HGH 191AA

BodybuildingAnti-Aging

Recombinant human growth hormone (somatotropin), identical to the 191-amino-acid protein naturally produced by the anterior pituitary gland. FDA-approved for growth hormone deficiency and several other conditions under multiple brand names (Norditropin, Genotropin, Humatrope). Widely used off-label in anti-aging medicine and bodybuilding for its effects on body composition, recovery, and tissue regeneration.

Half-Life

2-3 hours

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Typical Dosage

Clinical (GH deficiency): 0.2-0.6 mg subcutaneous once daily. Anti-aging: 1-2 IU subcutaneous once daily, typically before bed. Bodybuilding: 2-4 IU subcutaneous once daily (up to 6-8 IU in advanced protocols). All doses injected subcutaneously, preferably in the evening to coincide with natural GH pulse timing.

Administration

Subcutaneous or intramuscular injection (daily)

Mechanism of Action

Human Growth Hormone is a 191-amino-acid single-chain polypeptide secreted by somatotroph cells of the anterior pituitary gland. It exerts its effects through two distinct pathways: direct action via GH receptors and indirect action through insulin-like growth factor 1 (IGF-1). When HGH binds to the GH receptor (a type I cytokine receptor), it induces receptor dimerization and activates the JAK2/STAT5 signaling cascade, which directly stimulates gene transcription for protein synthesis, cell proliferation, and lipolysis.

The indirect pathway is equally important. GH receptor activation in hepatocytes stimulates the production and secretion of IGF-1, a 70-amino-acid peptide that circulates bound to IGF binding proteins (primarily IGFBP-3 and the acid-labile subunit). Circulating IGF-1 acts on virtually every tissue in the body — promoting amino acid uptake and protein synthesis in skeletal muscle, stimulating chondrocyte proliferation in growth plates, enhancing osteoblast activity for bone formation, and supporting neuronal survival and myelination.

GH also has profound effects on metabolism independent of IGF-1. It directly stimulates lipolysis in adipocytes by activating hormone-sensitive lipase, mobilizing stored fat as free fatty acids for energy. It antagonizes insulin action in peripheral tissues (hence the diabetogenic risk), shifting the body's fuel preference from glucose to fatty acids. In muscle, GH promotes nitrogen retention and positive protein balance. The pulsatile pattern of natural GH secretion — with the largest pulse during deep sleep — is important for its physiological effects, which is why exogenous GH protocols often try to mimic this pattern.

Regulatory Status

FDA approved for GH deficiency, Turner syndrome, and other specific conditions. Prescription required. Off-label use is common. Multiple pharmaceutical brands (Norditropin, Genotropin, Humatrope).

Risks & Safety

Common: joint pain, carpal tunnel syndrome, water retention and peripheral edema, headache, paresthesia. Serious: insulin resistance and impaired glucose tolerance, potential acceleration of existing tumor growth, acromegalic features with chronic supraphysiological dosing. Rare: intracranial hypertension (benign), gynecomastia, hypothyroidism. Contraindicated in active malignancy, diabetic retinopathy, and critical illness. FDA approved for specific indications.

Research Papers

No research papers indexed yet. Papers are fetched from PubMed weekly.

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