Calcitriol reduces kidney development disorders in rats provoked by losartan administration during lactation

被引:13
作者
de Almeida, Lucas Ferreira [1 ]
Francescato, Heloisa Della Coletta [1 ]
Alves da Silva, Cleonice Giovanini [1 ]
Costa, Roberto Silva [2 ]
Coimbra, Terezila Machado [1 ]
机构
[1] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Physiol, Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Pathol, Ribeirao Preto, SP, Brazil
关键词
ANGIOTENSIN-II RECEPTOR; GROWTH-FACTOR EXPRESSION; VITAMIN-D; PARATHYROID-HORMONE; CELL-PROLIFERATION; RENAL-FUNCTION; NEPHROPATHY; INHIBITION; MECHANISMS; BLOCKADE;
D O I
10.1038/s41598-017-11815-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Calcitriol has important effects on cellular differentiation and proliferation, as well as on the regulation of the renin gene. Disturbances in renal development can be observed in rats exposed to angiotensin II (AngII) antagonists during lactation period. The lack of tubular differentiation in losartan-treated rats can affect calcitriol uptake. This study evaluated the effect of calcitriol administration in renal development disturbances in rats provoked by losartan (AngII type 1 receptor antagonist) administration during lactation. Animals exposed to losartan presented higher albuminuria, systolic blood pressure, increased sodium and potassium fractional excretion, and decreased glomerular filtration rate compared to controls. These animals also showed a decreased glomerular area and a higher interstitial relative area from the renal cortex, with increased expression of fibronectin, alpha-SM-actin, vimentin, and p-JNK; and an increased number of macrophages, p-p38, PCNA and decreased cubilin expression. Increased urinary excretion of MCP-1 and TGF-beta was also observed. All these alterations were less intense in the losartan + calcitriol group. The animals treated with calcitriol showed an improvement in cellular differentiation, and in renal function and structure. This effect was associated with reduction of cell proliferation and inflammation.
引用
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页数:11
相关论文
共 49 条
[1]   Antiproteinuric effect of oral paricalcitol in chronic kidney disease [J].
Agarwal, R ;
Acharya, M ;
Tian, J ;
Hippensteel, RL ;
Melnick, JZ ;
Qiu, P ;
Williams, L ;
Batlle, D .
KIDNEY INTERNATIONAL, 2005, 68 (06) :2823-2828
[2]   Histopathological and ultrastructural effects of Losartan on embryonic rat kidney [J].
Akil, I ;
Inan, S ;
Gurcu, B ;
Nazikoglu, A ;
Ozbilgin, K ;
Muftuoglu, S .
ACTA HISTOCHEMICA, 2005, 107 (04) :291-300
[3]   Glomerular developmental chronology in human fetuses [J].
Almeida, JR ;
Passos, MAF ;
Souza, ERM ;
Mandarim-de-Lacerda, CA .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2003, 7 (04) :492-493
[4]   Overload proteinuria is followed by salt-sensitive hypertension caused by renal infiltration of immune cells [J].
Alvarez, V ;
Quiroz, Y ;
Nava, M ;
Pons, H ;
Rodríguez-Iturbe, B .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2002, 283 (05) :F1132-F1141
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   The potential regulatory role of vitamin D in the bioenergetics of inflammation [J].
Calton, Emily K. ;
Keane, Kevin N. ;
Soares, Mario J. .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2015, 18 (04) :367-373
[7]  
Cha JH, 2001, J AM SOC NEPHROL, V12, P1410, DOI 10.1681/ASN.V1271410
[8]   Neonatal losartan treatment suppresses renal expression of molecules involved in cell-cell and cell-matrix interactions [J].
Chen, Y ;
Lasaitiene, D ;
Gabrielsson, BG ;
Carlsson, LMS ;
Billig, H ;
Carlsson, B ;
Marcussen, N ;
Sun, XF ;
Friberg, P .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (05) :1232-1243
[9]   MAPK and angiotensin II receptor in kidney of newborn rats from losartan-treated dams [J].
Coelho Balbi, Ana Paula ;
Santana Marin, Evelyn Cristina ;
Francescato, Heloisa Della Coletta ;
Costa, Roberto Silva ;
Coimbra, Terezila Machado .
PEDIATRIC NEPHROLOGY, 2008, 23 (09) :1433-1444
[10]   Early events leading to renal injury in obese Zucker (fatty) rats with type II diabetes [J].
Coimbra, TM ;
Janssen, U ;
Gröne, HJ ;
Ostendorf, T ;
Kunter, U ;
Schmidt, H ;
Brabant, G ;
Floege, J .
KIDNEY INTERNATIONAL, 2000, 57 (01) :167-182