
From Peptidepedia, the trusted peptide wiki.


Mechano Growth Factor (MGF) is a splice variant of insulin-like growth factor-1 (IGF-1) that has garnered significant attention for its potential role in muscle repair, tissue regeneration, and satellite cell activation. Expressed locally in response to mechanical stress and muscle damage, MGF is believed to stimulate the proliferation of muscle stem cells (satellite cells) while delaying their differentiation—a unique property that distinguishes it from mature IGF-1. Popular among bodybuilders, athletes, and biohackers seeking accelerated recovery and enhanced muscle growth, MGF is typically administered via subcutaneous or intramuscular injection at doses ranging from 100–400 mcg per day, with protocols often spanning 4–6 weeks. The pegylated form (PEG-MGF) offers an extended half-life of 48–72 hours, allowing for less frequent dosing.
MGF, or Mechano Growth Factor, is a 24-amino acid peptide derived from the C-terminal E-domain of the IGF-1Ec splice variant (IGF-1Eb in rodents). It is produced endogenously when skeletal muscle experiences mechanical loading, stretch, or damage. Unlike the circulating IGF-1Ea isoform produced primarily in the liver, MGF acts locally in an autocrine/paracrine fashion at the site of tissue injury.
What makes MGF particularly interesting is its proposed mechanism of action. Research suggests that MGF activates quiescent satellite cells—the muscle stem cells responsible for repair and regeneration—prompting them to enter the cell cycle and proliferate. Importantly, MGF appears to promote proliferation while inhibiting premature differentiation, allowing for a larger pool of myogenic precursor cells before they fuse into mature muscle fibers.
Users and researchers have identified several potential benefits:
MGF is expressed as an early-phase response following muscle damage. When mechanical loading or microtears occur in muscle tissue, the IGF-1 gene undergoes alternative splicing to produce the MGF transcript. This pulse of MGF expression is believed to activate dormant satellite cells, causing them to exit quiescence and begin dividing.
Unlike mature IGF-1, which signals primarily through the IGF-1 receptor (IGF-1R), synthetic MGF peptide appears to work through an IGF-1R-independent mechanism. Studies have shown that MGF activates the ERK (extracellular signal-regulated kinase) pathway without activating the Akt pathway typically associated with IGF-1R signaling. This suggests MGF may have a distinct receptor or intracellular target that has yet to be fully characterized.
Research indicates a biphasic pattern of IGF-1 isoform expression during muscle repair. MGF (IGF-1Ec/Eb) levels rise rapidly within hours of injury and remain elevated during the proliferative phase. As MGF levels decline, IGF-1Ea expression increases, promoting differentiation and fusion of myoblasts into mature muscle fibers.
Beyond muscle, MGF has demonstrated neuroprotective effects. In brain ischemia models, the MGF E-peptide protected neurons from damage through mechanisms involving PKC activation, nuclear translocation of Nrf2, and increased heme oxygenase-1 expression—pathways associated with protection against oxidative stress-induced apoptosis.
For standard (non-pegylated) MGF, typical protocols involve:
The pegylated version has an extended half-life of 48–72 hours, allowing for less frequent administration:
Most users implement cycling protocols to prevent receptor desensitization:
MGF is administered via injection, with two primary methods:
Subcutaneous injection: The most common approach, typically into abdominal fat. This provides systemic distribution and is suitable for general recovery purposes.
Intramuscular injection: Some users inject directly into the target muscle group immediately after training. This localized approach is theorized to concentrate MGF's effects at the site of muscle damage, though evidence for superior efficacy is largely anecdotal.
Timing considerations:
Based on user reports and available research:
Weeks 1–2: Minimal visible changes; potential for improved recovery sensation and reduced delayed-onset muscle soreness (DOMS)
Weeks 3–4: Users often report enhanced recovery between training sessions, improved workout capacity, and early signs of improved muscle fullness
Weeks 5–8: More noticeable improvements in muscle density and recovery; some users report localized growth in targeted muscle groups when using intramuscular injection protocols
Long-term: Animal studies have shown a 25% increase in mean muscle fiber size after three weeks of intramuscular MGF injection in mice.
The scientific literature on MGF presents a nuanced picture. While preclinical studies have shown promising results, human clinical data remains limited.
Muscle research: Studies in rodents demonstrated that MGF expression correlates with satellite cell activation markers following muscle damage. The synthetic MGF-24aa-E peptide increased proliferation of desmin-positive myogenic precursor cells derived from both healthy and diseased muscles.
Bone healing: Research published in the Journal of Orthopaedic Research demonstrated that MGF-Ct24E peptide promoted osteoblast proliferation and accelerated bone-defect healing in rabbit models.
Cardiac protection: Intracoronary delivery of MGF peptide improved hemodynamic function and reduced cardiac damage following myocardial infarction in sheep models, with effects exceeding those of mature IGF-1.
Neuroprotection: The MGF E-peptide demonstrated strong neuroprotective effects in brain ischemia models, protecting neurons through mechanisms independent of the IGF-1 receptor.
Important caveat: A 2010 review in Endocrinology noted that definitive evidence for the existence of an endogenous 24-amino acid MGF peptide in vivo remains lacking, and the relationship between synthetic MGF peptide effects and endogenous IGF-1Ec expression requires further clarification.
MGF is commonly combined with other peptides and compounds:
With Growth Hormone Releasing Peptides (GHRPs): Combining MGF with GHRP-6 or GHRP-2 may enhance overall anabolic signaling by increasing endogenous growth hormone release.
With CJC-1295: This combination aims to create a synergistic effect on growth hormone and IGF-1 pathways.
With BPC-157: Some users combine MGF with BPC-157 for enhanced tissue repair, particularly for injury recovery.
With IGF-1 LR3: This combination is controversial; some suggest using them at different times of day to avoid receptor competition, while others avoid concurrent use entirely.
Timing considerations when stacking:
Reconstitution:
Storage:
Injection preparation:
MGF appears generally well-tolerated, but potential side effects include:
Common:
Less common:
Theoretical concerns:
Contraindications:
MGF is not approved by the U.S. Food and Drug Administration (FDA) for any medical use. The FDA has stated that it lacks important information regarding safety issues raised by PEG-MGF, including whether it would cause harm if administered to humans.
In the United States, MGF exists in a legal gray area:
International status varies by country, with some nations having stricter regulations on peptide sales and possession.
MGF is explicitly prohibited by the World Anti-Doping Agency (WADA). Peptide hormones categorized as mechano growth factors have been classified as prohibited substances under Section S2 (Peptide Hormones, Growth Factors, Related Substances, and Mimetics) of the WADA Prohibited List.
The prohibition applies:
Detection methods have advanced significantly, with WADA-accredited laboratories capable of detecting MGF and related peptides through mass spectrometry techniques. Athletes should be aware that MGF has been identified in black market products, confirming its availability and use in doping contexts.
MGF represents a fascinating area of peptide research with compelling preclinical evidence for muscle repair, satellite cell activation, and tissue regeneration. Its unique mechanism—promoting proliferation while delaying differentiation—distinguishes it from mature IGF-1 and suggests potential applications in recovery from injury, age-related muscle loss, and possibly neurodegenerative conditions.
However, users should approach MGF with appropriate caution. Human clinical trials are lacking, long-term safety data is limited, and the relationship between synthetic MGF peptide and endogenous IGF-1Ec expression remains incompletely understood. Quality control in the peptide market varies significantly, making source verification essential.
For those who choose to use MGF, starting with conservative doses, implementing proper cycling protocols, and monitoring for adverse effects represents a prudent approach. As with all research peptides, consultation with a knowledgeable healthcare provider is advisable.
What is the difference between MGF and PEG-MGF?
Standard MGF has a very short half-life of approximately 5–7 minutes in circulation. PEG-MGF has been modified through pegylation (attachment of polyethylene glycol), extending its half-life to 48–72 hours. This allows for less frequent dosing (2–3 times weekly versus daily) and potentially more sustained systemic effects.
Should I inject MGF into the muscle I trained?
Some users prefer intramuscular injection into the trained muscle group, theorizing this concentrates MGF's effects locally. However, subcutaneous injection provides systemic distribution and is simpler to perform. Scientific evidence definitively favoring one approach over the other in humans is lacking.
Can MGF be used for injury recovery?
Preclinical research suggests MGF may accelerate tissue repair, including muscle, bone, and potentially nerve tissue. Some users report improved recovery from injuries, though human clinical data is limited. MGF should not replace proper medical treatment for injuries.
How does MGF compare to IGF-1 LR3?
IGF-1 LR3 is a modified form of mature IGF-1 with extended half-life that works primarily through the IGF-1 receptor. MGF appears to work through different mechanisms, activating satellite cells and the ERK pathway independently of the IGF-1 receptor. Some users employ both at different times, though this approach lacks clinical validation.
Is MGF safe for long-term use?
Long-term safety data for MGF in humans is not available. Most protocols recommend cycling (4–6 weeks on, 2–4 weeks off) to prevent potential receptor desensitization and allow for assessment of effects. As with all growth factors, theoretical concerns exist regarding effects on cell proliferation.
Will MGF show up on a drug test?
Standard workplace drug tests do not screen for peptides like MGF. However, WADA-accredited laboratories can detect MGF, and it is prohibited in competitive sports. Athletes subject to anti-doping testing should not use MGF.
What is the best time to inject MGF?
Common protocols suggest post-workout injection (within 30 minutes of training) for localized effects, or pre-sleep injection to coincide with natural growth hormone release. Some users split doses between both times.
Can women use MGF?
MGF is not sex-specific in its mechanism of action, and women may theoretically use it for similar purposes as men. However, as with all research peptides, safety data specific to women is lacking, and pregnant or breastfeeding women should avoid use.
