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single50MG

AICAR

50MG Protocol

AICAR 50MG

Injection Freq.

Inject once daily

Cycle Sched.

Daily subcutaneous injections for 8–12 weeks (research protocols)

Reconstitution

3.0 mL BAC water

Endurance enhancement signals in animal studies (exercise-mimetic)
Increased glucose uptake, fatty-acid oxidation, and mitochondrial enzymes via AMPK
Improved insulin sensitivity signals in animal models
Investigational therapeutic potential signals for metabolic syndrome/diabetic neuropathy protection in animals
1

Reconstitution Requirements

  • 3.0 mL BAC water

Escalation steps: 3

Defined through week 8

StepWeek RangeDoseUnits
1Weeks 1–21,000 mcg (1 mg)6
2Weeks 3–42,000 mcg (2 mg)12
3Weeks 5–83,000 mcg (3 mg)18

Inject once daily

Daily subcutaneous injections for 8–12 weeks (research protocols)

AICAR is described as an AMPK agonist that chemically makes cells behave as if they are energy depleted, similar to signals produced by exercise or fasting. The protocol explains that after administration, AICAR enters cells (notably skeletal muscle) and is converted to ZMP (AICAR monophosphate), an AMP analog that directly activates AMPK. AMPK is presented as a master regulator of energy homeostasis; once activated, it increases glucose uptake and fatty-acid oxidation, promotes mitochondrial biogenesis, and shifts metabolism toward higher energy output and improved endurance capacity. The page highlights classic animal research in which sedentary mice given AICAR demonstrated substantial endurance increases without training, illustrating the ‘exercise mimetic’ concept. It also notes that human safety data exist mainly from IV acadesine studies (not routine use), with generally tolerable short-term effects at much higher per-kg doses than research SC protocols. However, the page emphasizes that AICAR remains experimental, is not FDA-approved for therapeutic use, and that long-term human risk/benefit is not established.
Mild injection-site reactions (redness/irritation)
Long-term human risks unknown
experimental compound with no confirmed clinical benefit
  • Use aseptic technique: wipe vial stopper with alcohol; use new sterile syringe/needle
  • Add diluent slowly down the vial wall to minimize foaming
  • Gently swirl/roll until fully dissolved (do not shake)
  • Label vial with reconstitution date and concentration; protect from light
  • Refrigerate after reconstitution (commonly 2–8 °C) unless protocol states otherwise
  • Avoid repeated freeze–thaw cycles
  • Bacteriostatic Water for Injection contains benzyl alcohol preservative (multi-dose); follow protocol for beyond-use (many peptide protocols use ~28 days after mixing)
  • Avoid benzyl-alcohol-containing diluents in neonates/infants (safety warning for benzyl alcohol)