唑来膦酸和心得安联合治疗可改善绝经后骨质疏松大鼠模型的骨小梁微结构和力学性能。

IF 1.1 Q3 ORTHOPEDICS Journal of Osteoporosis Pub Date : 2014-01-01 Epub Date: 2014-03-30 DOI:10.1155/2014/586431
Deepak Kumar Khajuria, Rema Razdan, D Roy Mahapatra
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引用次数: 14

摘要

我们进行了本研究,以探讨心得安(PRO),单独和联合抗吸收剂ZOL,对绝经后骨质疏松大鼠模型的治疗效果。雌性Wistar大鼠在3月龄时进行OVX或假手术。术后12周,将大鼠随机分为6组:(1)sham + vehicle, (2) OVX + vehicle, (3) OVX + ZOL (100 μ g/kg,单次静脉注射),(4)OVX + ZOL (50 μ g/kg,单次静脉注射),(5)OVX + PRO (0.1 mg/kg,每周静脉注射5天),(6)OVX + ZOL (50 μ g/kg,单次静脉注射)+ PRO (0.1 mg/kg,每周静脉注射5天),连续12周。在治疗研究结束时,评估各种骨参数。关于腰椎和股中轴机械强度的改善,ZOL和PRO联合治疗比单独使用每种药物更有效。此外,ZOL和PRO联合治疗对OVX大鼠小梁微结构的保护优于ZOL或PRO单药治疗。这些数据表明,ZOL + PRO联合治疗是骨质疏松症患者的一种潜在有效的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The combination therapy with zoledronic Acid and propranolol improves the trabecular microarchitecture and mechanical property in an rat model of postmenopausal osteoporosis.

We conducted the present study to investigate the therapeutic effects of propranolol (PRO), alone and in combination with the antiresorptive agent ZOL, in a rat model of postmenopausal osteoporosis. Female Wistar rats were OVX or sham-operated at 3 months of age. Twelve weeks after surgery, rats were randomized into six groups: (1) sham + vehicle, (2) OVX + vehicle, (3) OVX + ZOL (100  μ g/kg, i.v. single dose), (4) OVX + ZOL (50  μ g/kg, i.v. single dose), (5) OVX + PRO (0.1 mg/kg, s.c. 5 days per week), and (6) OVX + ZOL (50  μ g/kg, i.v. single dose) + PRO (0.1 mg/kg, s.c. 5 days per week) for 12 weeks. At the end of treatment study, various bone parameters were evaluated. With respect to improvement in the mechanical strength of the lumbar spine and the femoral mid-shaft, the combination treatment of ZOL and PRO was more effective than each drug administered as a monotherapy. Moreover, combination therapy using ZOL and PRO preserved the trabecular microarchitecture better than single-drug therapy using ZOL or PRO in OVX rats. These data suggest that combination therapy with ZOL plus PRO represents a potentially useful therapeutic option for patients with osteoporosis.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
6
审稿时长
20 weeks
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