Effects of Lobeglitazone, a New Thiazolidinedione, on Osteoblastogenesis and Bone Mineral Density in Mice
| Autor: | Hyo Jin Maeng, Gha Young Lee, Soo Lim, Hyun Jin Jin, Seo Yeon Lee, Kyoung Min Kim, Tae Jung Oh, Sung Hee Choi, Hak Chul Jang |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
musculoskeletal diseases medicine.medical_specialty Bone density medicine.drug_class Endocrinology Diabetes and Metabolism Lobeglitazone 030209 endocrinology & metabolism lcsh:Diseases of the endocrine glands. Clinical endocrinology 03 medical and health sciences 0302 clinical medicine Endocrinology Bone and bones Internal medicine medicine Endocrine Research Thiazolidinedione Bone mineral Osteoblasts lcsh:RC648-665 biology Osteoblast 030104 developmental biology medicine.anatomical_structure Osteocalcin biology.protein Original Article Thiazolidinediones Rosiglitazone Pioglitazone medicine.drug |
| Zdroj: | Endocrinology and Metabolism, Vol 32, Iss 3, Pp 389-395 (2017) Endocrinology and Metabolism |
| ISSN: | 2093-5978 |
| Popis: | Background Bone strength is impaired in patients with type 2 diabetes mellitus despite an increase in bone mineral density (BMD). Thiazolidinedione (TZD), a peroxisome proliferator activated receptor γ agonist, promotes adipogenesis, and suppresses osteoblastogenesis. Therefore, its use is associated with an increased risk of fracture. The aim of this study was to examine the in vitro and in vivo effects of lobeglitazone, a new TZD, on bone. Methods MC3T3E1 and C3H10T1/2 cells were cultured in osteogenic medium and exposed to lobeglitazone (0.1 or 1 μM), rosiglitazone (0.4 μM), or pioglitazone (1 μM) for 10 to 14 days. Alkaline phosphatase (ALP) activity, Alizarin red staining, and osteoblast marker gene expression were analyzed. For in vivo experiments, 6-month-old C57BL/6 mice were treated with vehicle, one of two doses of lobeglitazone, rosiglitazone, or pioglitazone. BMD was assessed using a PIXImus2 instrument at the baseline and after 12 weeks of treatment. Results As expected, in vitro experiments showed that ALP activity was suppressed and the mRNA expression of osteoblast marker genes RUNX2 (runt-related transcription factor 2) and osteocalcin was significantly attenuated after rosiglitazone treatment. By contrast, lobeglitazone at either dose did not inhibit these variables. Rosiglitazone-treated mice showed significantly accelerated bone loss for the whole bone and femur, but BMD did not differ significantly between the lobeglitazone-treated and vehicle-treated mice. Conclusion These findings suggest that lobeglitazone has no detrimental effects on osteoblast biology and might not induce side effects in the skeletal system. |
| Databáze: | OpenAIRE |
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