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Rosiglitazone disrupts endosteal bone formation during distraction osteogenesis by local adipocytic infiltration

Rosiglitazone (Rosi) is a drug in the thiazolidinedione class for treatment of Type 2 diabetes mellitus (T2DM), which binds and activates PPARγ nuclear receptor in fat cells, sensitizing them to insulin. Despite proven antidiabetic efficacy, Rosi therapy may be associated with trabecular bone loss a...

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Main Authors: Liu, Lichu, Aronson, James, Lecka-Czernik, Beata
Formato: Artigo
Idioma:Inglês
Publicado: 2012
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3513662/
https://ncbi.nlm.nih.gov/pubmed/23069375
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2012.09.038
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