Effects of losartan, in monotherapy or in association with hydrochlorothiazide, in chronic nephropathy resulting from losartan treatment during lactation
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2011
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Resumo |
Fanelli C, Fernandes BH, Machado FG, Okabe C, Malheiros DM, Fujihara CK, Zatz R. Effects of losartan, in monotherapy or in association with hydrochlorothiazide, in chronic nephropathy resulting from losartan treatment during lactation. Am J Physiol Renal Physiol 301: F580-F587, 2011. First published June 8, 2011; doi:10.1152/ajprenal.00042.2011.-We recently standardized a model (L(Lact)) of severe chronic kidney disease based on impaired nephrogenesis by suppression of angiotensin II activity during lactation (Machado FG, Poppi EP, Fanelli C, Malheiros DM, Zatz R, Fujihara CK. Am J Physiol Renal Physiol 294: F1345-F1353, 2008). In this new study of the L(Lact) model, we sought to gain further insight into renal injury mechanisms associated with this model and to verify whether the renoprotection obtained with the association of the angiotensin II receptor blocker losartan (L) and hydrochlorothiazide (H), which arrested renal injury in the remnant kidney model, would provide similar renoprotection. Twenty Munich-Wistar dams, each nursing six pups, were divided into control, untreated, and L(Lact) groups, given losartan (L; 250 mg.kg(-1).day(-1)) until weaning. The male LLact offspring remained untreated until 7 mo of age, when renal functional and structural parameters were studied in 17 of them, used as pretreatment control (L(Lact)Pre), and followed no further. The remaining rats were then divided among groups L(Lact) + V, untreated; L(Lact) + L, given L (50 mg.kg(-1).day(-1)) now as a therapy; L(Lact) + H, given H (6 mg.kg(-1).day(-1)); and L(Lact) + LH, given L and H. All parameters were reassessed 3 mo later in these groups and in age-matched controls. At this time, L(Lact) rats exhibited hypertension, severe albuminuria, glomerular damage, marked interstitial expansion/inflammation, enhanced cell proliferation, myofibroblast infiltration, and creatinine retention. L monotherapy normalized albuminuria and prevented hypertension and the progression of renal injury, inflammation, and myofibroblast infiltration. In contrast to the remnant model, the LH combination promoted only slight additional renoprotection, perhaps because of a limited tendency to retain sodium in L(Lact) rats. State of Sao Paulo Foundation for Research Support (FAPESP)[05/56066-3] Brazilian Council of Scientific and Technologic Development (CNPq)[304039/2006-3] Brazilian Council of Scientific and Technologic Development (CNPq)[308638/2010-7] |
Identificador |
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, v.301, n.3, p.F580-F587, 2011 1931-857X http://producao.usp.br/handle/BDPI/23657 10.1152/ajprenal.00042.2011 |
Idioma(s) |
eng |
Publicador |
AMER PHYSIOLOGICAL SOC |
Relação |
American Journal of Physiology-renal Physiology |
Direitos |
restrictedAccess Copyright AMER PHYSIOLOGICAL SOC |
Palavras-Chave | #angiotensin II #AT(1) receptor #thiazides #chronic kidney disease #CHRONIC KIDNEY-DISEASE #RENAL-FUNCTION #INTERSTITIAL FIBROSIS #CHRONIC HYPOXIA #ANGIOTENSIN-II #BLOOD-PRESSURE #PROGRESSION #INJURY #MODEL #ENDOCYTOSIS #Physiology #Urology & Nephrology |
Tipo |
article original article publishedVersion |