首页> 外文期刊>Life sciences >Moderate hyperhomocysteinemia induced by short-term dietary methionine overload alters bone microarchitecture and collagen features during growth
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Moderate hyperhomocysteinemia induced by short-term dietary methionine overload alters bone microarchitecture and collagen features during growth

机译:短期膳食蛋氨酸诱导的中度高血栓血症过载改变了骨微体系结构和生长期间的胶原特征

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摘要

Abstract Aims In general, hyperhomocysteinemia is increasingly appreciated as a risk factor for various diseases, including osteoporosis. However, its effects in non-adults remain largely unknown. Our aim was to determine whether dietary-caused increased homocysteine levels have deleterious effects on bone structure during growth. Main methods We developed a model of moderate hyperhomocysteinemia caused by short-term methionine nutritional overload in growing rats. 30-days-old male Wistar albino rats were randomly assigned to either experimental group subject to a 30-days hypermethionine diet or control group. High-resolution 3D assessment of bone geometry and microarchitecture, as well as fluorescence spectroscopic analysis of bone matrix were performed. Key findings Short-term moderate hyperhomocysteinemia (~30μmol/L) achieved in the study notably affected bone and cartilage characteristics. Parameters of the cortical bone geometry in the experimental group indicated peculiar reorganization of the bone cross-section. Trabecular bone microarchitecture was especially sensitive to hyperhomocysteinemia showing clearly negative bone balance in the experimental group (almost 30% reduced bone volume, mainly due to ~25% decrease in trabecular number as well as markedly reduced trabecular connections). Fluorescent spectroscopy of bone matrix revealed multiple alterations to collagen spectra due to homocysteine accumulation in bone, indicative of broken collagenous cross-links. Significance Given that appropriate accrual of bone mass during growth has important effects on the risk of osteoporosis in adulthood, understanding the skeletal effects of dietary-induced hyperhomocysteinemia in non-adults is essential for interpreting its importance as a modifiable risk factor for osteoporosis and improving programs to preserve/re-establish bone health. Graphical abstract Display Omitted
机译:摘要旨在一般来说,高管抑制因素越来越欣赏各种疾病的危险因素,包括骨质疏松症。然而,其在非成年人中的效果仍然很大程度上是未知的。我们的目的是确定膳食导致的同型同型半胱氨酸水平是否对生长期间对骨骼结构具有有害影响。主要方法我们开发了一种中度高血管脂质症的模型,由短期甲硫氨酸营养过载在生长大鼠中引起的。将30天龄雄性Wistar白化大鼠随机分配给实验组,约为30天的高血硫饮食或对照组。进行骨几何和微体系结构的高分辨率3D评估,以及骨基质的荧光光谱分析。主要发现短期中度高血细胞症(〜30μmol/ L)在研究中达到了显着影响骨和软骨特性。实验组皮质骨几何体的参数表明骨横截面的特殊重组。小梁骨微架构对实验组中明显阴性骨平衡显示出明显阴性骨骼平衡(骨体积降低的几乎30%,主要是由于豆间数减少约25%,并且显着降低了短边颌骨连接)。由于骨中的骨囊积累,骨基质的荧光光谱揭示了对胶原纤维的多种改变,指示破碎的胶原交联。鉴于增长过程中骨质量的适当应计对成年骨质疏松症风险的重要性,了解膳食诱导的非成年人的高管抑菌症的骨骼效应对于解释其重要性作为骨质疏松症和改善计划的可改性危险因素至关重要保持/重新建立骨骼健康。省略了图形抽象显示

著录项

  • 来源
    《Life sciences》 |2017年第2017期|共8页
  • 作者单位

    Laboratory for Anthropology Institute of Anatomy Faculty of Medicine University of Belgrade;

    Laboratory for Neurophysiology Institute of Medical Physiology “Richard Burian” Faculty of;

    Department of Life Sciences Institute for Multidisciplinary Research University of Belgrade;

    Department of Life Sciences Institute for Multidisciplinary Research University of Belgrade;

    Department of Life Sciences Institute for Multidisciplinary Research University of Belgrade;

    Laboratory for Anthropology Institute of Anatomy Faculty of Medicine University of Belgrade;

    Laboratory for Neurophysiology Institute of Medical Physiology “Richard Burian” Faculty of;

    Laboratory for Neurophysiology Institute of Medical Physiology “Richard Burian” Faculty of;

    Laboratory for Neurophysiology Institute of Medical Physiology “Richard Burian” Faculty of;

    Laboratory for Anthropology Institute of Anatomy Faculty of Medicine University of Belgrade;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
  • 关键词

    Bone; Homocysteine; Fluorescent spectroscopy; Development; Tissue microarchitecture; Collagen;

    机译:骨;同型半胱氨酸;荧光光谱;发展;组织微体系结构;胶原蛋白;

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