Strain differences in the development of hypertension and glomerular lesions induced by deoxycorticosterone acetate salt in mice

被引:110
作者
Hartner, A [1 ]
Cordasic, N [1 ]
Klanke, B [1 ]
Veelken, R [1 ]
Hilgers, KF [1 ]
机构
[1] Univ Erlangen Nurnberg, Dept Med 4, Erlangen, Germany
关键词
albuminuria; blood pressure; deoxycorticosterone acetate; glomerulosclerosis; hypertension; mouse strains;
D O I
10.1093/ndt/gfg299
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. The genetic background may exert important modifying effects on the course and severity of experimental kidney diseases in mice. We investigated its influence on the development of hypertension and renal injury following treatment with deoxycorticosterone acetate (DOCA) salt in several mouse strains. Methods. Four mouse strains were used for comparison: 129/Sv, C57BL/6 and F1 and F2 intercrosses of 129/Sv x C57BL/6. Male mice were uninephrectomized and DOCA hypertension was induced for 6 weeks. DOCA animals and controls received 1% NaCl for drinking. Renal damage was evaluated following measurements of blood pressure, urine albumin and renal matrix expansion. Results. DOCA-induced blood pressure increase, glomerulosclerosis, interstitial fibrosis and albuminuria were markedly higher in 129/Sv than in C57BL/6 mice. F1 and F2 intercrosses displayed intermediate blood pressure, glomerular and interstitial fibrosis comparable to C57BL/6 but albuminuria as high as 129/Sv mice. Conclusions. 129/Sv mice are more susceptible to the development of DOCA-induced high blood pressure and renal damage than C57BL/6 mice. Intercrosses of both strains show a complex and non-uniform segregation of the susceptibility to DOCA-salt hypertension and nephrosclerosis.
引用
收藏
页码:1999 / 2004
页数:6
相关论文
共 14 条
[1]   Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded rat [J].
Brown, DM ;
Provoost, AP ;
Daly, MJ ;
Lander, ES ;
Jacob, HJ .
NATURE GENETICS, 1996, 12 (01) :44-51
[2]   TISSUE AND GENE SPECIFICITY OF MOUSE RENIN EXPRESSION [J].
FIELD, LJ ;
MCGOWAN, RA ;
DICKINSON, DP ;
GROSS, KW .
HYPERTENSION, 1984, 6 (04) :597-603
[3]  
Hansen PB, 2002, J AM SOC NEPHROL, V13, p335A
[4]   The α8 integrin chain affords mechanical stability to the glomerular capillary tuft in hypertensive glomerular disease [J].
Hartner, A ;
Cordasic, N ;
Klanke, B ;
Müller, U ;
Sterzel, RB ;
Hilgers, KF .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (03) :861-867
[5]   BEHAVIORAL AND CARDIOVASCULAR EFFECTS OF DISRUPTING THE ANGIOTENSIN-II TYPE-2 RECEPTOR GENE IN MICE [J].
HEIN, L ;
BARSH, GS ;
PRATT, RE ;
DZAU, VJ ;
KOBILKA, BK .
NATURE, 1995, 377 (6551) :744-747
[6]   EFFECTS ON BLOOD-PRESSURE AND EXPLORATORY-BEHAVIOR OF MICE LACKING ANGIOTENSIN-II TYPE-2 RECEPTOR [J].
ICHIKI, T ;
LABOSKY, PA ;
SHIOTA, C ;
OKUYAMA, S ;
IMAGAWA, Y ;
FOGO, A ;
NIIMURA, F ;
ICHIKAWA, I ;
HOGAN, BLM ;
INAGAMI, T .
NATURE, 1995, 377 (6551) :748-750
[7]  
Nakao N, 1998, AM J PATHOL, V152, P1237
[8]  
OLIVERIO MI, 1997, J AM SOC NEPHROL, V8, pA406
[9]   Effects of angiotensin-converting enzyme inhibitor and angiotensin type 1 receptor antagonist in deoxycorticosterone acetate-salt hypertensive mice lacking Ren-2 gene [J].
Peng, HM ;
Carretero, OA ;
Alfie, ME ;
Masura, JA ;
Rhaleb, NE .
HYPERTENSION, 2001, 37 (03) :974-980
[10]   Pathophysiology of progressive nephropathies [J].
Remuzzi, G ;
Bertani, T .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (20) :1448-1456