This work has been retracted.
Effect of Adiponectin on Kidney Crystal Formation in Metabolic Syndrome Model Mice via Inhibition of Inflammation and Apoptosis
Year: 2013
Type: article
Abstract: The aims of the present study were to elucidate a possible mechanism of kidney crystal formation by using a metabolic syndrome (MetS) mouse model and to assess the effectiveness of adiponectin treatment for the prevention of kidney crystals. Further, we performed genome-wide expression analyses for investigating novel genetic environmental changes. Wild-type (+/+) mice showed no kidney crystal formation, whereas ob/ob mice showed crystal depositions in their renal tubules. However, this deposition was remarkably reduced by adiponectin. Expression analysis of genes associated with MetS-related kidney crystal formation identified 259 genes that were >2.0-fold up-regulated and 243 genes that were <0.5-fold down-regulated. Gene Ontology (GO) analyses revealed that the up-regulated genes belonged to the categories of immunoreaction, inflammation, and adhesion molecules and that the down-regulated genes belonged to the categories of oxidative stress and lipid metabolism. Expression analysis of adiponectin-induced genes related to crystal prevention revealed that the numbers of up- and down-regulated genes were 154 and 190, respectively. GO analyses indicated that the up-regulated genes belonged to the categories of cellular and mitochondrial repair, whereas the down-regulated genes belonged to the categories of immune and inflammatory reactions and apoptosis. The results of this study provide compelling evidence that the mechanism of kidney crystal formation in the MetS environment involves the progression of an inflammation and immunoresponse, including oxidative stress and adhesion reactions in renal tissues. This is the first report to prove the preventive effect of adiponectin treatment for kidney crystal formation by renoprotective activities and inhibition of inflammation and apoptosis.
Source: PLoS ONE
Institutions: Nagoya City University, Nagoya University
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,382
Awards: G1120741288, G1368990209, マクロファージの持つ結晶貪食作用による尿路結石防御機構の解明, G2205411738, Effect of impaired functional domains of osteopontin on renal crystal formation : Analyses of OPN transgenic and OPN knockout mice., Integrated elucidation of the urinary stone formation mechanism considered from heredity and environment factors, and development of the new therapeutic medicines, 新しい疾患関連遺伝子を用いた尿路結石の病態解明と予防への基礎研究, The elucidation of crystal formation mechanism through the renal tubular epithelial cell injury and mitochondria injury, The role of bladder microcirculation and Kit positive interstitial cells in OAB, The mechanism of urolithiasis formation and the analysis of adipocytokine under metabolic syndrome, G4989645906, Prevention of urolithiasis using anti-NF-kB drugs, G5446776535, G5998676740, G6330817147, G6915650811, Effects of functional domains of osteopontin on renal crystal formation, The role of macrophages for prevention of kidney stone formation, Biomolecular mechanism of urinary stone formation, and development of medicine, Anti-NF-kB reagents for prevention of urinary stone, Elucidation of the mechanism and involvement of mitochondrial collapes in the initial process of kidney stone formation, Cross sectional study from gene and environmental factor towards
OpenAlex ID: W2029378486
