特立帕肽和依替卡西肽可改善慢性肾病模型大鼠的骨骼、纤维化和脂肪参数。

Osteoporosis and sarcopenia Pub Date : 2023-12-01 Epub Date: 2023-12-21 DOI:10.1016/j.afos.2023.11.002
Shun Igarashi, Yuji Kasukawa, Koji Nozaka, Hiroyuki Tsuchie, Kazunobu Abe, Hikaru Saito, Ryo Shoji, Fumihito Kasama, Shuntaro Harata, Kento Okamoto, Keita Oya, Naohisa Miyakoshi
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引用次数: 0

摘要

目的:慢性肾脏病(CKD)并发继发性甲状旁腺功能亢进症(SHPT)会增加脆性骨折的风险。依替卡西肽(EC)是一种治疗 SHPT 的药物,可降低血清甲状旁腺激素(PTH)水平。然而,与特立帕肽(TPTD)等骨质疏松症药物联合治疗的效果仍不明确。本研究探讨了EC和TPTD联合治疗对CKD模型大鼠骨骼的影响:方法:用 0.75% 腺嘌呤饮食喂养 8 周大雄性 Wistar 大鼠 4 周,建立 CKD 模型。20 周龄时,将大鼠分为 4 组(每组 9-10 只):CKD组(给药)、TPTD组(30 μg/kg,每周3次)、EC组(0.6 mg/kg,每天)和Comb组(TPTD和EC联合)。EC 组从 20 周龄开始注射,连续 12 周;TPTD 组从 24 周龄开始注射,连续 8 周。治疗后,对以下项目进行了评估:骨矿物质密度、骨强度、生化测试、骨和脂肪组织形态测量以及显微计算机断层扫描:结果:在 CKD 模型大鼠中,EC 和 TPTD 联合治疗对增加皮质骨厚度和骨强度以及抑制孔隙率更有效。此外,联合治疗还能减少骨髓脂肪和纤维化,增加骨量,改善骨小梁的骨微结构:通过观察骨量、骨强度、结构特性和骨髓脂肪含量的改善等益处,联合疗法可能是改善 CKD 患者骨脆性的一种潜在方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Teriparatide and etelcalcetide improve bone, fibrosis, and fat parameters in chronic kidney disease model rats.

Objectives: Chronic kidney disease (CKD) complicated by secondary hyperparathyroidism (SHPT) is associated with an increased risk of fragility fractures. Etelcalcetide (EC) is a treatment for SHPT that reduces serum parathyroid hormone (PTH) levels. However, the effects of combined treatment with osteoporosis drugs such as teriparatide (TPTD) remain unclear. This study investigates the combined effects of EC and TPTD on bone in CKD model rats.

Methods: The CKD model was established in 8-week-old male Wistar rats by feeding them a 0.75% adenine diet for 4 weeks. At 20 weeks of age, the rats were divided into 4 groups (N = 9-10 in each group): CKD group (vehicle administration), TPTD group (30 μg/kg, 3 times/week), EC group (0.6 mg/kg, daily), and Comb group (TPTD and EC combined). EC was injected for 12 weeks starting at 20 weeks of age, and TPTD was injected for 8 weeks starting at 24 weeks of age. After treatment, the followings were evaluated: bone mineral density, bone strength, biochemical tests, bone and fat histomorphometry, and micro-computed tomography.

Results: In CKD model rats, the combination of EC and TPTD was more effective in increasing cortical bone thickness and bone strength and inhibiting porosity. In addition, the combined treatment decreased bone marrow adiposity and fibrosis, and it increased bone mass and improved bone microstructure in trabecular bone.

Conclusions: With the observed benefits such as improved bone mass, bone strength, structural properties, and bone marrow adiposity, combination therapy may be a potential way to improve bone fragility in CKD.

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