Unilateral ureteral obstruction model for hyperoside treatment

Validation Score: 0.900 Price: $0.50 chronic kidney disease unilateral ureteral obstruction mice Status: proposed

What This Experiment Tests

Validation experiment designed to validate causal mechanisms targeting ACAT1 in unilateral ureteral obstruction mice. Primary outcome: reduction in renal fibrosis and mitochondrial injury

Description

A second mouse model using unilateral ureteral obstruction (UUO) was employed to validate the renoprotective effects of hyperoside. This model provides an alternative approach to study kidney fibrosis progression and the therapeutic potential of hyperoside. Similar to the folic acid model, assessments included mitochondrial function, lipid metabolic remodeling, and fibrotic progression using multiple analytical approaches including histology, biochemistry, and ultrastructural examination.

TARGET GENE
ACAT1
MODEL SYSTEM
unilateral ureteral obstruction mice
ESTIMATED COST
$0
TIMELINE
0 months
PATHWAY
fatty acid oxidation, ketone body metabolism, ACAT1-l-carnitine-SIRT3 axis
SOURCE
extracted_from_pmid_41903436
PRIMARY OUTCOME
reduction in renal fibrosis and mitochondrial injury

Scoring Dimensions

Info Gain 0.00 (25%) Feasibility 0.00 (20%) Hyp Coverage 0.00 (20%) Cost Effect. 0.00 (15%) Novelty 0.00 (10%) Ethical Safety 0.00 (10%) 0.900 composite

📖 Wiki Pages

Mitochondriaentity

Protocol

surgical unilateral ureteral obstruction, hyperoside treatment, histological evaluation, biochemical analyses, electron microscopy

Expected Outcomes

consistent renoprotective effects of hyperoside across different CKD models

Success Criteria

reproducible reduction in fibrotic progression and mitochondrial dysfunction

Related Hypotheses (1)

TREM2 R47H Metabolic Lock-in at Cholesterol Ester Accumulation0.672

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