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https://hdl.handle.net/11499/9675
Title: | The effects of ozone therapy on caspase pathways, TNF-?, and HIF-1? in diabetic nephropathy | Authors: | Güçlü, A. Erken, H.A. Erken, G. Dodurga, Yavuz Yay, A. Özçoban, Ö. Şimşek, H. |
Keywords: | Caspase Diabetic nephropathy HIF-1? Ozone therapy TNF-? caspase 3 caspase 9 hypoxia inducible factor 1alpha insulin interleukin 1beta converting enzyme ozone streptozocin tumor necrosis factor alpha caspase Hif1a protein, rat messenger RNA photochemical smog tumor necrosis factor adult animal experiment animal model animal tissue Article controlled study diabetic nephropathy glomerulus histology kidney structure kidney tubule male nephritis nonhuman ozone therapy protein expression rat signal transduction animal apoptosis biosynthesis Diabetic Nephropathies experimental diabetes mellitus gene expression regulation genetics metabolism real time polymerase chain reaction Sprague Dawley rat therapeutic use TUNEL assay Animals Apoptosis Caspases Diabetes Mellitus, Experimental Gene Expression Regulation Hypoxia-Inducible Factor 1, alpha Subunit In Situ Nick-End Labeling Male Oxidants, Photochemical Ozone Rats Rats, Sprague-Dawley Real-Time Polymerase Chain Reaction RNA, Messenger Tumor Necrosis Factor-alpha |
Publisher: | Springer Netherlands | Abstract: | Background: Accelerated apoptosis plays a vital role in the development of diabetic vascular complications. Ozone may attenuate diabetic nephropathy by means of decreased apoptosis-related genes. The aim of our study was to investigate the effect of ozone therapy on streptozotocin-induced diabetic nephropathy in rats. Also the histopathological changes in diabetic kidney tissue with ozone treatment were evaluated. Methods: The rats were randomly divided into six groups (n = 7): control (C), ozone (O), diabetic (D), ozone-treated diabetic (DO), insulin-treated diabetic (DI), and ozone- and insulin-treated diabetic (DOI). D, DI, and DOI groups were induced by a single intraperitoneal injection of streptozotocin. Ozone was given to the O, DO, and DOI groups. Group DI and DOI received subcutaneous (SC) insulin (3 IU). All animals received daily treatment for 6 weeks. Results: Expressions of caspase-1-3-9, HIF-1?, and TNF-? genes were significantly higher in D group compared to C group (p < 0.05 for all). Ozone treatment resulted in significant decrease in the expressions of these genes in diabetic kidney tissue compared to both C and D group (p < 0.05 for all). Caspase-1-3-9, HIF-1?, and TNF-? gene expressions were found to be lower in DOI group compared to C group (p < 0.05 for all). Also adding ozone treatment to insulin therapy resulted in more significantly decrease in the expressions of these genes in diabetic tissue compared to only insulin-treated diabetic group (p < 0.05 for all). Regarding histological changes, ozone treatment resulted in decrease in the renal corpuscular inflammation and normal kidney morphology was observed. Both insulin and ozone therapies apparently improved kidney histological findings with less degenerated tubules and less inflammation of renal corpuscle compared to D, DO, and DI groups. Conclusion: Ozone therapy decreases the expressions of apoptotic genes in diabetic kidney tissue and improves the histopathological changes. © 2015, Springer Science+Business Media Dordrecht. | URI: | https://hdl.handle.net/11499/9675 https://doi.org/10.1007/s11255-015-1169-8 |
ISSN: | 0301-1623 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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