Rodent models of diabetic kidney disease: human translatability and preclinical validity

被引:5
|
作者
Sembach, Frederikke E. [1 ,2 ]
Ostergaard, Mette, V [1 ]
Vrang, Niels [1 ]
Feldt-Rasmussen, Bo [2 ,3 ]
Fosgerau, Keld [1 ]
Jelsing, Jacob [1 ]
Fink, Lisbeth N. [1 ]
机构
[1] Gubra ApS, Horsholm Kongevej 11B, DK-2970 Horsholm, Denmark
[2] Univ Copenhagen, Dept Clin Med, Blegdamsvej 3B, DK-2200 Copenhagen, Denmark
[3] Univ Copenhagen, Rigshosp, Dept Nephrol, Blegsdamsvej 9, DK-2100 Copenhagen, Denmark
关键词
DIPEPTIDYL PEPTIDASE-4 INHIBITION; INDUCED PODOCYTE INJURY; FACTOR-KAPPA-B; RENAL INJURY; BARDOXOLONE METHYL; SGLT2; INHIBITOR; RECEPTOR BLOCKADE; OXIDATIVE STRESS; MOUSE MODEL; PROTECTIVE ROLES;
D O I
10.1016/j.drudis.2020.05.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diabetic kidney disease (DKD) is the leading cause of end-stage renal disease (ESRD). Except for SGLT2 inhibitors and GLP-1R agonists, there have been few changes in DKD treatment over the past 25 years, when multifactorial intervention was introduced in patients with type 2 diabetes mellitus (T2DM). The unmet clinical need is partly due to the lack of animal models that replicate clinical features of human DKD, which has raised concern about the utility of these models in preclinical drug discovery. In this review, we performed a comprehensive analysis of rodent models of DKD to compare treatment efficacy from preclinical testing with outcome from clinical trials. We also investigated whether rodent models are predictive for clinical outcomes of therapeutic agents in human DKD.
引用
收藏
页码:200 / 217
页数:18
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