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dc.contributor.authorKarademir, M.
dc.contributor.authorSonmez, M. A.
dc.contributor.authorAkcilar, R.
dc.contributor.authorKocak, E.
dc.contributor.authorYay, A.
dc.contributor.authorEser, O.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:38:56Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:38:56Z
dc.date.issued2018
dc.identifier.issn0006-9248
dc.identifier.issn1336-0345
dc.identifier.urihttps://dx.doi.org/10.4149/BLL_2018_113
dc.identifier.urihttps://hdl.handle.net/20.500.12418/6441
dc.descriptionWOS: 000451638900005en_US
dc.descriptionPubMed ID: 30345771en_US
dc.description.abstractOBJECTIVE: This study aimed to investigate the therapeutic effect of ozone in combination with insulin on cranial and spinal neuropathy in rats with diabetes mellitus (DM). MATERIALS AND METHODS: Sixty adult male Sprague Dawley rats were randomly divided into the following six groups (n = 10): control (C), ozone (O), diabetic (D), ozone-treated diabetic (DO), insulin-treated diabetic (DI), and ozone, insulin-treated diabetic (DOI). DM was induced by a single intraperitoneal (ip) streptozotocin injection (60 mg/kg), followed by 3 IU (ip) insulin administration for 60 days. Next, 1.1 mg/kg (50 mu g/ml) ozone was administered to the O, DO, and DOI groups for 60 days. After inducing diabetes, the total oxidant status (TOS) and total antioxidant status (TAS) were measured; the oxidative stress index (OSI) was calculated. The brain and spinal cord tissues were obtained for histopathological evaluation. This cross sectional study was conducted in Dumlupinar University Laboratory Animals Research Center e.g 11.03.2015 - 15.05.2015. RESULTS: TAS was higher in the DO, DI, and DOI groups than in the D group. TOS and OSI were lower in the DO, DI, and DOI groups than in the D group. Little pathological alterations with degenerated axons and vascular congestion were observed in the DO, DI, and DOI groups compared with the D group. CONCLUSION: Ozone with insulin can stimulate the endogenous antioxidant defense mechanism in diabetic neuropathy, thereby preventing reactive oxygen species-induced damage and protecting against cranial and spinal neuropathies.en_US
dc.language.isoengen_US
dc.publisherCOMENIUS UNIVen_US
dc.relation.isversionof10.4149/BLL_2018_113en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectintraperitoneal ozone gasen_US
dc.subjectcranial and spinal neuropathyen_US
dc.subjectdiabetesen_US
dc.titleEvaluation of therapeutic potential of intraperitoneal ozone gas in combination with insulin above cranial and spinal neuropathy in rats with diabetes mellitusen_US
dc.typearticleen_US
dc.relation.journalBRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTYen_US
dc.contributor.department[Karademir, M. -- Sonmez, M. A. -- Akcilar, R. -- Kocak, E. -- Yay, A. -- Eser, O.] Cumhuriyet Univ, Dept Neurosurg, Sch Med, TR-58140 Sivas, Turkey -- [Sonmez, M. A. -- Eser, O.] Balikesir Univ, Dept Neurosurg, Sch Med, Balikesir, Turkey -- [Akcilar, R.] Dumlupinar Univ, Dept Physiol, Sch Med, Kutahya, Turkey -- [Kocak, E.] Dumlupinar Univ, Dept Biochem, Sch Med, Kutahya, Turkey -- [Yay, A.] Erciyes Univ, Dept Histol & Embryol, Sch Med, Kayseri, Turkeyen_US
dc.contributor.authorIDKocak, Fatma Emel -- 0000-0001-5549-3883; karademir, mustafa -- 0000-0002-0734-9040en_US
dc.identifier.volume119en_US
dc.identifier.issue10en_US
dc.identifier.endpage641en_US
dc.identifier.startpage636en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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