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首页> 外文期刊>The British Journal of Nutrition >Synergistic attenuation of ovariectomy-induced bone loss by combined use of fish oil and 17 ss-oestradiol
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Synergistic attenuation of ovariectomy-induced bone loss by combined use of fish oil and 17 ss-oestradiol

机译:通过联合使用鱼油和 17 ss-雌二醇协同减弱卵巢切除术引起的骨质流失

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摘要

Oestrogen and n-3 PUFA, especially EPA and DHA, have been reported to have beneficial effects on bone loss. Thus, the purpose of the present study was to investigate the synergistic bone-protective mechanism of combined treatments of EPA + DHA supplementation and oestrogen injection in ovariectomised rats. Rats were fed a modified American Institute of Nutrition-93G diet with 0, 1 or 2 n-3 PUFA (EPA + DHA) relative to the total energy intake for 12 weeks. Rats were surgically ovariectomised at week 8, and after a 1-week recovery period rats were injected with either 17 ss-oestradiol-3-benzoate (E-2) or maize oil for the last 3 weeks. Combined use of n-3 PUFA and E-2 synergistically increased femoral cortical bone volume, bone mineral content and the bone expression of runt-related transcription factor 2 (RUNX2), but decreased the bone expression of IL-1 ss. Both n-3 PUFA and E-2 decreased the bone expressions of IL-7, TNF-alpha and PPAR-gamma, and increased the bone expression of oestrogen receptor-alpha. n-3 PUFA in the presence of E-2 and E-2 alone significantly decreased the bone expressions of IL-1 ss and IL-6 and increased the bone expression of RUNX2. E-2 significantly decreased the serum levels of bone turnover markers and the bone expression of receptor activator of NF-kappa B ligand, but decreased the bone expression of osteoprotegerin. The combined use of n-3 PUFA and E-2 exerted synergistic bone-protective efficacy through up-regulation of RUNX2, an essential transcription factor for bone formation, as well as the suppression of bone-resorbing cytokine IL-1 ss.
机译:据报道,雌激素和 n-3 PUFA,尤其是 EPA 和 DHA,对骨质流失有益。因此,本研究的目的是探讨EPA+DHA补充和雌激素注射联合治疗卵巢切除大鼠的协同骨保护机制。给大鼠喂食改良的美国营养研究所-93G饮食,相对于总能量摄入量为0%,1%或2%n-3 PUFA(EPA + DHA),持续12周。大鼠在第8周进行手术卵巢切除术,在1周的恢复期后,大鼠在最后3周内注射17 ss-雌二醇-3-苯甲酸酯(E-2)或玉米油。n-3 PUFA 和 E-2 联合使用可协同增加股骨皮质骨体积、骨矿物质含量和矮幅相关转录因子 2 (RUNX2) 的骨表达,但降低 IL-1 ss 的骨表达。n-3 PUFA和E-2均降低IL-7、TNF-α和PPAR-γ的骨表达,增加雌激素受体-α的骨表达。单独使用E-2和E-2的n-3 PUFA显著降低了IL-1 ss和IL-6的骨表达,增加了RUNX2的骨表达。E-2显著降低血清骨转换标志物水平和NF-κB配体受体激活剂的骨表达,但降低骨保护素的骨表达。n-3 PUFA 和 E-2 的联合使用通过上调 RUNX2(骨形成的必需转录因子)以及抑制骨吸收细胞因子 IL-1 ss 发挥了协同的骨保护功效。

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