Combination

    Neuroprotective Peptide Research Protocol

    Research protocol for studying neuroprotective peptides including Semax, Selank, and NAD+, covering their mechanisms in neuronal survival and neuroplasticity, dosing parameters, and cognitive assessment frameworks for neuroprotection research.

    By Alpine Labs Editorial Team | 20 min read
    Published · Last reviewed · Last updated
    Reviewed by Alpine Labs Editorial Team
    20-25 minutes 7 steps Intermediate

    Materials Needed

    • Reconstituted Semax (intranasal preparation)
    • Reconstituted Selank (intranasal preparation)
    • NAD+ (reconstituted for subcutaneous injection)
    • Metered-dose nasal spray devices
    • Insulin syringes (for NAD+)
    • Alcohol swabs
    • Cognitive assessment tools (detailed in Step 2)
    • Research log

    Dosing Calculator

    Calculate the injection volume needed for your target dose.

    Result:

    Injection Volume

    0.100 mL

    Syringe Units (U-100)

    10.0 units

    Doses Per Vial

    20

    Concentration: 2500 mcg/mL (2.50 mg/mL)

    1

    Understand Neuroprotective Mechanisms

    Semax is a synthetic ACTH(4-10) analog that upregulates BDNF (brain-derived neurotrophic factor) and NGF (nerve growth factor) expression in the hippocampus and cortex, enhancing neuroplasticity and neuronal survival. It also modulates the immune response in neural tissue. Selank is a synthetic analog of the endogenous tetrapeptide tuftsin that provides anxiolytic effects via GABA-A receptor modulation while also enhancing BDNF expression — it provides neuroprotection partly through stress reduction. NAD+ (nicotinamide adenine dinucleotide) supports neuronal energy metabolism, activates sirtuins (SIRT1, SIRT3) for mitochondrial protection, and is a substrate for PARP-mediated DNA repair in neurons.

    Tips

    • Semax and Selank are complementary — Semax is primarily neurotrophic while Selank adds anxiolytic neuroprotection
    • NAD+ decline is a hallmark of aging that contributes to mitochondrial dysfunction in neurons
    2

    Establish Cognitive and Neurological Baseline

    Before beginning the protocol, establish baseline cognitive measurements. Recommended assessments: working memory (N-back task or digit span), processing speed (Trail Making Test Part A), executive function (Trail Making Test Part B), verbal fluency (category and phonemic fluency tasks), reaction time (simple and choice reaction time tests), and subjective cognitive assessment (questionnaire rating memory, focus, clarity, and mood). Free computerized versions of many of these tests are available through research platforms.

    Estimated time: 30-45 minutes

    Cognitive assessments are sensitive to sleep deprivation, caffeine, and stress — standardize these variables

    Tips

    • Complete cognitive testing at the same time of day for each assessment to control for circadian effects
    • Practice effects are significant — run the test battery twice at baseline and use the second session as your true baseline
    3

    Review Dosing and Delivery Routes

    Literature-based research doses: Semax at 200-600 mcg intranasally, 1-2 times daily (morning and early afternoon). Selank at 250-500 mcg intranasally, 1-3 times daily. NAD+ at 50-250 mg subcutaneously, 1-3 times per week (or daily at lower doses). Semax and Selank are administered intranasally following the Intranasal Administration Protocol. NAD+ is administered subcutaneously following the Subcutaneous Injection Technique Protocol.

    NAD+ subcutaneous injections can cause localized stinging/burning at the injection site — this is a known and expected reaction

    Tips

    • Intranasal delivery for Semax and Selank bypasses the blood-brain barrier via the olfactory and trigeminal nerve pathways
    • Subcutaneous NAD+ avoids the GI degradation that limits oral NAD+ precursor bioavailability
    4

    Establish Administration Schedule

    Create a daily schedule for the neuroprotective protocol. Morning: Semax 200-300 mcg intranasal + Selank 250 mcg intranasal (administer 5-10 minutes apart to allow each to absorb from the nasal mucosa). Early afternoon: optional second Semax dose (omit if administering NAD+ in the afternoon). NAD+: 2-3 times per week, preferably on non-consecutive days. Avoid administering stimulating compounds (Semax) in the evening as they may affect sleep onset.

    Estimated time: 5 minutes

    Do not administer Semax within 4-6 hours of planned sleep time

    Tips

    • Semax has mild stimulatory properties — morning administration aligns with its mechanism
    • Selank's anxiolytic effects complement morning administration, particularly for research on stress-related cognitive impairment
    5

    Administer Intranasal Peptides

    Follow the Intranasal Administration Protocol for Semax and Selank. Load each peptide into its own dedicated metered-dose nasal spray device — do not share devices between compounds. Clear nasal passages before administration. Administer Semax first, wait 5-10 minutes, then administer Selank. Split each dose equally between nostrils when possible.

    Estimated time: 10 minutes

    Do not use a single spray device for multiple peptides — this causes cross-contamination and inconsistent dosing

    Tips

    • Label each spray device clearly — confusion between Semax and Selank is a common handling error
    • Store nasal spray devices in the refrigerator between uses
    6

    Administer NAD+ Injection

    Follow the Subcutaneous Injection Technique Protocol for NAD+. The abdominal subcutaneous site is standard. NAD+ injections are known to cause a warm, stinging sensation at the injection site lasting 5-15 minutes — this is a normal reaction to the compound. Inject slowly over 30-60 seconds to minimize discomfort. Rotate injection sites.

    Estimated time: 5 minutes

    If injection site reactions persist beyond 30 minutes or include swelling/induration, reduce the dose and reassess

    Tips

    • Slower injection reduces the intensity of the stinging sensation
    • Some researchers split larger doses into two smaller injection sites to distribute the local reaction
    7

    Reassess Cognition and Compile Results

    Repeat the full cognitive assessment battery at weeks 4, 8, and at protocol completion (typically 12 weeks). Compare each metric against baseline values. Calculate percentage change for quantitative tests (reaction time, N-back accuracy) and absolute change for scaled assessments. Compile subjective daily/weekly observations from your research log. Note any confounding variables (sleep changes, stress, illness, dietary changes) that occurred during the study period.

    Estimated time: 30-45 minutes per assessment

    Tips

    • Neuroprotective effects may not manifest as acute cognitive enhancement — subtle changes in sustained performance, stress resilience, and mood stability are meaningful endpoints
    • Consider extending follow-up beyond the administration period to assess persistence of effects

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