4.8 Editorial Material

From the gut to the strut: where inflammation reigns, bone abstains

Journal

JOURNAL OF CLINICAL INVESTIGATION
Volume 126, Issue 6, Pages 2045-2048

Publisher

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI87430

Keywords

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Funding

  1. NIAMS NIH HHS [R01 AR065932, R01 AR067066] Funding Source: Medline
  2. NIA NIH HHS [R01 AG040132, R01 AG023176] Funding Source: Medline

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In this issue of the JCI, Li et al. show that germ-free mice, when chemically castrated, do not lose bone - a finding that unequivocally establishes a role of gut microbiota in mediating hypogonadal bone loss. Additionally and not unexpectedly, probiotics reversed hypogonadal osteopenia in sex steroid-deficient mice by preventing the disruption of gut barrier function and dampening cytokine-induced inflammation. The authors propose that TNF alpha is a key mediator; however, it is very likely that other molecules - including IL-1, IL-6, IL-17, RANKL, OPG, and CCL2 - modulate probiotic action. The results of this study highlight the potential for repurposing probiotics for the therapy of osteoporosis. Future placebo-controlled clinical trials will be required to establish safety and efficacy of probiotics in reducing fracture risk in people.

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