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Evidence for Osteocalcin Production by Adipose Tissue and Its Role in Human Metabolism

机译:脂肪组织产生骨钙素的证据及其在人体代谢中的作用

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Context: The adipose tissue (AT), which is an endocrine organ, is linked to several metabolic abnormalities. Undercarboxylated osteocalcin (ucOCN) regulates insulin and adiponectin secretion.Objective: Our objective was to investigate the involvement of OCN in obesity and to evaluate, in vitro and ex vivo , the role of AT in the modulation of this endocrine circuit.Design, Patients, and Setting: This transversal study involved 83 male subjects, divided according to the World Health Organization body mass index classification, evaluated at Padova’s Obesity Outpatient Clinic.Methods: OCN, both undercarboxylated (ucOCN) and carboxylated (cOCN) forms, was measured in serum by ELISA. OCN mRNA expression and protein production were measured by quantitative RT-PCR and immunohistochemistry during in vitro adipogenesis and in sc AT (SAT) and omental AT (OAT) from normal adult men. cOCN and ucOCN release by AT in a simple growth medium was verified by ELISA.Results: Overweight and obese patients had a lower ucOCN and ucOC/OCN ratio. In the whole cohort, ucOCN/OCN ratio was negatively correlated to body mass index (ρ = ?0.233; P < 0.05). OCN mRNA was present in SAT and OAT and during all stages of adipogenesis, with higher expression in the first steps. Immunohistochemistry confirmed the expression of OCN protein. Both SAT and OAT were able to release cOCN and ucOCN.Conclusions: Our data support a pathophysiological link between ucOCN and cOCN balance and obesity. OCN is present in the first phases of adipogenesis but also in human AT ex vivo . AT releases, in vitro , both ucOCN and cOCN, suggesting a possible link between AT and OCN in the regulation of metabolism.
机译:背景:作为内分泌器官的脂肪组织(AT)与多种代谢异常有关。羧基不足的骨钙素(ucOCN)调节胰岛素和脂联素的分泌。背景:这项横向研究涉及83位男性受试者,根据世界卫生组织的体重指数分类,在帕多瓦肥胖门诊诊所进行了评估。方法:在血清中测量了OCN(羧基不足(ucOCN)和羧基(cOCN)形式)通过ELISA。在体外成脂过程中以及正常成年男子的sc AT(SAT)和网膜AT(OAT)中,通过定量RT-PCR和免疫组织化学测量了OCN mRNA表达和蛋白质产生。通过ELISA验证了AT在简单的生长培养基中释放的cOCN和ucOCN。结果:超重和肥胖患者的ucOCN和ucOC / OCN比率较低。在整个队列中,ucOCN / OCN比值与体重指数呈负相关(ρ=±0.233; P <0.05)。 OCN mRNA存在于SAT和OAT中以及成脂的所有阶段,在第一步中表达较高。免疫组织化学证实了OCN蛋白的表达。 SAT和OAT均能够释放cOCN和ucOCN。结论:我们的数据支持ucOCN与cOCN平衡与肥胖之间的病理生理联系。 OCN存在于脂肪形成的第一阶段,也存在于人AT体内。 AT在体外释放ucOCN和cOCN,这表明AT和OCN之间可能在代谢调节方面存在联系。

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