Publication:
Melatonin prevents neutrophil-mediated oxidative injury in Escherichia coli-induced pyelonephritis in rats

dc.contributor.authorsSener, Goksel; Tugtepe, Halil; Velioglu-Ogunc, Ayliz; Cetinel, Sule; Gedik, Nursal; Yegen, Berrak C.
dc.date.accessioned2022-03-12T17:19:41Z
dc.date.accessioned2026-01-11T16:19:40Z
dc.date.available2022-03-12T17:19:41Z
dc.date.issued2006
dc.description.abstractRegarding the mechanisms of renal scarring in pyelonephritis, several hypotheses have been put forward, among which oxidative stress is prominent. The present study investigated the possible protective effect of melatonin treatment against Escherichia coli- induced oxidative injury and scarring in renal tissue. For this purpose, 0.1 mL E. coli (ATCC 25922; 10 10 colony-forming units/mL) or saline was injected directly into the renal parenchyma of Wistar rats. Pyelonephritic rats were treated with either saline or melatonin (10 mg/ kg) intraperitoneally. Twenty-four hours or 1 wk after E. Coli injection, rats were decapitated and trunk blood samples were collected for BUN, creatinine, tumor necrosis factor- alpha (TNF-alpha) and lactate dehydrogenase (LDH) determination. In kidney samples, histological analysis was performed, and malondialdehyde (MDA), glutathione (GSH) levels, myeloperoxidase (MPO) activity and collagen contents were measured. Formation of reactive oxygen species was monitored using a chemiluminescence (CL) technique. Escherichia Coli inoculation caused a significant reduction in renal GSH levels, which was accompanied by significant increases in MDA levels, MPO activity, CL levels and collagen content of the renal tissues (P < 0.05-0.001). Similarly, serum TNF-a and, LDH, BUN and creatinine levels were elevated in the pyelonephritic rats when compared with control animals. Melatonin treatment reversed all these biochemical indices, as well as histopathological alterations induced by acute pyelonephritis. The protective effects of melatonin can be ascribed to its ability to inhibit neutrophil infilltration, to balance the oxidant-antioxidant status, and to regulate the generation of in. ammatory mediators, suggesting a future role for melatonin in the treatment of acute pyelonephritis.
dc.identifier.doi10.1111/j.1600-079X.2006.00357.x
dc.identifier.eissn1600-079X
dc.identifier.issn0742-3098
dc.identifier.pubmed16948782
dc.identifier.urihttps://hdl.handle.net/11424/228142
dc.identifier.wosWOS:000240292100004
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofJOURNAL OF PINEAL RESEARCH
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectantioxidants
dc.subjectEscherichia coli
dc.subjectglutathione
dc.subjectlipid peroxidation
dc.subjectmelatonin
dc.subjectmyeloperoxidase
dc.subjectpyelonephritis
dc.subjecttumor necrosis factor-alpha
dc.subjectMICROSOMAL MEMBRANE-FLUIDITY
dc.subjectREACTIVE OXYGEN
dc.subjectMYELOPEROXIDASE
dc.subjectSUPPRESSION
dc.subjectMECHANISMS
dc.subjectVITAMINS
dc.subjectOXIDANT
dc.subjectDAMAGE
dc.subjectMODEL
dc.titleMelatonin prevents neutrophil-mediated oxidative injury in Escherichia coli-induced pyelonephritis in rats
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage227
oaire.citation.issue3
oaire.citation.startPage220
oaire.citation.titleJOURNAL OF PINEAL RESEARCH
oaire.citation.volume41

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