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. 2013 May;41(5):975–986. doi: 10.1124/dmd.112.050724

TABLE 3.

Noncompartmental analysis of serum bufotenine PK in wild-type and Tg-CYP2D6 mice coadministered with harmaline and 5-MeO-DMT

Harmaline and 5-MeO-DMT were administered i.p. at 0 and 15 minutes, respectively.

Mice Parameters 5-MeO-DMT 2 mg/kg
5-MeO-DMT 10 mg/kg
Harmaline
0 mg/kg Harmaline
5 mg/kg Harmaline
15 mg/kg Harmaline
0 mg/kg Harmaline
5 mg/kg Harmaline
15 mg/kg
Wild-type Cmax (µM) 0.051 ± 0.009 0.132 ± 0.009* 0.075 ± 0.015*& 0.114 ± 0.023 0.185 ± 0.014* 0.131 ± 0.037*&
AUC (µM⋅min)a 2.69 ± 1.21 16.3 ± 1.4* 5.16 ± 0.76*& 5.66 ± 0.88 12.9 ± 1.2* 2.72 ± 0.34*&
Tg-CYP2D6 Cmax (µM) 0.053 ± 0.013 0.137 ± 0.014* 0.090 ± 0.010*& 0.151 ± 0.085 0.300 ± 0.030*# 0.170 ± 0.066*&
AUC (µM⋅min)a 1.82 ± 0.74 18.0 ± 1.5* 6.86 ± 1.33*& 7.30 ± 4.21 18.2 ± 1.9*# 3.59 ± 0.94*&
a

AUC15→105min for the treatments of 5 mg/kg harmaline plus 10 mg/kg 5-MeO-DMT, AUC15→45min for the treatments of 15 mg/kg harmaline plus 10 mg/kg 5-MeO-DMT, and AUC15 min→∞ for all other treatments.

*

P < 0.05 compared with corresponding values for the same genotype mice treated with the same dose of 5-MeO-DMT alone; &P < 0.05 compared with corresponding values for the same genotype mice treated with the same dose of 5-MeO-DMT plus 5 mg/kg harmaline; #P < 0.05 compared with wild-type mice under the same treatment.