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. 2016 Jun 1;157(8):3242–3252. doi: 10.1210/en.2016-1181

Table 4.

Effect of E2 on Trabecular Bone Mass in POMC-ERα−/− Mice

Control
POMC-ERα−/−
OVX OVX + E2 OVX OVX + E2
Femur
    BV/TV (%) 9.5 ± 1.0 39.8 ± 1.9c 9.2 ± 1.0 47.4 ± 2.0c,d
    Tb.N (L/mm) 2.4 ± 0.2 9.6 ± 0.4c 2.3 ± 0.2 10.6 ± 0.6c
    Tb.Th (μm) 39 ± 1 42 ± 1 40 ± 1 45 ± 2
    Tb.Sp (μm) 132 ± 1 74 ± 5c 132 ± 1 60 ± 5c
Vertebrae L5
    BV/TV (%) 15.7 ± 1.1 26.8 ± 1.6c 16.4 ± 1.7 34.2 ± 2.8b
    Tb.N (L/mm) 4.1 ± 0.3 6.3 ± 0.4b 3.9 ± 0.5 8.1 ± 1.0a
    Tb.Th (μm) 39 ± 1 43 ± 1a 42 ± 1 43 ± 3
    Tb.Sp (μm) 71 ± 3 59 ± 2a 74 ± 5 50 ± 4b

High-resolution μCT analysis of BV/TV, trabecular number (Tb. N), trabecular thickness (Tb.Th), and trabecular separation (Tb.Sp) in femur (n = 7–10) and vertebrae L5 (n = 4–6) of OVX POMC-ERα−/− and OVX control mice treated with either E2 (0.5 μg/d) or vehicle. Data are presented as mean ± SEM.

a

P < .05 E2 treated vs vehicle treated, Student's t test.

b

P < .01 E2 treated vs vehicle treated, Student's t test.

c

P < .001 E2 treated vs vehicle treated, Student's t test.

d

P < .05 E2 effect in POMC-ERα−/− mice vs E2 effect in control mice (interaction term from two-way ANOVA).