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肾素抑制可改善小鼠卵巢切除诱导的腰椎骨质疏松症。

Renin inhibition improves ovariectomy-induced osteoporosis of lumbar vertebra in mice.

作者信息

Zhang Fang-Yi, Yang Feng-Jian, Yang Jiu-Lin, Wang Liang, Zhang Yan

机构信息

Center for Systems Biomedical Sciences, University of Shanghai for Science and Technology; Shanghai 200093, China.

出版信息

Biol Pharm Bull. 2014;37(12):1994-7. doi: 10.1248/bpb.b14-00576.

Abstract

The skeletal renin–angiotensin system (RAS) is involved in the progression of osteoporosis and the active peptide within the RAS, angiotensin II (ANG II), has deleterious effects on bones. This study was performed to investigate whether suppression of the rate-limiting step of the RAS cascade by the renin inhibitor aliskiren has a benefit on trabecular bone in osteoporotic mice. A postmenopausal osteoporosis model was induced by bilateral ovariectomy. The ovariectomized (OVX) mice were treated with a low (5 mg/kg) or high (25 mg/kg) dose of aliskiren for 6 weeks. Micro-computed tomography was performed to detect trabecular bone parameters of lumbar vertebra and to obtain 3-dimensional (3D) images. Treatment with aliskiren markedly increased bone volume over total volume (p<0.05), trabecular bone number (p<0.05), connectivity density (p<0.05), and bone mineral density (p<0.05) and reduced trabecular bone separation (p<0.05) compared to vehicle-treated OVX mice. Similarly, the 3D images were consistent with the quantitative data that showed aliskiren could markedly reverse the ovariectomy-induced pathological changes of trabecular bone. Thus, this study indicated that the treatment of estrogen-deficient mice with aliskiren could markedly increase bone mass and improve trabecular bone structure, suggesting its potential application in treating postmenopausal osteoporosis.

摘要

骨骼肾素-血管紧张素系统(RAS)参与骨质疏松症的进展,RAS中的活性肽血管紧张素II(ANG II)对骨骼具有有害作用。本研究旨在探讨肾素抑制剂阿利吉仑对RAS级联反应限速步骤的抑制是否对骨质疏松小鼠的小梁骨有益。通过双侧卵巢切除术诱导建立绝经后骨质疏松模型。对去卵巢(OVX)小鼠给予低剂量(5 mg/kg)或高剂量(25 mg/kg)阿利吉仑治疗6周。采用微型计算机断层扫描技术检测腰椎小梁骨参数并获取三维(3D)图像。与给予赋形剂处理的OVX小鼠相比,阿利吉仑治疗显著增加了骨体积分数(p<0.05)、小梁骨数量(p<0.05)、连接密度(p<0.05)和骨矿物质密度(p<0.05),并减少了小梁骨间距(p<0.05)。同样,3D图像与定量数据一致,表明阿利吉仑可显著逆转卵巢切除诱导的小梁骨病理变化。因此,本研究表明,用阿利吉仑治疗雌激素缺乏小鼠可显著增加骨量并改善小梁骨结构,提示其在治疗绝经后骨质疏松症方面具有潜在应用价值。

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