Characterization of susceptibility of inbred mouse strains to diabetic nephropathy

被引:233
作者
Qi, ZH
Fujita, H
Jin, JP
Davis, LS
Wang, YH
Fogo, AB
Breyer, MD
机构
[1] Vet Adm Med Ctr, Nashville, TN 37212 USA
[2] Vanderbilt Univ, Dept Med, Div Nephrol, Nashville, TN USA
[3] Vanderbilt Univ, Dept Pathol, Nashville, TN USA
[4] Vanderbilt Univ, Dept Physiol & Mol Biophys, Nashville, TN USA
关键词
D O I
10.2337/diabetes.54.9.2628
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Differential susceptibility to diabetic nephropathy has been observed in humans, but it has not been well defined in inbred strains of mice. The present studies characterized the severity of diabetic nephropathy in six inbred mouse strains including C57BL/6J, DBA/2J, FVB/NJ, MRL/MpJ, A/J, and KK/HIJ mice. Diabetes mellitus was induced using low-dose streptozotocin injection. Progression of renal injury was evaluated by serial measurements of urinary albumin excretion, glomerular filtration rate (GFR), and terminal assessment of renal morphology over 25 weeks. Despite comparable levels of hyperglycemia, urinary albumin excretion and renal histopathological changes were dramatically different among strains. DBA/2J and KK/HIJ mice developed significantly more albuminuria than C57BL/6J, MRL/MpJ, and A/J mice. Severe glomerular mesangial expansion, nodular glomerulosclerosis, and arteriolar hyalinosis were observed in diabetic DBA/2J and KK/HIJ mice. Glomerular hyperfiltration was observed in all diabetic strains studied except A/J. The significant decline in GFR was not evident over the 25-week period of study, but diabetic DBA/2J mice exhibited a tendency for GFR to decline. Taken together, these results indicate that differential susceptibility to diabetic nephropathy exists in inbred mice. DBA/2J and KK/HlJ mice are more prone to diabetic nephropathy, whereas the most widely used C57BL/6J mice are relatively resistant to development of diabetic nephropathy.
引用
收藏
页码:2628 / 2637
页数:10
相关论文
共 46 条
[31]   Genetic studies of late diabetic complications - The overlooked importance of diabetes duration before complication onset [J].
Rogus, JJ ;
Warram, JH ;
Krolewski, AS .
DIABETES, 2002, 51 (06) :1655-1662
[32]   Proteotoxicity in the endoplasmic reticulum: lessons from the Akita diabetic mouse [J].
Ron, D .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (04) :443-445
[33]   COMPLETE PROTECTION FROM LOW-DOSE STREPTOZOTOCIN-INDUCED DIABETES IN MICE [J].
ROSSINI, AA ;
WILLIAMS, RM ;
APPEL, MC ;
LIKE, AA .
NATURE, 1978, 276 (5684) :182-184
[34]   Diabetic kidney disease in the db/db mouse [J].
Sharma, K ;
McCue, P ;
Dunn, SR .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2003, 284 (06) :F1138-F1144
[35]   Mouse models of blood pressure regulation and hypertension [J].
Sugiyama F. ;
Yagami K.-I. ;
Paigen B. .
Current Hypertension Reports, 2001, 3 (1) :41-48
[36]   Concordance of murine quantitative trait loci for salt-induced hypertension with rat and human loci [J].
Sugiyama, F ;
Churchill, GA ;
Higgins, DC ;
Johns, C ;
Makaritsis, KP ;
Gavras, H ;
Paigen, B .
GENOMICS, 2001, 71 (01) :70-77
[37]   DIET-INDUCED TYPE-II DIABETES IN C57BL/6J MICE [J].
SURWIT, RS ;
KUHN, CM ;
COCHRANE, C ;
MCCUBBIN, JA ;
FEINGLOS, MN .
DIABETES, 1988, 37 (09) :1163-1167
[38]   Molecular profiling of diabetic mouse kidney reveals novel genes linked to glomerular disease [J].
Susztak, K ;
Böttinger, E ;
Novetsky, A ;
Liang, D ;
Zhu, YQ ;
Ciccone, E ;
Wu, DN ;
Dunn, S ;
McCue, P ;
Sharma, K .
DIABETES, 2004, 53 (03) :784-794
[39]   Genetic analysis of non-insulin-dependent diabetes mellitus in KK and KK-Ay mice [J].
Suto, J ;
Matsuura, S ;
Imamura, K ;
Yamanaka, H ;
Sekikawa, K .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1998, 139 (06) :654-661
[40]   COX-2 inhibition prevents insulin-dependent diabetes in low-dose streptozotocin-treated mice [J].
Tabatabaie, T ;
Waldon, AM ;
Jacob, JM ;
Floyd, RA ;
Kotake, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (02) :699-704