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Specimen Atlas of Research Peptides81 plates · MIT
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47Plate 47Reviewed 2026-04-27

MGF

IGF-1 Splice Variant

also known as Mechano Growth Factor, IGF-1Ec, MGF peptide, E-domain peptide

Mechano Growth Factor (MGF) is the IGF-1Ec splice variant produced locally in skeletal muscle in response to mechanical loading or damage. Distinguished from systemic IGF-1 by a unique 49-amino-acid E-domain that activates satellite cells and drives muscle repair independently of mature IGF-1. The synthetic 24-amino-acid E-domain peptide recapitulates MGF bioactivity in vitro and in rodent models but lacks human clinical validation.

§ I

At a glance

Splice variant
IGF-1Ec
Synthetic E-domain
24-AA
Human evidence
Animal only
Route

SQ · Research context only

§ II

Mechanism

Edit ↗

Primary target — Satellite cells (Pax7+) in skeletal muscle [moore-2018].

Pathway — Mechanical stress → IGF-1Ec mRNA upregulation → Local E-domain peptide release → Satellite cell activation.

Downstream effect — Satellite cell proliferation, myoblast differentiation, muscle fiber repair.

Origin — Alternative splicing of IGF-1 gene (exons 4-6) produces IGF-1Ec precursor; E-domain cleaved post-translationally [armakolas-2016][vassilakos-2017].

§ III

Dosage

Protocols described in the cited literature; not medical advice.

Edit ↗
ParameterValue
Synthetic peptide24-amino-acid E-domain sequenceCorresponds to human IGF-1Ec exons 4-6 region.
Rodent cardiac model200 μg/kg via peptide-eluting microstructuresPost-MI injection; improved ejection fraction by 8 weeks.
Acute delivery (mouse MI)Single bolus within 12 hrs post-infarction [shioura-2014]Delayed decompensation; no human protocol established.
Human evidenceNone — no published clinical trialsAll dosing extrapolated from animal models.
Detection in dopingFull-length MGF detected via LC-MS in illicit products [thevis-2014]WADA-prohibited since 2005; no therapeutic indication.
Evidence basisAnimal models + in vitro only
§ III · b

Reconstitution

A pure mass-to-volume utility. Enter what you have in the vial; the atlas computes the volume per dose. No prescription information.

Inputs
mg
mL
mcg
The calculator does pure mass-to-volume math. It does not recommend a dose. Refer to MGF's cited literature for protocol specifics.
Volumetric outputFig. C — reconstitution math
Volume per dose
0.100mL
10.0 units on a U-100 insulin syringe
Concentration
2500
mcg per mL
Doses per vial
20
at this dose
§ V

Adverse events

Severities follow the FDA / CTCAE convention.

Edit ↗
Human safety datasevere
None — no clinical trials published
Theoretical IGF-1 axis risksevere
Chronic IGF-1Ec overexpression linked to cancer progression (prostate, colorectal, breast)
Tumor promotionsevere
IGF-1Ec overexpressed in osteosarcoma, colorectal polyps with dysplasia, endometrial cancer
Antibody developmentmoderate
Unknown — no longitudinal human exposure data
Local injection reactionmild
Presumed similar to other peptides (erythema, induration) — no direct evidence
Dysregulated expression with agemoderate
Older adults (70+ yrs) show blunted IGF-1Ec response post-exercise vs young [moore-2018]
Absolute contraindications
  • Active malignancy or history of IGF-1-sensitive cancers (prostate, colorectal, breast, osteosarcoma)
  • No established therapeutic use — investigational only
Relative contraindications
  • Family history of IGF-1-axis malignancies
  • Use outside research setting
§ VI

Administration

Edit ↗
  1. 01
    No validated protocol

    MGF (E-domain peptide) has no approved clinical protocol. All published data derive from animal models or in vitro experiments.

  2. 02
    Synthetic peptide form

    Commercially available MGF corresponds to the 24-amino-acid human E-domain (hEc). Rodent E-domain (Eb) is structurally distinct and not interchangeable.

  3. 03
    Animal delivery models

    Rodent studies used peptide-eluting polymeric microstructures (cardiac) or direct intramuscular injection. Routes and doses non-translatable to humans. [pea-2015][shioura-2014]

  4. 04
    WADA prohibition

    MGF peptides prohibited in sport since 2005. Detection via LC-MS established for full-length MGF products. [thevis-2014]

  5. 05
    Research context only

    Any human use falls outside approved medical practice and regulatory frameworks. No safety or efficacy data exist.

§ VII

Synergies

Edit ↗
Appendix

Sources

25%

of 55 rendered claims carry a resolvable citation.

  1. [armakolas-2016]
    Armakolas 2016The role of the IGF-1 Ec in myoskeletal system and osteosarcoma pathophysiology.
    journal, 2016
  2. [moore-2018]
    Moore 2018Blunted satellite cell response is associated with dysregulated IGF-1 expression after exercise with age.
    journal, 2018
  3. [papageorgiou-2016]
    Papageorgiou 2016The human Ec peptide: the active core of a progression growth factor with species-specific mode of action.
    journal, 2016
  4. [pea-2015]
    Peña 2015Localized delivery of mechano-growth factor E-domain peptide via polymeric microstructures improves cardiac function following myocardial infarction.
    journal, 2015
  5. [shioura-2014]
    Shioura 2014Administration of a Synthetic Peptide Derived from the E-domain Region of Mechano-Growth Factor Delays Decompensation Following Myocardial Infarction.
    journal, 2014
  6. [taghibeikzadehbadr-2020]
    Taghibeikzadehbadr 2020Effect of different muscle contraction mode on the expression of Myostatin, IGF-1, and PGC-1 alpha family members in human Vastus Lateralis muscle.
    journal, 2020
  7. [thevis-2014]
    Thevis 2014Mass spectrometric characterization of a biotechnologically produced full-length mechano growth factor (MGF) relevant for doping controls.
    journal, 2014
  8. [vassilakos-2017]
    Vassilakos 2017Identification of the IGF-1 processing product human Ec/rodent Eb peptide in various tissues: Evidence for its differential regulation after exercise-induced muscle damage in humans.
    journal, 2017
Plate composed 2026-04-27 · maturity human-reviewed · schema v1 · Contributors: peptidesdb-core · 41 fields uncited — open contributions