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10.1681/ASN.2014100971 http://scihub22266oqcxt.onion/10.1681/ASN.2014100971 C4769186!4769186!26116358     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26116358&cmd=llinks): Failed to open stream: HTTP request failed! 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Regression of Renal Disease by Angiotensin II Antagonism Is Caused by Regeneration of Kidney Vasculature |pdf=|usr=}}{{26116358}} gab.com Text Regression of Renal Disease by Angiotensin II Antagonism Is Caused by Regeneration of Kidney Vasculature JO: J Am Soc Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=26116358 #FOAvip Chronic renal insufficiency inexorably progresses in patients, such as it does after partial renal ablation in rats. However, the progression of renal diseases can be delayed by angiotensin II blockers that stabilize renal function or increase GFR, even in advanced phases of the disease. Regression of glomerulosclerosis can be induced by angiotensin II antagonism, but the effect of these treatments on the entire vascular tree is unclear. Here, using microcomputed tomography and scanning electron microscopy, we compared the size and extension of kidney blood vessels in untreated Wistar rats with those in untreated and angiotensin II antagonist?treated Munich Wistar Frömter (MWF) rats that spontaneously develop kidney disease with age. The kidney vasculature underwent progressive rarefaction in untreated MWF rats, substantially affecting intermediate and small vessels. Microarray analysis showed increased Tgf-? and endothelin-1 gene expression with age. Notably, 10-week inhibition of the renin-angiotensin system regenerated kidney vasculature and normalized Tgf-? and endothelin-1 gene expression in aged MWF rats. These changes were associated with reduced apoptosis, increased endothelial cell proliferation, and restoration of Nrf2 expression, suggesting mechanisms by which angiotensin II antagonism mediates regeneration of capillary segments. These results have important implications in the clinical setting of chronic renal insufficiency. Twit Text FOAVip Regression of Renal Disease by Angiotensin II Antagonism Is Caused by Regeneration of Kidney Vasculature ????J Am Soc Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=26116358 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26116358 #FOAvip English Wikipedia <ref>{{Cite pmid|26116358}}</ref> Regression of Renal Disease by Angiotensin II Antagonism Is Caused by Regeneration of Kidney Vasculature #MMPMID26116358 Remuzzi A; Sangalli F; Macconi D; Tomasoni S; Cattaneo I; Rizzo P; Bonandrini B; Bresciani E; Longaretti L; Gagliardini E; Conti S; Benigni A; Remuzzi G J Am Soc Nephrol 2016[Mar]; 27 (3): 699-705 PMID26116358show ga Chronic renal insufficiency inexorably progresses in patients, such as it does after partial renal ablation in rats. However, the progression of renal diseases can be delayed by angiotensin II blockers that stabilize renal function or increase GFR, even in advanced phases of the disease. Regression of glomerulosclerosis can be induced by angiotensin II antagonism, but the effect of these treatments on the entire vascular tree is unclear. Here, using microcomputed tomography and scanning electron microscopy, we compared the size and extension of kidney blood vessels in untreated Wistar rats with those in untreated and angiotensin II antagonist?treated Munich Wistar Frömter (MWF) rats that spontaneously develop kidney disease with age. The kidney vasculature underwent progressive rarefaction in untreated MWF rats, substantially affecting intermediate and small vessels. Microarray analysis showed increased Tgf-? and endothelin-1 gene expression with age. Notably, 10-week inhibition of the renin-angiotensin system regenerated kidney vasculature and normalized Tgf-? and endothelin-1 gene expression in aged MWF rats. These changes were associated with reduced apoptosis, increased endothelial cell proliferation, and restoration of Nrf2 expression, suggesting mechanisms by which angiotensin II antagonism mediates regeneration of capillary segments. These results have important implications in the clinical setting of chronic renal insufficiency. äRegression of Renal Disease by Angiotensin II Antagonism Is Caused by (epmc).pdf DeepDyve Pubget Overpricing