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CJC-1295 Downstream Effects: Pathway Comparison

IGF-1 Synthesis Hepatic GHR activation → IGF-1 gene transcription 72–96 hours post-dose 10–14 days Liver, then systemic distribution 1.6× baseline IGF-1 at 96h (JCEM study) Lipolysis Adipocyte HSL phosphorylation via GH receptor 6–12 hours post-dose 6–8 days (

This comparison does not assign a generated winner or score.

  • IGF-1 Synthesis
  • Hepatic GHR activation → IGF-1 gene transcription
  • 72–96 hours post-dose
  • 10–14 days
  • Liver, then systemic distribution
  • 1.6× baseline IGF-1 at 96h (JCEM study)
  • Lipolysis
  • Adipocyte HSL phosphorylation via GH receptor
  • 6–12 hours post-dose
  • 6–8 days (duration of GH elevation)
  • White adipose tissue (preferentially visceral)
  • 40–60% increase in FFA release (AJP study)
  • Protein Synthesis
  • mTOR pathway activation via IGF-1
  • 4–6 days post-dose
  • 7–10 days
  • Skeletal muscle myocytes
  • 30–50% increase in fractional synthesis rate (JAP study)
  • Mitochondrial Biogenesis
  • PGC-1α upregulation via GH and IGF-1
  • 5–7 days post-dose
  • 14–21 days
  • Skeletal muscle, hepatic tissue
  • 25–35% increase in mitochondrial density (Cell Metabolism study)
  • Professional Assessment
  • CJC-1295 downstream effects are temporally staggered. Measuring outcomes before day 5 captures GH release but misses the metabolic consequences that define the peptide's utility in body composition and recovery research.
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