Skip to main content
. 2019 Apr 9;10:347. doi: 10.3389/fphar.2019.00347

Table 2.

Maximum G-protein efficacy (Emax ± SEM) and potency (EC50 ± SEM) of 14-O-MeM6SU, compared to morphine and fentanyl in vehicle (non-diabetic) and 9 and 12 weeks STZ (diabetic) treated rat brain performed in [35S]GTPγS binding assays.

Emax ± SEM (%) EC50 ± SEM (nM)


Non-diabetic Diabetic Non-diabetic Diabetic
9 weeks
14-O-MeM6SU 145.7 ± 2.4### (n = 6) 140.7 ± 2.1 (n = 6) 29.51 ± 11.44 (n = 6) 33.19 ± 19.09 (n = 6)
Fentanyl 140.2 ± 2.67## (n = 7) 134.8 ± 2.84 (n = 5) 36.64 ± 18.42 (n = 7) 32.02 ± 20.14 (n = 5)
Morphine 128.8 ± 2.65 (n = 7) 133.5 ± 4.85 (n = 6) N.D.1 N.D.1
12 weeks
14-O-MeM6SU 148.5 ± 3.59## (n = 4) 146.1 ± 3.22# (n = 5) 34.99 ± 17.74 (n = 4) 27.86 ± 13.87 (n = 5)
Fentanyl 149.7 ± 2.38## (n = 5) 146.1 ± 3.51# (n = 4) 197.7 ± 54.05+ (n = 5) 124.74 ± 55.64 (n = 4)
Morphine 135.2 ± 2.65 (n = 4) 135.6 ± 3.08 (n = 4) N.D.1 N.D.1

Values were calculated according to Figure 9. #Indicates the significant difference compared to morphine within control or diabetic samples (#P < 0.05; ##P < 0.01; ###P < 0.001). +indicates the significant difference compared to 14-O-MeM6SU within control or diabetic samples (+P < 0.05). 1Not determined, since the EC50 values could not be interpreted. Two-way ANOVA followed by Fisher’s LSD post hoc test.