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人甲状旁腺激素(1-34)可加速食蟹猴股骨截骨模型中的自然骨折愈合过程。

Human parathyroid hormone (1-34) accelerates natural fracture healing process in the femoral osteotomy model of cynomolgus monkeys.

作者信息

Manabe Takeshi, Mori Satoshi, Mashiba Tasuku, Kaji Yoshio, Iwata Ken, Komatsubara Satoshi, Seki Azusa, Sun Yong-Xin, Yamamoto Tetsuji

机构信息

Department of Orthopedic Surgery, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa, Japan.

出版信息

Bone. 2007 Jun;40(6):1475-82. doi: 10.1016/j.bone.2007.01.015. Epub 2007 Feb 2.

Abstract

Several studies in rats have demonstrated that parathyroid hormone accelerates fracture healing by increasing callus formation or stimulating callus remodeling. However the effect of PTH on fracture healing has not been tested using large animals with Haversian remodeling system. Using cynomolgus monkey that has intracortical remodeling similar to humans, we examined whether intermittent treatment with human parathyroid hormone [hPTH(1-34)] accelerates the fracture healing process, especially callus remodeling, and restores geometrical shapes and mechanical properties of osteotomized bone. Seventeen female cynomolgus monkeys aged 18-19 years were allocated into three groups: control (CNT, n=6), low-dose PTH (0.75 microg/kg; PTH-L, n=6), and high-dose PTH (7.5 microg/kg; PTH-H, n=5) groups. In all animals, twice a week subcutaneous injection was given for 3 weeks. Then fracture was produced surgically by transversely cutting the midshaft of the right femur and fixing with stainless plate. After fracture, intermittent PTH treatment was continued until sacrifice at 26 weeks after surgery. The femora were assessed by soft X-ray, three-point bending mechanical test, histomorphometry, and degree of mineralization in bone (DMB) measurement. Soft X-ray showed that complete bone union occurred in all groups, regardless of treatment. Ultimate stress and elastic modulus in fractured femur were significantly higher in PTH-H than in CNT. Total area and percent bone area of the femur were significantly lower in both PTH-L and PTH-H than in CNT. Callus porosity decreased dose-dependently following PTH treatment. Mean DMB of callus was significantly higher in PTH-H than in CNT or PTH-L. These results suggested that PTH decreased callus size and accelerated callus maturation in the fractured femora. PTH accelerates the natural fracture healing process by shrinking callus size and increasing degree of mineralization of the fracture callus, thereby restoring intrinsic material properties of osteotomized femur shaft in cynomolgus monkeys although there were no significant differences among the groups for structural parameters.

摘要

多项针对大鼠的研究表明,甲状旁腺激素可通过增加骨痂形成或刺激骨痂重塑来加速骨折愈合。然而,尚未使用具有哈弗斯系统重塑的大型动物来测试甲状旁腺激素对骨折愈合的影响。我们利用食蟹猴(其皮质内重塑与人类相似),研究了人甲状旁腺激素[hPTH(1-34)]的间歇性治疗是否能加速骨折愈合过程,尤其是骨痂重塑,并恢复截骨骨的几何形状和力学性能。17只18 - 19岁的雌性食蟹猴被分为三组:对照组(CNT,n = 6)、低剂量甲状旁腺激素组(0.75微克/千克;PTH-L,n = 6)和高剂量甲状旁腺激素组(7.5微克/千克;PTH-H,n = 5)。对所有动物每周皮下注射两次,持续3周。然后通过横向切断右股骨中段并使用不锈钢板固定进行手术造骨折。骨折后,间歇性甲状旁腺激素治疗持续至术后26周处死。通过软X射线、三点弯曲力学测试、组织形态计量学和骨矿化程度(DMB)测量对股骨进行评估。软X射线显示,无论治疗如何,所有组均实现了完全骨愈合。PTH-H组骨折股骨的极限应力和弹性模量显著高于CNT组。PTH-L组和PTH-H组股骨的总面积和骨面积百分比均显著低于CNT组。甲状旁腺激素治疗后骨痂孔隙率呈剂量依赖性降低。PTH-H组骨痂的平均DMB显著高于CNT组或PTH-L组。这些结果表明,甲状旁腺激素可减小骨折股骨的骨痂大小并加速骨痂成熟。甲状旁腺激素通过缩小骨痂大小和增加骨折骨痂的矿化程度来加速自然骨折愈合过程,从而恢复食蟹猴截骨股骨干的固有材料特性,尽管各组之间的结构参数没有显著差异。

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