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阿巴洛肽(一种甲状旁腺激素1型受体的选择性肽激活剂)治疗一年可增加去卵巢大鼠的骨量和骨强度。

One year of abaloparatide, a selective peptide activator of the PTH1 receptor, increased bone mass and strength in ovariectomized rats.

作者信息

Varela Aurore, Chouinard Luc, Lesage Elisabeth, Guldberg Robert, Smith Susan Y, Kostenuik Paul J, Hattersley Gary

机构信息

Charles River Laboratories, Montreal, Canada.

Petit Institute for Bioengineering, Bioscience and Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.

出版信息

Bone. 2017 Feb;95:143-150. doi: 10.1016/j.bone.2016.11.027. Epub 2016 Nov 25.

Abstract

Abaloparatide is a novel 34 amino acid peptide selected to be a potent and selective activator of the parathyroid hormone receptor 1 (PTHR1) signaling pathway. The effects of 12months of abaloparatide treatment on bone mass, bone strength and bone quality was assessed in osteopenic ovariectomized (OVX) rats. SD rats were subjected to OVX or sham surgery at 6months of age and left untreated for 3months to allow OVX-induced bone loss. Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months. Sham controls (n=18) received vehicle daily. Bone changes were assessed by DXA and pQCT after 0, 3, 6 or 12months of treatment, and destructive biomechanical testing was conducted at month 12 to assess bone strength and bone quality. Abaloparatide dose-dependently increased bone mass at the lumbar spine and at the proximal and diaphyseal regions of the tibia and femur. pQCT revealed that increased cortical bone volume at the tibia was a result of periosteal expansion and endocortical bone apposition. Abaloparatide dose-dependently increased structural strength of L4-L5 vertebral bodies, the femur diaphysis, and the femur neck. Increments in peak load for lumbar spine and the femur diaphysis of abaloparatide-treated rats persisted even after adjusting for treatment-related increments in BMC, and estimated material properties were maintained or increased at the femur diaphysis with abaloparatide. The abaloparatide groups also exhibited significant and positive correlations between bone mass and bone strength at these sites. These data indicate that gains in cortical and trabecular bone mass with abaloparatide are accompanied by and correlated with improvements in bone strength, resulting in maintenance or improvement in bone quality. Thus, this study demonstrated that long-term daily administration of abaloparatide to osteopenic OVX rats led to dose-dependent improvements in bone mass, geometry and strength.

摘要

阿巴洛肽是一种新型的由34个氨基酸组成的肽,被选定为甲状旁腺激素受体1(PTHR1)信号通路的强效和选择性激活剂。在骨质疏松性卵巢切除(OVX)大鼠中评估了12个月阿巴洛肽治疗对骨量、骨强度和骨质量的影响。SD大鼠在6月龄时接受卵巢切除术或假手术,并在3个月内不进行治疗,以使卵巢切除引起骨丢失。在这个骨量减少期后,处死18只OVX大鼠,其余的OVX大鼠每天皮下注射赋形剂(n = 18)或1、5或25μg/kg/d的阿巴洛肽(每个剂量水平n = 18),持续12个月。假手术对照组(n = 18)每天接受赋形剂注射。在治疗0、3、6或12个月后,通过双能X线吸收法(DXA)和外周定量计算机断层扫描(pQCT)评估骨变化,并在第12个月进行破坏性生物力学测试以评估骨强度和骨质量。阿巴洛肽剂量依赖性地增加了腰椎以及胫骨和股骨近端和骨干区域的骨量。pQCT显示,胫骨皮质骨体积增加是骨膜扩张和骨内膜骨附着的结果。阿巴洛肽剂量依赖性地增加了L4-L5椎体、股骨干和股骨颈的结构强度。即使在调整了与治疗相关的骨矿含量(BMC)增加后,阿巴洛肽治疗的大鼠腰椎和股骨干的峰值负荷增加仍然持续,并且阿巴洛肽使股骨干的估计材料特性保持不变或增加。阿巴洛肽组在这些部位的骨量和骨强度之间也表现出显著的正相关。这些数据表明,阿巴洛肽增加皮质骨和小梁骨量的同时伴随着骨强度的改善,并与之相关,从而导致骨质量维持或改善。因此,本研究表明,对骨质疏松性OVX大鼠长期每日给予阿巴洛肽可导致骨量、几何形状和强度的剂量依赖性改善。

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