🧫
AhR agonist effects on NEP in APP/PS1 mice
active
experiment
Created: 2026-04-10T14:45:43
By: etl-v1-backfill
Quality:
50%
✓ SciDEX
ID: exp-a77ffcdb-36f6-4378-b8c7-cca9739ce8ca
🧫 Experiment Protocol
ValidationAlzheimer's diseaseNEPAPP/PS1 miceproposed
In vivo study using APP/PS1 transgenic mice to investigate the effects of AhR agonists on NEP expression and enzyme activity. The experiment tested the same AhR ligands used in the cell culture studies (L-Kynurenine, FICZ, diosmin, and indole-3-carbinol) in a well-established mouse model of Alzheimer's disease. This study aimed to validate the cellular findings in a more physiologically relevant system and determine if AhR activation could have therapeutic potential for Alzheimer's disease through enhanced Aβ clearance mechanisms.
PRIMARY OUTCOME
NEP expression and enzyme activity
EXPECTED OUTCOMES
1. The intervention targeting NEP shifts NEP expression and enzyme activity in the predicted direction relative to the matched control arm.
2. Secondary disease-relevant readouts in Alzheimer's disease remain directionally concordant with the primary endpoint rather than showing isolated single-assay effects.
3. The effect persists after adjustment for baseline covariates, batch effects, or repeated-measures structure used in the study design.
SUCCESS CRITERIA
- Prespecified primary endpoint (NEP expression and enzyme activity) improves versus control with p < 0.05 or an equivalent corrected threshold used by the study.
- The effect size is biologically meaningful and reproduced across technical/biological replicates or the validation subset.
- Safety, data quality, and missingness remain within protocol-defined bounds so the result is interpretable rather than driven by attrition or assay failure.
PROTOCOL
1. Establish APP/PS1 mice cohorts for Alzheimer's disease and predefine inclusion, exclusion, and quality-control criteria before intervention. 2. Apply the experimental manipulation described for NEP, alongside matched control or comparator arms, and document dose, exposure window, and sample timing in a locked protocol log. 3. Measure NEP expression and enzyme activity together with orthogonal secondary readouts such as molecular, imaging, behavioral, or safety endpoints that are appropriate to the title and study design. 4. Use blinded outcome assessment where feasible, prespecified statistical analysis, and replicate the core readout across biological replicates or an independent validation subset. 5. Interpret results against the baseline study rationale: In vivo study using APP/PS1 transgenic mice to investigate the effects of AhR agonists on NEP expression and enzyme activity. The experiment tested the same AhR ligands used in the cell culture studies (L-Kynurenine, FICZ, diosmin, and indole-3-carbinol) in a
LINKED HYPOTHESES
Source: PMID 34522212 ↗
🧫 Experiment Extras
PATHWAY
AhR signaling pathway
MARKET PRICE
$0.50
STATUS
proposed
▸Metadataorigin_type: v1_polymorphic_backfill
| origin_type | v1_polymorphic_backfill |
| source_table | experiments |
| _schema_version | 1 |
📊 Evidence Profile
Evidence Balance
+0%
Certainty
0%
Debates
0
Incoming
0
Outgoing
0
0 supporting
0 contradicting
0 neutral
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