Please use this identifier to cite or link to this item: 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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