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Pulsed electromagnetic fields protect the balance between adipogenesis and osteogenesis on steroid-induced osteonecrosis of femoral head at the pre-collapse stage in rats

机译:在塌陷前,脉冲电磁场​​可保护类固醇激素引起的股骨头坏死对脂肪形成和成骨的影响。

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This study was designed to investigate the effects of pulsed electromagnetic fields (PEMF) on the balance of adipogenesis and osteogenesis on steroid-induced osteonecrosis of the femoral head (OFH) in rats. Forty-two rats were divided into three groups: Steroid group (S, n=16); Steroid+PEMF group (S+P, n=16); and Control group (C, n=10). For groups S and S+P, all rats were first intravenously given 10μg/kg lipopolysaccharide on day 1, and then intramuscularly injected with 20mg/kg methylprednisolone acetate on days 2, 3, and 4, with an interval of 24h. After 4 weeks, the S+P group was treated with PEMF (4.5-ms square pulse, repeated at 15Hz, with a peak of 1.2mT) for 4h a day for the next 8 weeks. Group S was not exposed to PEMF. Group C was chosen as the control group, without steroid use and exposure to PEMF. After 8 weeks of treatment, the histological changes, and mRNA and protein expressions of PPAR-γ2 and Runx2 were measured and analyzed. Compared with the S group, lower incidence of osteonecrosis (31% vs. 69%, P<0.05) and empty osteocyte lacuna rate (36.16±15.34 vs. 59.55±21.70, P<0.01) was observed in the S+P group. Furthermore, PEMF suppressed the expressions of PPAR-γ2 and improved the expressions of Runx2 in the femoral head (P<0.05). All data suggest that PEMF is an effective physiotherapy in the treatment of steroid-induced ONFH, and the possible underlying mechanisms include protecting the balance between adipogenesis and osteogenesis.
机译:本研究旨在研究脉冲电磁场​​(PEMF)对类固醇引起的股骨头坏死(OFH)大鼠脂肪形成和成骨的平衡的影响。 42只大鼠分为三组:类固醇组(S,n = 16);激素组(S,n = 16)。类固醇+ PEMF组(S + P,n = 16);对照组(C,n = 10)。对于S组和S + P组,首先在第1天给所有大鼠静脉注射10μg/ kg脂多糖,然后在第2、3和4天以24h的间隔肌注20mg / kg乙酸甲基泼尼松龙。 4周后,在接下来的8周中,每天用PEMF(4.5 ms方波,以15Hz重复,峰值为1.2mT)对S + P组进行每天4h的治疗。 S组未暴露于PEMF。选择C组作为对照组,不使用类固醇且不暴露于PEMF。治疗8周后,测量并分析PPAR-γ2和Runx2的组织学变化以及mRNA和蛋白质表达。与S组相比,S + P组的骨坏死发生率较低(31%vs. 69%,P <0.05)和空骨细胞腔隙率(36.16±15.34 vs. 59.55±21.70,P <0.01)。此外,PEMF抑制了股骨头中PPAR-γ2的表达,并改善了Runx2的表达(P <0.05)。所有数据表明,PEMF是治疗类固醇诱导的ONFH的有效物理疗法,可能的潜在机制包括保护脂肪形成和成骨之间的平衡。

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