Hormones
Evidence: strong_human
Testosterone cypionate is an esterified prodrug of testosterone that undergoes hydrolysis in vivo to release free testosterone. It binds the androgen receptor (AR), activating genomic pathways via AR nuclear translocation and transcription of anabolic genes including IGF-1, satellite cell proliferation, and nitrogen retention. Additionally, testosterone exerts non-genomic effects through membrane-associated AR signaling, modulating calcium influx and MAPK/ERK pathways. Aromatization to estradiol via CYP19A1 (aromatase) maintains bone density and lipid profiles.
Standard: Research indicates 100-200 mg administered via intramuscular or subcutaneous injection every 7-14 days for testosterone replacement therapy.
Maintenance: Research indicates 100-150 mg weekly (or 50-75 mg twice weekly for more stable serum levels) titrated to trough total testosterone of 500-900 ng/dL.
Administration: intramuscularsubcutaneous
Timing: Inject on a consistent schedule. Twice-weekly dosing (e.g., Monday/Thursday) reduces peak-trough fluctuations. Morning injection preferred for alignment with circadian testosterone rhythm.
Duration: Ongoing for TRT. If discontinuing, taper and implement PCT protocol. Testicular function suppression occurs within 2-4 weeks of initiation.
Testosterone cypionate has an 8-day half-life following IM injection. Required bloodwork monitoring: Total testosterone (trough), free testosterone, estradiol (sensitive assay), CBC with hematocrit (every 3-6 months — hold if hematocrit >54%), PSA (baseline + annual if >40), comprehensive metabolic panel, lipid panel. Therapeutic blood donation recommended if hematocrit exceeds 52%. The Endocrine Society 2018 guidelines recommend against TRT in men planning fertility without concomitant hCG. Medical supervision required.
FDA-approved pharmaceutical product (Depo-Testosterone). Available from compounding pharmacies (200 mg/mL in grape seed or cottonseed oil). Ensure USP-grade with prescription.
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