Is Benidipine Effective in Preventing Gastric Ischemia/Reperfusion Injury?

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Özet

Background and Objective: The preventive effect of benidipine on organs and tissues against oxidative and proinflammatory cytokine damage, whose production is elevated by I/R, has been demonstrated. The current study noted that benidipine affects the biochemical and histopathological effects of I/R therapy on gastric injury in rats. Materials and Methods: A total of 18 rats were divided into either a Sham operation group (SG), gastric ischemia/reperfusion (GIR) group or benidipine+gastric ischemia/reperfusion (BGIR) groups. Biochemical measures and histological exams were done in all three groups after I/R intervention. Results: The MDA, TNF-alpha, IL-1 beta and COX2 levels were significantly higher (p<0.001) in GIR compared to SG and BGIR, although tGSH and COX1 were significantly lower (p<0.001). The SG group was histopathologically normal. The surface epithelium broke off in spots, causing mild degeneration, the gland recesses were decreased, the gland neck areas were wide, the base areas were significantly oedematous and the blood capillaries showed moderate dilatation and congestion in the GIR group. Infiltration of polymorphonuclear cells was seen in the connective tissue surrounding the arteries and close to the gland bases. The BGIR group's histopathological results were not normal, although they were milder than the GIR group's. Conclusion: The results discovered that benidipine shifted the oxidant/antioxidant balance in I/R damage in favour of antioxidants, as well as the COX-1/COX-2 equilibrium in favour of COX-2, which is cytoprotective. It appears that administering benidipine for antioxidant and cytoprotective purposes before surgical operations that are likely to cause I/R damage may be advantageous.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/16675Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.3923/ijp.2022.1271.1277Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorBilici, Sami
dc.contributor.authorTas, Hakan Gokalp
dc.contributor.authorMamedov, Renad
dc.contributor.authorSuleyman, Bahadir
dc.contributor.authorKuyrukluyi, Ufuk
dc.contributor.authorYavuzer, Bulent
dc.contributor.authorBulut, Seval
dc.contributor.authorCoban, Abdulkadir
dc.contributor.authorSuleyman, Halis
dc.date.accessioned2026-10-18T20:36:32.825726593Z
dc.date.available2026-10-18T20:36:32.825726593Z
dc.date.issued2022
dc.description.abstractBackground and Objective: The preventive effect of benidipine on organs and tissues against oxidative and proinflammatory cytokine damage, whose production is elevated by I/R, has been demonstrated. The current study noted that benidipine affects the biochemical and histopathological effects of I/R therapy on gastric injury in rats. Materials and Methods: A total of 18 rats were divided into either a Sham operation group (SG), gastric ischemia/reperfusion (GIR) group or benidipine+gastric ischemia/reperfusion (BGIR) groups. Biochemical measures and histological exams were done in all three groups after I/R intervention. Results: The MDA, TNF-alpha, IL-1 beta and COX2 levels were significantly higher (p<0.001) in GIR compared to SG and BGIR, although tGSH and COX1 were significantly lower (p<0.001). The SG group was histopathologically normal. The surface epithelium broke off in spots, causing mild degeneration, the gland recesses were decreased, the gland neck areas were wide, the base areas were significantly oedematous and the blood capillaries showed moderate dilatation and congestion in the GIR group. Infiltration of polymorphonuclear cells was seen in the connective tissue surrounding the arteries and close to the gland bases. The BGIR group's histopathological results were not normal, although they were milder than the GIR group's. Conclusion: The results discovered that benidipine shifted the oxidant/antioxidant balance in I/R damage in favour of antioxidants, as well as the COX-1/COX-2 equilibrium in favour of COX-2, which is cytoprotective. It appears that administering benidipine for antioxidant and cytoprotective purposes before surgical operations that are likely to cause I/R damage may be advantageous.
dc.identifier.doi10.3923/ijp.2022.1271.1277
dc.identifier.eissn1812-5700
dc.identifier.endpage1277
dc.identifier.issn1811-7775
dc.identifier.issue6
dc.identifier.startpage1271
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/16675
dc.identifier.volume18
dc.identifier.wosWOS:000915725700018
dc.language.isoen
dc.publisherASIAN NETWORK SCIENTIFIC INFORMATION-ANSINET
dc.relation.ispartofINTERNATIONAL JOURNAL OF PHARMACOLOGY
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectOxidative stress
dc.subjectbenidipine
dc.subjectgastric tissue
dc.subjectischemia/reperfusion
dc.subjectreactive oxygen species
dc.subjectantioxidant
dc.subjectanti-inflammatory
dc.subjectISCHEMIA-REPERFUSION INJURY
dc.subjectEXPRESSION
dc.subjectRATS
dc.subjectPharmacology & Pharmacy
dc.titleIs Benidipine Effective in Preventing Gastric Ischemia/Reperfusion Injury?
dc.typeArticle
dspace.entity.typePublication
rdl.citation.wos0
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)