血管紧张素-(1-7)通过调节有机基质对糖尿病大鼠骨基质质量的潜在预防作用。

IF 1.9 Q2 ORTHOPEDICS
Ugur Dalaman, Ibrahim Cuneyit, Şevval Öztürk, Ege Rıza Karagur, Mert Ocak, Nazmi Yaras, Mustafa Unal, Baris Ozgur Donmez
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引用次数: 0

摘要

目的:本实验旨在探讨血管紧张素(1-7)(Ang-[1-7])对糖尿病大鼠骨组织微观结构、生物力学和生物理化性质的影响。材料与方法:选用雄性Wistar大鼠48只,3月龄,体重280 ~ 330 g。将大鼠分为4组,每组12只:对照组、糖尿病组、DM-Ang-(1-7)、Ang-(1-7)。通过显微计算机断层扫描(CT)、拉曼光谱和三点弯曲生物力学测试对样品进行分析。结果:糖尿病显著损害骨质量,降低皮质厚度、最大负荷和弯曲强度(结论:这些发现表明Ang-(1-7)对糖尿病大鼠骨矿物质的影响最小。然而,在该模型中,它可能对骨有机基质内的三螺旋结构损伤有潜在的预防作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Potential preventive effects of angiotensin-(1-7) on bone matrix quality in diabetic rats through modulation of the organic matrix.

Potential preventive effects of angiotensin-(1-7) on bone matrix quality in diabetic rats through modulation of the organic matrix.

Potential preventive effects of angiotensin-(1-7) on bone matrix quality in diabetic rats through modulation of the organic matrix.

Potential preventive effects of angiotensin-(1-7) on bone matrix quality in diabetic rats through modulation of the organic matrix.

Objectives: This experimental study aims to investigate the effects of angiotensin (1-7) (Ang-[1-7]) on the microstructural, biomechanical, and biophysicochemical properties of bone tissue in diabetic rats.

Materials and methods: Forty-eight male Wistar rats, aged three months and weighing between 280 and 330 g, were used in this study. Four groups, each containing 12 rats, were established: Control, diabetes mellitus (DM), DM-Ang-(1-7), and Ang-(1-7). The samples underwent analysis through micro-computed tomography (CT), Raman spectroscopy, and three-point bending biomechanical test.

Results: Diabetes significantly impaired bone quality, with reduced cortical thickness, maximum load, and flexural strength (p<0.05). The Ang-(1-7) treatment improved flexural strength (p<0.05), but did not fully restore mechanical function. Micro-CT showed decreased bone volume and trabecular thickness in both diabetic groups (p<0.05), with no significant recovery by Ang-(1-7). Raman spectroscopy revealed lower mineral-to-matrix ratio and disrupted collagen quality in diabetic bone (p<0.05), while Ang-(1-7) partially restored collagen-related parameters.

Conclusion: These findings highlight that Ang-(1-7) has minimal impact on bone minerals in DM rats. However, it may have a potential preventive effect on the triple-helix structural impairment within the bone organic matrix in this model.

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