
IGF-1 LR3
The Muscle and Tissue Builder | Modified Growth Factor Analog
What is IGF-1 LR3?
IGF-1 LR3 is a synthetic 83-amino acid analog of human insulin-like growth factor-1 that has never been approved for human use in any country. Despite approximately 3x greater potency than native IGF-1 with a 20-30 hour half-life due to reduced IGF-binding protein interaction, no human clinical trials have ever been conducted.
The Muscle and Tissue Builder IGF-1 LR3 is a long-acting version of "Insulin-like Growth Factor," a hormone that is essential for cell growth and repair. It is unique because it causes hyperplasia, meaning it actually helps create new muscle cells rather than just making existing ones larger.
Key Benefits
Approximately 3x more potent than native IGF-1 with 20-30 hour half-life due to reduced IGFBP binding. Promotes both muscle hypertrophy and hyperplasia in animal models.
New Muscle Cells: Promotes the creation of new muscle fibers for long-term strength.
Rapid Recovery: Drastically cuts down time needed to heal from intense physical strain.
Nutrient Shunting: Forces nutrients like protein and carbs into muscle cells rather than fat cells.
Nerve Repair: Supports the health and regeneration of nerves and tissues.
Increased Endurance: Improves the capacity for long-duration physical activity.
Fat Oxidation: Helps the body stay lean while in a muscle-building phase.
Quick Start Guide
Typical Dose
20-40mcg for beginners
How Often
Once daily post-workout
Where to Inject
Subcutaneous: abdomen, thigh, or upper arm
Injection Timing
Within 15-30 minutes post-workout with immediate carbohydrate intake
Effects Timeline
Initial: 1-2 weeks. Notable: 2-4 weeks. Desensitization: 6 weeks.
Storage
Reconstituted: 2-8°C
Cycle Length
4-6 weeks maximum
Break Between
Equal or longer off-cycle (4-6+ weeks) for receptor recovery
Research Indications
🟢 Muscle Growth - Most Effective
Muscle Hypertrophy
Animal studies show 15-20% lean mass gains in 4 weeks through satellite cell activation and protein synthesis enhancement. No human data exists.
Anti-Catabolic Effects
Preserves lean mass in cachexia models through ubiquitin-proteasome inhibition. Cancer cachexia rats maintained 30% more muscle versus placebo.
Hyperplasia Induction
Unique ability to create new muscle fibers via satellite cell differentiation, not just enlarging existing fibers. Permanent structural changes possible.
🔵 Tissue Repair - Effective
Wound Healing Acceleration
Promotes keratinocyte migration, epithelialization, and collagen synthesis. Mouse studies show faster wound closure and reduced scarring.
Ligament/Tendon Recovery
Rat MCL injury model showed improved maximum force and stress with enhanced type-I collagen expression. May overcome mechanical unloading effects.
Burn Recovery
Children with severe burns treated with native IGF-1 showed protein-sparing effects. LR3 variant untested in humans but theoretically more potent.
⚪️ Metabolic - Moderate
Nutrient Partitioning
Directs calories toward muscle rather than fat storage. Inhibits glucose uptake in adipocytes while promoting muscle uptake.
Fat Loss Enhancement
Promotes lipolysis and fatty acid oxidation independent of caloric deficit. Particularly targets visceral adipose tissue in animal models.
Insulin Sensitivity (Acute)
Short-term use may improve glucose uptake, though chronic exposure causes paradoxical insulin resistance through receptor downregulation.
What to expect
Week 1-2: Increased pump, fullness, possible hypoglycemia episodes if carbs inadequate
Week 2-4: Enhanced recovery, strength gains, visible muscle fullness, possible water retention
Week 4-6: Maximum effects but approaching receptor desensitization. Joint stiffness common.
Post-cycle: Gradual loss of pumps over 1-2 weeks. Strength/size gains may persist if training maintained.
Side Effects & Safety
Side Effects | When to Stop |
|---|---|
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Mechanism of Action & Molecular Information
Full IGF-1 receptor agonist with reduced IGF-binding protein interaction. N-terminal extension and R3 substitution prevent sequestration, maintaining free circulating levels. Activates PI3K/Akt/mTOR and MAPK/ERK pathways.
Weight | Length | Type |
|---|---|---|
390.35 Da | 4 amino acids | Tetrapeptide |
Amino Acid Sequence: | ||
Ala-Glu-Asp-Gly | ||
References
Research Studies |
|---|
Rat Muscle Hypertrophy Study (Florini et al.)
Demonstrated 2.5x greater anabolic response compared to native IGF-1. Satellite cell activation and protein synthesis increased by 50% above baseline. Both hypertrophy and hyperplasia observed. |
Fetal Sheep Metabolic Study (Children's Hospital Colorado)
Acute infusion suppressed insulin secretion by 66%. Chronic infusion caused 4 animal deaths from hypoglycemia and hypoxemia. Significantly reduced circulating amino acids, particularly BCAAs. |
Pig Growth Inhibition Study
Contrary to expectations, decreased average daily gain and food intake. Reduced plasma IGFBP-3, IGF-1, and insulin. Growth hormone dropped 23% with 60% reduction in pulse area. |
Guinea Pig Organ Study
No significant body weight gain or feed intake changes. Increased fractional weights of adrenals, gut, kidneys, and spleen. Suggests organ-specific rather than systemic growth effects. |
Cancer Cachexia Rat Model
Low-dose IGF-1 preserved lean mass during cancer cachexia, reducing loss from -41.4g to -28.8g versus placebo. Demonstrates anti-catabolic properties even in disease states. |
Alzheimer's Mouse Model (5XFAD)
Improved body composition and reduced filamentous plaques in cortex. Increased inert plaques and reduced Aβ oligomers, but failed to improve cognitive symptoms. Highlights gap between cellular and functional outcomes. |
Important Note
This content is intended for educational purposes only and is not medical advice, diagnosis, or treatment.
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