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MK-677 Side Effects Studies: Comparison Table

Elevated fasting glucose 60–70% (mean +0.3–0.5 mmol/L) GH-mediated hepatic gluconeogenesis + impaired peripheral glucose uptake Reverses 2–4 weeks post-discontinuation in short-term use; partial persistence in long-term use Low in metabolically healthy adults;

This comparison does not assign a generated winner or score.

  • Elevated fasting glucose
  • 60–70% (mean +0.3–0.5 mmol/L)
  • GH-mediated hepatic gluconeogenesis + impaired peripheral glucose uptake
  • Reverses 2–4 weeks post-discontinuation in short-term use; partial persistence in long-term use
  • Low in metabolically healthy adults; moderate-high in pre-diabetic or insulin-resistant individuals
  • Peripheral edema
  • 30–40% (mild lower-extremity swelling)
  • GH-induced renal sodium reabsorption via ENaC upregulation
  • Resolves spontaneously within 4–12 weeks as ANP/BNP compensate
  • Low—transient cosmetic concern, not indicative of organ dysfunction
  • Increased appetite
  • 50–65% (mean +200–400 kcal/day intake)
  • Ghrelin receptor (GHS-R1a) activation in hypothalamic arcuate nucleus
  • Reverses within 48–72 hours of discontinuation
  • Moderate—complicates caloric deficit protocols; neutral or beneficial in muscle-building contexts
  • Transient cortisol elevation
  • 40–50% (15–25% above baseline, peak 2–4h post-dose)
  • GH-stimulated ACTH release from anterior pituitary
  • Returns to baseline within 8–12 hours; no sustained hypercortisolemia
  • Low—peak elevations remain within physiological range
  • Mild prolactin increase
  • 30–40% (transient elevation 2–4h post-dose)
  • GH cross-activation of lactotroph receptors in pituitary
  • Returns to baseline within 8–12 hours; no chronic hyperprolactinemia
  • Low—no documented cases of gynecomastia or galactorrhea at standard doses
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