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雌激素缺乏导致骨质疏松症时骨组成、结构和强度的时间变化。

Temporal changes in bone composition, architecture, and strength following estrogen deficiency in osteoporosis.

机构信息

Department of Anatomy, Royal College of Surgeons in Ireland, 123, St. Stephen's Green, Dublin 2, Ireland.

出版信息

Calcif Tissue Int. 2012 Dec;91(6):440-9. doi: 10.1007/s00223-012-9657-7. Epub 2012 Oct 18.


DOI:10.1007/s00223-012-9657-7
PMID:23076448
Abstract

Using an ovariectomized (OVX) ovine model, we provide an analysis of the timing of changes in bone following estrogen deficiency. The expression of genes known to regulate osteoclastogenesis, matrix production, and mineralization, as measured by real-time RT-PCR, was significantly increased by 12 months; and increased expression was maintained through to 31 months post-OVX compared to controls. FTIR spectroscopy confirmed that mineralized crystals were less mature than in controls 12 months post-OVX and were even less so by 31 months. The mineral-to-matrix ratio was significantly reduced by 31 months, while the ratio of mature to immature collagen cross-linking was initially increased at 12 months and subsequently reduced at 31 months post-OVX. In contrast, trabecular number, thickness, and separation were unchanged at 12 months. Significant reductions in trabecular number and thickness and a significant increase in trabecular separation were observed 31 months after OVX. Most notably perhaps these combined changes led to a significant reduction in the compressive strength of trabecular bone after 31 months. The results indicate that there is an initial increase in bone turnover, which is accompanied by a change in bone composition. This is followed by a continued increase in bone resorption and relative reduction in bone formation, leading to deterioration in bone microarchitecture. Ultimately, these cumulative changes led to a significant reduction in the compressive strength of bones following 31 months of estrogen deficiency. These findings provide important insight into the time sequence of changes during osteoporosis.

摘要

我们采用去卵巢(OVX)绵羊模型,分析了雌激素缺乏后骨变化的时间进程。通过实时 RT-PCR 测定,已知调节破骨细胞生成、基质生成和矿化的基因的表达在 12 个月时显著增加;与对照组相比,这种增加的表达在去卵巢后 31 个月时仍得以维持。傅里叶变换红外光谱(FTIR)分析证实,去卵巢 12 个月后矿化晶体的成熟度低于对照组,31 个月时甚至更低。31 个月时,矿物质与基质的比值显著降低,而成熟与不成熟胶原交联的比值在 12 个月时最初增加,随后在 31 个月时降低。相比之下,12 个月时,小梁数量、厚度和分离度无变化。去卵巢 31 个月后,小梁数量、厚度显著减少,小梁分离度显著增加。也许最值得注意的是,这些综合变化导致去卵巢 31 个月后小梁骨的抗压强度显著降低。结果表明,骨转换最初增加,同时伴有骨成分的变化。随后,骨吸收持续增加,骨形成相对减少,导致骨微结构恶化。最终,这些累积变化导致去卵巢 31 个月后骨的抗压强度显著降低。这些发现为骨质疏松症发生过程中的时间顺序变化提供了重要的见解。

相似文献

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Temporal changes in bone composition, architecture, and strength following estrogen deficiency in osteoporosis.

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[2]
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Int J Mol Sci. 2022-8-10

[3]
Osteocytes and Estrogen Deficiency.

Curr Osteoporos Rep. 2021-12

[4]
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Curr Osteoporos Rep. 2021-10

[5]
A Novel 3D Osteoblast and Osteocyte Model Revealing Changes in Mineralization and Pro-osteoclastogenic Paracrine Signaling During Estrogen Deficiency.

Front Bioeng Biotechnol. 2020-6-10

[6]
Determinants of Bone Health Status in a Multi-Ethnic Population in Klang Valley, Malaysia.

Int J Environ Res Public Health. 2020-1-7

[7]
Secondary alterations in bone mineralisation and trabecular thickening occur after long-term estrogen deficiency in ovariectomised rat tibiae, which do not coincide with initial rapid bone loss.

Osteoporos Int. 2020-3

[8]
Analysis of microscopic bone properties in an osteoporotic sheep model: a combined biomechanics, FE and ToF-SIMS study.

J R Soc Interface. 2019-2-28

[9]
Estrogen deficiency impairs integrin αβ-mediated mechanosensation by osteocytes and alters osteoclastogenic paracrine signalling.

Sci Rep. 2019-3-15

[10]
Preclinical and Translational Studies in Small Ruminants (Sheep and Goat) as Models for Osteoporosis Research.

Curr Osteoporos Rep. 2018-4

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