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Siddhartha Mukherjee, Noopur Raje, Jesse A. Schoonmaker, Julie C. Liu, Teru Hideshima, Marc N. Wein, Dallas C. Jones, Sonia Vallet, Mary L. Bouxsein, Samantha Pozzi, Shweta Chhetri, Y. David Seo, Joshua P. Aronson, Chirayu Patel, Mariateresa Fulciniti, Louise E. Purton, Laurie H. Glimcher, Jane B. Lian, Gary Stein, Kenneth C. Anderson, David T. Scadden
Published in Volume 118, Issue 2
J Clin Invest. 2008; 118(2):491–504 doi:10.1172/JCI33102
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Figure 7
Bzb rescues osteoporosis in ovariectomized mice.

FVB/N female mice were ovariectomized at week 9 and treated with saline or 0.3 mg/kg Bzb for 6 weeks (18 doses) starting at week 11.5. (A) Representative micro-CT analysis of cross sections of trabecular bone are shown for mock-treated, ovariectomized, and ovariectomized/Bzb-treated mice. Scale bar: 1.0 mm. (B) Baseline distal femur BMD increased upon Bzb treatment in both mock-treated and ovariectomized mice. *P = 0.006; **P = 0.03; n = 10 femurs/group. Quantitative analysis by micro-CT scanning revealed that ovariectomized animals had decreases in trabecular bone volume fraction and that Bzb treatment partly rescued this decrease. P = 0.001; P = 0.01; n = 10 femurs/group. Trabecular number/mm decreased with ovariectomy but was rescued by Bzb treatment. ζP = 0.01; ΧP = 0.002; n = 10 femurs/group. (C) BFR per BSpm (BFR/B pm) was increased in ovary-intact animals by Bzb treatment (#P = 0.007; n = 7 femurs) and also increased in ovariectomized animals (††P = 0.05; n = 7 femurs). (D) Mineral apposition rate was increased in ovary-intact animals (‡‡P = 0.01; n = 7 femurs) with Bzb treatment. In ovariectomized animals, there was increased mineral apposition, but the effect was not significant. P = 0.1.