1873-5169
DOI:10.1016/j.peptides.2023.171027