Mice received a low-dose (5 mg/kg) initially for the first treatment to acclimate mice for long-term treatment, followed by monthly high-dose of psilocybin (15 mg/kg in sterile saline) or vehicle (sterile saline) via oral gavage (on conscious mice) once/month (10 treatments total)
According to the scaling factors in the table above, to convert a dose in mg/kg body weight to a human equivalent dose in mg/kg body weight, one needs to use a scaling factor of 12.3. This means that a dose of 12.3 mg/kg body weight for a mouse would be equivalent to a dose of 1 mg/kg body weight for a human being. In other words, a human needs 12.3-times lower dose on a body weight basis, to get the same effect as the mouse.
However, mice exhibit a significantly faster metabolic profile for psilocybin compared to humans, leading to a shorter half-life and more rapid systemic clearance of psilocin; the elimination half-life of psilocin is ~0.9 h in mice33 vs 1.8–3 h in humans34. Due to this rapid clearance in mice, a higher dose of 15 mg/kg was selected to ensure sufficient systemic exposure comparable to those observed in human clinical trials. It is also important to note that toxicology studies indicate that psilocybin is well tolerated in mice up to doses of 180–250 mg/kg35, which is well above the dose utilized in this study.
Using the above scaling factors, a 7.27 mg/kg body weight dose for a mouse would be equivalent to about 1 mg/kg body weight for a 70 kg adult human.
and putting new people's name on it that have not died. 