Table 2.
Treatment | Surgery |
Two-Way ANOVA (P Value) |
|||
---|---|---|---|---|---|
Sham | Ovx | Sham/Ovx | Veh/pAkk | Interaction | |
Tb N, 1/mm | |||||
Veh | 3.26 ± 0.09 | 3.22 ± 0.15 | NS | NS | NS |
pAkk | 3.07 ± 0.18 | 3.10 ± 0.10 | |||
Tb Sp, mm | |||||
Veh | 0.128 ± 0.001 | 0.126 ± 0.001 | NS | NS | NS |
pAkk | 0.128 ± 0.002 | 128.2 ± 0.001 | |||
Crt Thk, mm | |||||
Veh | 0.197 ± 0.002 | 0.186 ± 0.003 | P ≤ 0.01 | NS | NS |
pAkk | 0.192 ± 0.002 | 0.184 ± 0.002 | |||
Femur length, mm | |||||
Veh | 15.37 ± 0.15 | 15.61 ± 0.08 | NS | P ≤ 0.05 | NS |
pAkk | 15.19 ± 0.07 | 15.27 ± 0.13 |
Twelve-week-old female mice were treated with either vehicle (Veh) or pasteurized Akkermansia muciniphila (pAkk) by daily oral gavage during 28 days, starting 3 days before ovariectomy (Ovx) or sham surgery. At the end of the experiment, dissected femurs were analyzed with high-resolution μCT. Trabecular number (Tb N), trabecular separation (Tb Sp), cortical thickness (Crt Thk), and femur length were analyzed. Values are given as means ± SE, (n = 8–12). Two-way ANOVA to test the effect of treatment (Veh/pAkk) and surgical procedure (Sham/Ovx) and their interaction was used.