{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,8]],"date-time":"2026-07-08T10:21:49Z","timestamp":1783506109361,"version":"3.55.0"},"reference-count":59,"publisher":"Bioscientifica","issue":"3","funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["AR060913"],"award-info":[{"award-number":["AR060913"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["journals.bioscientifica.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2025,3,1]]},"abstract":"<jats:p>Leptin increases focal inflammation and osteolysis induced by polyethylene particles in leptin-deficient ob\/ob mice, suggesting that this adipokine, an important immune modulator, contributes to orthopedic implant failure. Focal inflammation leads to bone loss at distant skeletal sites, and it is plausible that leptin also contributes to this response. We tested this possibility in 6-week-old female ob\/ob mice (6\u20138\/group) by evaluating bone architecture, turnover and gene expression 12 days following the surgical placement of polyethylene particles over the calvaria. Particle treatment had minimal effect on bone mass, density or cancellous bone architecture in the femur and 5th lumbar vertebra (LV). However, compared to controls, particle treatment altered tibial expression levels of 32\/84 genes related to bone metabolism. Subcutaneous infusion of leptin (6 \u03bcg\/d) to mice following the placement of polyethylene particles over the calvaria (combination treatment) resulted in cancellous bone loss in the distal femur metaphysis and LV and in the differential expression of 34\/84 genes, 15 of which overlapped with particle treatment. Notably, combination treatment, but not particle treatment, resulted in increased expression of genes strongly associated with bone turnover and response to inflammation. Leptin treatment alone (0.1\u201310 \u03bcg\/day) did not result in bone loss in the femur or LV in the ob\/ob mice. These findings suggest that leptin exaggerates the detrimental effects of particle-induced inflammation on bone turnover balance, leading to systemic bone loss.<\/jats:p>","DOI":"10.1530\/joe-24-0324","type":"journal-article","created":{"date-parts":[[2025,1,30]],"date-time":"2025-01-30T07:00:38Z","timestamp":1738220438000},"update-policy":"https:\/\/doi.org\/10.1530\/crossmarkpolicy-5","source":"Crossref","is-referenced-by-count":2,"title":["Leptin potentiates bone loss at skeletal sites distant from focal inflammation in female\n                    <i>ob\/ob<\/i>\n                    mice"],"prefix":"10.1530","volume":"264","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3031-0398","authenticated-orcid":true,"given":"Russell T","family":"Turner","sequence":"first","affiliation":[{"name":"Skeletal Biology Laboratory, School of Nutrition and Public Health, Oregon State University 1 , , ,","place":["Corvallis, Oregon, USA"]},{"name":"Center for Healthy Aging Research, Oregon State 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