Publication:
Protective effect of chlorogenic acid on renal ischemia/reperfusion injury in rats

dc.contributor.authorŞEKERCİ, ÇAĞRI AKIN
dc.contributor.authorTANIDIR, YILÖREN
dc.contributor.authorsToprak, Tuncay; Sekerci, Cagri Akin; Aydin, Hasan Riza; Ramazanoglu, Mehmet Akif; Arslan, Fatma Demet; Basok, Banu Isbilen; Kucuk, Hatice; Kocakgol, Huseyin; Aksoy, Hamit Zafer; Asci, Seyhan Sumeyra; Tanidir, Yiloren
dc.date.accessioned2022-03-14T09:26:44Z
dc.date.accessioned2026-01-11T19:13:18Z
dc.date.available2022-03-14T09:26:44Z
dc.date.issued2020-06-24
dc.description.abstractObjectives: Ischemia/repetfusion (I/R) injury is a common cause of renal injury and to date, many pharmacological agents have been identified to decrease I/R injury. One of the potential compound that can target I/R injury is chlorogenic acid (CGA). It has potent anti-inflammatory, antibacterial, anti-oxidant, analgesic and antipyretic activities in in vitro experiments and in vivo (mama; models. The aim of the study was to investigate the protective characteristic of CGA on renal I/R injury. Material and Methods: 24 rats were randomly allocated to three groups (n = 8): Sham, I/R+CGA and I/R groups. CGA was administered intraperitoneally at a dose of 20 mg/kg, 10 min before reperfusion. I/R injury was achieved by clamping the left renal artery for 45 minutes, followed by reperfusion for 4 hours. The left kidneys of the rats were examined for tissue damage by histopathological and biochemical examination. For histological evaluation, EGTI scoring system was used. For biochemical examination total oxidant status, total antioxidant status and oxidative stress index were used. The power analysis indicated that 8 subjects per group would be required to produce 80% chance of achieving statistical significance at p < 0.05 level. The results are expressed as mean +/- SD. Mann-Whitney U was performed for statistical analysis. Results: Histopathological examination of the tissue damage revealed that all kidneys in the sham group were normal. I-R group had significantly higher histopathological scores than other groups. Histopathological improvement was seen after CGA treatment. TAS, TOS and OSI values of I-R group were significantly higher than sham group (0.88 vs 0.76 (p: 0.004), 13.8 vs 7.04 (p: 0.021) and 0.15 vs 0.09 (p: 0.034), respectively). In CGA treated group TAS, TOS and OSI levels were 0.84, 6.47 and 0.07, respectively. CGA treatment resulted in significant improvement in TOS and OSI parameters. Conclusions: CGA treatment provided marked improvement in renal histology and suppressed oxidative stress. Thus, CGA may have a protective effect in renal (issue against I/R injury.
dc.identifier.doi10.4081/aiua.2020.2.153
dc.identifier.eissn2282-4197
dc.identifier.issn1124-3562
dc.identifier.pubmed32597123
dc.identifier.urihttps://hdl.handle.net/11424/243128
dc.identifier.wosWOS:000612201300022
dc.language.isoeng
dc.publisherPAGEPRESS PUBL
dc.relation.ispartofARCHIVIO ITALIANO DI UROLOGIA E ANDROLOGIA
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectRenal ischemia
dc.subjectOxidative stress
dc.subjectChlorogenic acid
dc.subjectRat
dc.subjectISCHEMIA-REPERFUSION INJURY
dc.subjectIN-VITRO
dc.subjectANTIOXIDANT
dc.subjectEXTRACTS
dc.subjectDAMAGE
dc.titleProtective effect of chlorogenic acid on renal ischemia/reperfusion injury in rats
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage157
oaire.citation.issue2
oaire.citation.startPage153
oaire.citation.titleARCHIVIO ITALIANO DI UROLOGIA E ANDROLOGIA
oaire.citation.volume92

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