GHRP-2 vs LL-37 (Cathelicidin)

Side-by-side comparison of mechanisms, dosing, interactions, and stacking potential.

GHRP-2LL-37 (Cathelicidin)
CategoryPeptidesPeptides
Standard DoseResearch indicates 100-300 mcg administered 1-3 times daily via subcutaneous injection.Research indicates 50-100 mcg daily via subcutaneous injection for immune support.
TimingOn empty stomach, bedtime administration preferred. Wait 2+ hours after last meal.Morning administration preferred for immune support. Topical application directly to wound sites.
Cycle Duration8-16 week cycles.4-8 week cycles. Short-term use preferred due to limited long-term safety data.
Evidence Levelmoderate_humananimal_plus_anecdotal
A

GHRP-2

Peptides

Mechanism

GHRP-2 (Growth Hormone Releasing Peptide-2) is a synthetic hexapeptide GHS-R1a agonist that is the most potent of the GHRP family for GH release. It stimulates pituitary GH secretion through the ghrelin receptor while also modulating hypothalamic GHRH and somatostatin pathways. GHRP-2 increases GH, cortisol, prolactin, and ACTH release, but with less appetite stimulation than GHRP-6. It also has demonstrated anxiolytic properties and sleep-promoting effects.

Standard Dosing

Research indicates 100-300 mcg administered 1-3 times daily via subcutaneous injection.

Timing

On empty stomach, bedtime administration preferred. Wait 2+ hours after last meal.

Cycle Duration

8-16 week cycles.

Side Effects

  • Water retention
  • Moderate hunger increase (less than GHRP-6)
  • Cortisol elevation
  • Prolactin elevation
  • Tingling
  • Vivid dreams

Contraindications

  • Active cancer
  • Cushing's syndrome
  • Hyperprolactinemia
  • Pregnancy and breastfeeding

Best Stacking Partners

CJC-1295 (no DAC)SermorelinBPC-157

Mechanism

LL-37 is a 37-residue amphipathic helical antimicrobial peptide, the only human cathelicidin, that kills bacteria by forming tetrameric channels that perforate cytoplasmic membranes. Beyond direct antimicrobial activity, it modulates innate immunity through formyl-peptide receptor 2 (FPR2), induces chemotaxis of neutrophils and monocytes, upregulates CXCR4 and IL-8, and neutralizes bacterial endotoxins (LPS). It also promotes wound healing through keratinocyte migration and angiogenesis.

Standard Dosing

Research indicates 50-100 mcg daily via subcutaneous injection for immune support.

Timing

Morning administration preferred for immune support. Topical application directly to wound sites.

Cycle Duration

4-8 week cycles. Short-term use preferred due to limited long-term safety data.

Side Effects

  • Injection site pain and redness
  • Localized inflammation
  • Potential mast cell activation

Contraindications

  • Active autoimmune conditions (particularly lupus — LL-37 is implicated in SLE pathophysiology)
  • Pregnancy and breastfeeding
  • Psoriasis (may exacerbate)

Best Stacking Partners

KPVThymosin Alpha-1BPC-157

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