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. 2023 Oct 26;4(10):1479–1493. doi: 10.34067/KID.0000000000000227

Table 3.

The experimental models of diabetic kidney disease

Disease Induction Methods Models(Refs.) Pathology Stage Simulating
T1DM Drug-induced STZ mice80 • Mild-to-moderate albuminuria.
• Mild glomerular and tubular damage.
• No hypertension, glomerulosclerosis, or interstitial fibrosis.
Early
STZ/eNOS−/− mice82 • Albuminuria.
• Glomerulosclerosis.
• Interstitial fibrosis.
Advanced
Spontaneous Akita mice86 • Hyperglycaemia.
• Mild hypertension, modest albuminuria.
• No glomerular or interstitial fibrosis.
Early
Ove26 mice87 • Progressive albuminuria.
• Glomerulosclerosis, interstitial fibrosis.
• Poor viability.
Advanced
T2DM Spontaneous Zucker diabetic fatty rat92 • Hyperlipidemia.
• Moderate hypertension and obesity.
• Progressive renal injury.
• High cost and slow progression to CKD.
Advanced
db/db mice140 • Glomerular and tubular hypertrophy.
• Modest albuminuria.
• Mesangial matrix expansion.
• No glomerular and interstitial fibrosis.
Early
db/db mice with UNX89,90 • Proteinuria and tubular atrophy.
• Interstitial fibrosis.
• Inflammation.
Advanced
db/db mice with eNOS−/−91 • Albuminuria.
• Arteriolar hyalinosis.
• Glomerulosclerosis, interstitial fibrosis.
Advanced
ob/ob mice141 • Podocyte loss, GBM thickening.
• Mesangial matrix expansion.
• No mesangiolysis, glomerular sclerosis.
Early to modest

Early stage: mild-to-moderate albuminuria, mild mesangial expansion, reduced nephrin expression. Advanced stage: moderate to macroalbuminuria, severe mesangial expansion and thickened glomerular basement membrane, podocyte loss, glomerular sclerosis, and tubulointerstitial fibrosis. T1DM, type 1 diabetes mellitus; STZ, streptozotocin; eNOS, endothelial nitric oxide synthase; T2DM, type 2 diabetes mellitus; db/db, leptin receptor deficient; UNX, uninephrectomy; GBM, glomerular basement membrane; ob/ob, leptin deficient.