NAD+ Boosting and SIRT1 Activation to Reverse Cellular Senescence in Neurons

In-Vitro Score: 0.850 Price: $0.50 Alzheimer disease Primary cortical neurons from aged (18-month) mice or SAMP8 Status: proposed

What This Experiment Tests

In-Vitro experiment designed to assess clinical efficacy targeting N/A in Primary cortical neurons from aged (18-month) mice or SAMP8. Primary outcome: NAD+/NADH ratio, SA-β-gal positivity, mitochondrial OCR

Description

Evaluate whether NAD+ precursor supplementation (NMN) activates SIRT1/PGC1α signaling, restores mitochondrial function, and reduces senescence markers in aged neurons and senescence-accelerated mouse model (SAMP8).

TARGET GENE
N/A
MODEL SYSTEM
Primary cortical neurons from aged (18-month) mice or SAMP8
ESTIMATED COST
$35,000
TIMELINE
8 months
PATHWAY
N/A
SOURCE
auto-generated
PRIMARY OUTCOME
NAD+/NADH ratio, SA-β-gal positivity, mitochondrial OCR

Scoring Dimensions

Info Gain 0.82 (25%) Feasibility 0.78 (20%) Hyp Coverage 0.88 (20%) Cost Effect. 0.75 (15%) Novelty 0.80 (10%) Ethical Safety 0.00 (10%) 0.850 composite

Protocol

in-vitro

Expected Outcomes

NMN treatment increases NAD+/NADH ratio >2-fold, elevates SIRT1 activity, reduces SA-β-gal positivity by >40%, and restores mitochondrial oxygen consumption rate (OCR).

Success Criteria

NAD+/NADH ratio (colorimetric assay), SA-β-gal assay, mitochondrial OCR (Seahawk); threshold: p < 0.05 vs. aged vehicle control.

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