PMID- 18980527 OWN - NLM STAT- MEDLINE DCOM- 20090212 LR - 20081104 IS - 0022-3492 (Print) IS - 0022-3492 (Linking) VI - 79 IP - 11 DP - 2008 Nov TI - Lipopolysaccharide-mediated enhancement of bone metabolism in estrogen-deficient mice. PG - 2173-81 LID - 10.1902/jop.2008.070127 [doi] AB - BACKGROUND: Osteoporosis may be a risk factor in periodontal disease. However, biologic mechanisms explaining the apparent interaction between these two diseases have not been defined. It is well known that lipopolysaccharide (LPS) increases the resorption of alveolar bone. We hypothesized that LPS and estrogen deficiency have synergistic effects on bone metabolism and may lead to enhanced bone resorption. METHODS: Eighty 8-week-old female ddY mice were divided into two groups and underwent a sham operation or bilateral ovariectomy. They were maintained for 4 weeks to assess estrogen-deficient bone loss. Osteoblasts and bone marrow cells (BMCs) were collected from ovariectomized (OVX) and sham-operated mice. Osteoclast differentiation in a coculture of osteoblasts and BMCs was investigated by tartrate-resistant acid phosphatase staining. Receptor activator of nuclear factor-kappa B ligand (RANKL) mRNA expression in LPS-treated osteoblasts was investigated using real-time polymerase chain reaction. Interferon-gamma (IFN-gamma) and interleukin (IL)-6 and -10 levels in the culture supernatants were evaluated by enzyme-linked immunosorbent assay. Group means were compared by analysis of variance followed by Tukey's honestly significant difference. RESULTS: There was a significant increase in the number of osteoclasts in LPS-treated cocultures from OVX mice compared to sham controls (P <0.05). RANKL mRNA expression in LPS-treated osteoblasts from OVX mice was greater than in sham mice (P <0.05). In contrast, the production of IFN-gamma in LPS-treated coculture from OVX mice was significantly lower than in sham mice (P <0.05). CONCLUSION: LPS-bearing Gram-negative organisms are abundant in periodontal disease, and the results supported the hypothesis that bone resorption is increased in estrogen-deficient patients. FAU - Fujita, Sachiko AU - Fujita S AD - Department of Periodontology, Aichi-Gakuin University, Nagoya, Japan. FAU - Kikuchi, Takeshi AU - Kikuchi T FAU - Sobue, Takanori AU - Sobue T FAU - Suzuki, Mariyo AU - Suzuki M FAU - Koide, Masanori AU - Koide M FAU - Noguchi, Toshihide AU - Noguchi T LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Periodontol JT - Journal of periodontology JID - 8000345 RN - 0 (Estrogens) RN - 0 (Interleukin-1) RN - 0 (Interleukin-6) RN - 0 (Lipopolysaccharides) RN - 0 (RANK Ligand) RN - 0 (RNA, Messenger) RN - 0 (Tumor Necrosis Factor-alpha) RN - EC 3.1.3.1 (Alkaline Phosphatase) SB - IM MH - Alkaline Phosphatase/*metabolism MH - Animals MH - Bone Remodeling/immunology/*physiology MH - Bone Resorption/immunology/*metabolism MH - Bone and Bones/cytology/*metabolism MH - Estrogens/*deficiency/physiology MH - Female MH - Interleukin-1/metabolism MH - Interleukin-6/metabolism MH - Lipopolysaccharides/*immunology/metabolism MH - Mice MH - Osteoclasts/immunology/physiology MH - Postmenopause/metabolism MH - RANK Ligand/genetics/metabolism MH - RNA, Messenger/analysis MH - Tumor Necrosis Factor-alpha/metabolism EDAT- 2008/11/05 09:00 MHDA- 2009/02/13 09:00 CRDT- 2008/11/05 09:00 PHST- 2008/11/05 09:00 [pubmed] PHST- 2009/02/13 09:00 [medline] PHST- 2008/11/05 09:00 [entrez] AID - 10.1902/jop.2008.070127 [doi] PST - ppublish SO - J Periodontol. 2008 Nov;79(11):2173-81. doi: 10.1902/jop.2008.070127.