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Endothelin-1 receptor A antagonist rescue in male CD2AP mice

active
experiment Created: 2026-04-06T12:34:46 By: etl-v1-backfill Quality: 50% ✓ SciDEX ID: exp-2b909d11-31b9-42fb-9fa7-9c4a95806d88
🧫 Experiment Protocol ValidationAlzheimer's diseaseCD2APmale miceproposed
Pharmacological intervention study testing whether blocking endothelin-1 receptor A signaling can rescue vascular impairments in CD2AP mutant mice, with sex-specific analysis. This therapeutic experiment administered endothelin-1 receptor A antagonists to mice with reduced endothelial CD2AP and assessed whether this treatment could restore normal cerebrovascular function. The study revealed male-specific rescue effects, suggesting sex-dependent mechanisms in CD2AP-related vascular dysfunction.
PRIMARY OUTCOME
partial rescue of vascular impairments in male mice only
EXPECTED OUTCOMES
1. The intervention targeting CD2AP shifts partial rescue of vascular impairments in male mice only 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 (partial rescue of vascular impairments in male mice only) 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 male mice cohorts for Alzheimer's disease and predefine inclusion, exclusion, and quality-control criteria before intervention. 2. Apply the experimental manipulation described for CD2AP, alongside matched control or comparator arms, and document dose, exposure window, and sample timing in a locked protocol log. 3. Measure partial rescue of vascular impairments in male mice only 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: Pharmacological intervention study testing whether blocking endothelin-1 receptor A signaling can rescue vascular impairments in CD2AP mutant mice, with sex-specific analysis. This therapeutic experiment administered endothelin-1 receptor A antagonists to mice
🧫 Experiment Extras
PATHWAY
endothelin-1 signaling, cerebrovascular function
MARKET PRICE
$0.50
STATUS
proposed
Metadataorigin_type: v1_polymorphic_backfill
origin_typev1_polymorphic_backfill
source_tableexperiments
_schema_version1
📊 Evidence Profile
Evidence Balance
+0%
Certainty
0%
Debates
0
Incoming
0
Outgoing
0
0 supporting 0 contradicting 0 neutral
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