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Specimen Atlas of Research Peptides81 plates · MIT
Side-by-side · Research reference

CortagenvsLiraglutide

Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.

AAnimal-MechanisticHUMAN-REVIEWED11/35 cited
BFDA-ApprovedFlagship14/45 cited
Cortagen
Bioregulatory Tetrapeptide · Khavinson-School
TetrapeptideStructure
↓ LPO productsAntioxidant effectKozina 2007
AnimalEvidence level
Injectable · Animal models
Liraglutide
Daily GLP-1 RA · FDA-Approved
SQ · Abdomen / thigh / arm · Once daily

01Mechanism of Action

Parameter
Cortagen
Liraglutide
Primary target
Cerebral cortex tissue — molecular targets under investigation
Pathway
Antioxidant pathway modulation — suppression of LPO cascade, reduction of protein oxidative modificationKozina 2007
GLP-1R agonism → ↑glucose-dependent insulin, ↓glucagon, ↓gastric emptying, ↓appetiteSAXENDA (liraglutide) injectio 2014Marso 2016
Downstream effect
Decreased lipid peroxidation products, reduced oxidative protein damage, altered gene expression in cardiac tissueKozina 2007Anisimov 2004
Glycemic improvement, modest body-weight reduction, cardiovascular event reduction in high-risk T2DMarso 2016
Feedback intact?
Glucose-dependent insulin release preserves physiological feedback
Origin
Synthetic tetrapeptide derived from amino acid analysis of natural brain cortex peptide preparation CortexinAnisimov 2004
Modified GLP-1(7-37) with Lys26 substitution (Arg34) and C-16 palmitoyl-glutamate acylation for albumin bindingSAXENDA (liraglutide) injectio 2014
Antibody development

02Dosage Protocols

Parameter
Cortagen
Liraglutide
Animal model dose (rat)
Injection protocol (dose not specified in abstracts)
Multiple injections over study period.
Avian model dose (chicken)
40-day injection courseKuznik 2008
Compared to epithalon in hypophysectomized and aged birds.
Human peripheral nerve study
Therapeutic course (protocol details not provided)
Posttraumatic recovery context — reference cited but not detailed.
Evidence basis
Animal mechanistic studies
FDA-approved · Phase 3 RCTs (LEADER, SCALE)Marso 2016SAXENDA (liraglutide) injectio 2014
Route
Injectable (inferred from animal protocols)
Standard dose (T2D, Victoza)
Standard dose (weight, Saxenda)
3.0 mg / day (after 5-week titration)SAXENDA (liraglutide) injectio 2014
Frequency
Once daily, same time each day
Titration schedule
0.6 → 1.2 → 1.8 → 2.4 → 3.0 mg over 5 weeks
Mitigates GI side effects.
Duration
Indefinite for chronic indication
Reconstitution
Pre-filled commercial pen (no reconstitution)
Timing
Any time of day; consistent

04Side Effects & Safety

Parameter
Cortagen
Liraglutide
Antioxidant suppression
Suppression of antioxidant activity noted alongside LPO reductionKozina 2007
Mechanism unclear — possible homeostatic adaptation.
Immune/hemostasis effects
No effect on immunity or hemostasis parameters in avian hypophysectomy model (unlike epithalon)Kuznik 2008
Epithalon reversed deficits; cortagen did not.
Human safety data
No adverse events reported in peripheral nerve recovery context
Limited detail in available abstracts.
GI symptoms
Nausea, vomiting, diarrhea (very common during titration)SAXENDA (liraglutide) injectio 2014
Pancreatitis risk
Rare; discontinue if suspected
Thyroid C-cell tumours
Boxed warning — contraindicated in MEN2 / MTC historySAXENDA (liraglutide) injectio 2014
Hypoglycemia
Low risk as monotherapy; elevated with sulfonylureas / insulin
Heart rate
Modest ↑ resting HR (~2-3 bpm)
Cardiovascular benefit
↓ MACE in high-risk T2D (LEADER trial)Marso 2016
Pregnancy / OB
Contraindicated
Absolute Contraindications
Cortagen
Liraglutide
  • ·MTC personal or family history; MEN2
  • ·Pregnancy / breastfeeding
  • ·Hypersensitivity to liraglutide
Relative Contraindications
Cortagen
Liraglutide
  • ·Severe gastroparesis
  • ·History of pancreatitis
  • ·Severe gastrointestinal disease

05Administration Protocol

Parameter
Cortagen
Liraglutide
1. Preparation
Reconstitute lyophilised peptide with bacteriostatic water per supplier protocol. Exact volumes depend on concentration supplied.
Commercial pre-filled pen, no reconstitution required.
2. Injection site
Subcutaneous injection typical for bioregulatory peptides — abdomen or thigh. Rotate sites.
SQ — abdomen, thigh, or upper arm. Rotate sites.
3. Timing
Animal protocols used repeated dosing over weeks. Human timing not established — evening administration common in Khavinson tradition.
Once daily, same time each day. Take with or without food.
4. Storage
Lyophilised: refrigerate or freeze per supplier. Reconstituted: refrigerate 2–8 °C, use within guideline window.
Refrigerate 2–8 °C unopened; room temp ≤30 °C up to 30 days after first use.
5. Needle
Pen-supplied 32G needle.