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A novel approach for preventing esophageal stricture formation: olmesartan prevented apoptosis
Murat Dereli, Bartlomiej E Krazinski, Suleyman Ayvaz1
1Department of Pediatric Surgery, Trakya University Faculty of Medicine, Edirne, Turkey. suleyayvaz@yahoo.com.
Abstract:
Accidentally ingested corrosive substances can cause functional and structural damage to the esophageal tissue resulting in stricture formation. It has been reported that the administration of olmesartan (OLM) can have anti-inflammatory, antifibrotic and antiapoptotic effects on injured tissue. The aim of our study was to check if OLM could prevent formation of scars in the corrosive esophageal burn model. Fifty-one Wistar Albino rats were divided into six groups: Control, Sham, OLM, Sham + OLM, Burn, and Burn + OLM. Olmesartan (5 mg/kg) was given by gavage once per day for 21 consecutive days after injury. The morphology of the esophagus was assessed after Masson trichrome staining, and apoptosis was evaluated using the terminal deoxynucleotidyl transferased UTP nick end labeling (TUNEL) method. The serum nucleosomes (as an indicator of apoptosis), serum p53 protein, and esophageal tissue p53 protein levels of each group were measured by immunoassays. Muscularis mucosa damage, submucosal collagen deposition, and tunica muscularis injury in the Burn + OLM group decreased significantly compared with the Burn group (p < 0.05). Similarly, the number of apoptotic cells in the Burn + OLM group decreased compared with the Burn group (p < 0.05). Serum levels of nucleosomes and p53 and tissue of p53 protein did not differ between the groups. Exogenously administered OLM can effectively prevent the occurrence of esophageal strictures caused by corrosive esophageal burns.
Insights
Olmesartan effectively prevents esophageal strictures after corrosive burns by reducing tissue damage and apoptosis. This study demonstrates olmesartan
Area of Science:
- Gastroenterology
- Pharmacology
- Regenerative Medicine
Background:
- Corrosive ingestion causes esophageal damage and stricture formation.
- Olmesartan exhibits anti-inflammatory, antifibrotic, and antiapoptotic properties in injured tissues.
Purpose of the Study:
- To investigate the efficacy of olmesartan in preventing esophageal stricture formation in a corrosive esophageal burn model.
Main Methods:
- Fifty-one rats were divided into six groups, including control and olmesartan-treated burn groups.
- Esophageal morphology, apoptosis (TUNEL), serum nucleosomes, and p53 protein levels were assessed.
- Olmesartan (5 mg/kg) was administered daily for 21 days post-injury.
Main Results:
- Olmesartan significantly reduced muscularis mucosa damage, submucosal collagen deposition, and tunica muscularis injury in burned esophagi.
- A significant decrease in apoptotic cells was observed in the olmesartan-treated burn group.
- Serum nucleosome and p53 levels, as well as tissue p53 protein, showed no significant differences between groups.
Conclusions:
- Olmesartan administration effectively prevents esophageal strictures resulting from corrosive esophageal burns.
- The drug's protective effects are linked to reduced tissue damage and apoptosis.
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