Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/29668
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorBRAGANCA, Ana Carolina de-
dc.contributor.authorCANALE, Daniele-
dc.contributor.authorGONCALVES, Janaina Garcia-
dc.contributor.authorSHIMIZU, Maria Heloisa Massola-
dc.contributor.authorSEGURO, Antonio Carlos-
dc.contributor.authorVOLPINI, Rildo Aparecido-
dc.date.accessioned2018-11-21T17:09:23Z-
dc.date.available2018-11-21T17:09:23Z-
dc.date.issued2018-
dc.identifier.citationFRONTIERS IN MEDICINE, v.5, article ID 282, 15p, 2018-
dc.identifier.issn2296-858X-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/29668-
dc.description.abstractThe pathogenesis of chronic kidney disease (CKD) involves a very complex interaction between hemodynamic and inflammatory processes, leading to glomerular/vascular sclerosis, and fibrosis formation with subsequent evolution to end-stage of renal disease. Despite efforts to minimize the progression of CKD, its incidence and prevalence continue to increase. Besides cardiovascular diseases and infections, several studies demonstrate that vitamin D status could be considered as a non-traditional risk factor for the progression of CKD. Therefore, we investigated the effects of vitamin D deficiency (VDD) in the course of moderate CKD in 5/6 nephrectomized rats (Nx). Adult male Wistar rats underwent Sham surgery or Nx and were subdivided into the following four groups: Sham, receiving standard diet (Sham); Sham VDD, receiving vitamin D-free diet (VDD); Nx, receiving standard diet (Nx); and VDD+Nx, receiving vitamin D-free diet (VDD+Nx). Sham or Nx surgeries were performed 30 days after standard or vitamin D-free diets administration. After validation of vitamin D depletion, we considered only Nx and VDD+Nx groups for the following studies. Sixty days after surgeries, VDD+Nx rats exhibited hypertension, a greater decline in renal function and plasma FGF-23 levels, renal hypertrophy, as well as higher plasma levels of PTH and aldosterone. In addition, those animals presented more significant chronic tubulointerstitial changes (cortical interstitial expansion/inflammation/fibrosis), higher expression of collagen IV, fibronectin and alpha-smooth muscle actin, and lower expressions of JG12 and M2 macrophages. Also, VDD+Nx rats had greater infiltration of inflammatory cells (M1 macrophages and T-cells). Such changes were accompanied by higher expression of TGF-beta 1 and angiotensinogen and decreased expression of VDR and Klotho protein. Our observations indicate that vitamin D deficiency impairs the renal function and worsens the renovascular and morphological changes, aggravating the features of moderate CKD in 5/6 nephrectomized rats.-
dc.description.sponsorshipFundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2010/52294-0, 2015/05513-1]-
dc.language.isoeng-
dc.publisherFRONTIERS MEDIA SA-
dc.relation.ispartofFrontiers in Medicine-
dc.rightsopenAccess-
dc.subjectchronic kidney disease-
dc.subjectvitamin D deficiency-
dc.subjectfibrosis-
dc.subjectinflammation-
dc.subject5/6 nephrectomy-
dc.subjectexperimental model-
dc.subject.otherrenin-angiotensin system-
dc.subject.otherd-receptor-
dc.subject.other25-hydroxyvitamin d-
dc.subject.otherfibrosis-
dc.subject.othermetabolism-
dc.subject.othermacrophage-
dc.subject.otherinjury-
dc.subject.otherfgf23-
dc.subject.other1,25-dihydroxyvitamin-d-
dc.subject.otherpathophysiology-
dc.titleVitamin D Deficiency Aggravates the Renal Features of Moderate Chronic Kidney Disease in 5/6 Nephrectomized Rats-
dc.typearticle-
dc.rights.holderCopyright FRONTIERS MEDIA SA-
dc.identifier.doi10.3389/fmed.2018.00282-
dc.identifier.pmid30370270
dc.subject.wosMedicine, General & Internal-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.description.articlenumber282-
hcfmusp.description.volume5-
hcfmusp.origemWOS-
hcfmusp.origem.idWOS:000446909900001-
hcfmusp.origem.id2-s2.0-85062707175
hcfmusp.publisher.cityLAUSANNE-
hcfmusp.publisher.countrySWITZERLAND-
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dc.description.indexPubMed-
hcfmusp.citation.scopus11-
hcfmusp.scopus.lastupdate2022-06-16-
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