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Anticancer Drugs. 2014 Jan;25(1):30-8. doi: 10.1097/CAD.0b013e3283650bff.

本文引用的文献

1
Treatment for chemotherapy-induced alopecia in mice using parathyroid hormone agonists and antagonists linked to a collagen binding domain.用与胶原蛋白结合域相连的甲状旁腺激素激动剂和拮抗剂治疗小鼠的化疗引起的脱发。
Int J Cancer. 2012 Sep 1;131(5):E813-21. doi: 10.1002/ijc.27379. Epub 2012 Jan 24.
2
Prevention of chemotherapy-induced osteoporosis by cyclophosphamide with a long-acting form of parathyroid hormone.用甲状旁腺激素长效形式的环磷酰胺预防化疗引起的骨质疏松症。
J Endocrinol Invest. 2011 Dec;34(11):e392-7. doi: 10.3275/7864. Epub 2011 Jul 12.
3
Monthly administration of a novel PTH-collagen binding domain fusion protein is anabolic in mice.新型甲状旁腺激素-胶原蛋白结合域融合蛋白每月给药可促进小鼠的合成代谢。
Calcif Tissue Int. 2011 Jun;88(6):511-20. doi: 10.1007/s00223-011-9485-1. Epub 2011 Apr 22.
4
Disruption of PTH receptor 1 in T cells protects against PTH-induced bone loss.破骨细胞 PTH 受体 1 可预防 PTH 诱导的骨丢失。
PLoS One. 2010 Aug 20;5(8):e12290. doi: 10.1371/journal.pone.0012290.
5
Parathyroid hormone and bone healing.甲状旁腺激素与骨愈合。
Calcif Tissue Int. 2010 Jul;87(1):1-13. doi: 10.1007/s00223-010-9360-5. Epub 2010 Apr 29.
6
A new technique for precisely and accurately measuring lumbar spine bone mineral density in mice using clinical dual energy X-ray absorptiometry (DXA).一种使用临床双能 X 射线吸收法(DXA)精确、准确测量小鼠腰椎骨密度的新技术。
Toxicol Mech Methods. 2009 Mar;19(3):225-31. doi: 10.1080/15376510802499030.
7
Of mice and men: divergent risks of teriparatide-induced osteosarcoma.老鼠与人:特立帕肽致骨肉瘤的风险差异。
Osteoporos Int. 2010 Jun;21(6):1041-5. doi: 10.1007/s00198-009-1004-0. Epub 2009 Jul 14.
8
Hip fracture protection by alendronate treatment in postmenopausal women with osteoporosis: a review of the literature.阿仑膦酸盐治疗对绝经后骨质疏松症女性的髋部骨折保护作用:文献综述
Clin Interv Aging. 2008;3(3):483-9. doi: 10.2147/cia.s3177.
9
Mechanisms of anabolic therapies for osteoporosis.骨质疏松症的合成代谢治疗机制。
N Engl J Med. 2007 Aug 30;357(9):905-16. doi: 10.1056/NEJMra067395.
10
Infrequent delivery of a long-acting PTH-Fc fusion protein has potent anabolic effects on cortical and cancellous bone.长效甲状旁腺激素-Fc融合蛋白的间歇性给药对皮质骨和松质骨具有强大的合成代谢作用。
J Bone Miner Res. 2007 Oct;22(10):1534-47. doi: 10.1359/jbmr.070616.

单次注射合成代谢性骨制剂,甲状旁腺激素-胶原结合域(PTH-CBD),可使正常雌性小鼠的骨密度持续增加长达 12 个月。

A single injection of the anabolic bone agent, parathyroid hormone-collagen binding domain (PTH-CBD), results in sustained increases in bone mineral density for up to 12 months in normal female mice.

机构信息

Department of Pediatric Endocrinology, Children's Hospital at Montefiore and Albert Einstein College of Medicine, Bronx, NY, USA.

出版信息

Calcif Tissue Int. 2012 Sep;91(3):196-203. doi: 10.1007/s00223-012-9626-1. Epub 2012 Jul 18.

DOI:10.1007/s00223-012-9626-1
PMID:22806683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3693552/
Abstract

Parathyroid hormone (PTH) is the most effective osteoporosis treatment, but it is only effective if administered by daily injections. We fused PTH(1-33) to a collagen binding domain (PTH-CBD) to extend its activity, and have shown an anabolic bone effect with monthly dosing. We tested the duration of action of this compound with different routes of administration. Normal young C57BL/6J mice received a single intraperitoneal injection of PTH-CBD (320 μg/kg). PTH-CBD treated mice showed a 22.2 % increase in bone mineral density (BMD) at 6 months and 12.8 % increase at 12 months. When administered by subcutaneous injection, PTH-CBD again caused increases in BMD, 15.2 % at 6 months and 14.3 % at 12 months. Radiolabeled PTH-CBD was concentrated in bone and skin after either route of administration. We further investigated skin effects of PTH-CBD, and histological analysis revealed an apparent increase in anagen VI hair follicles. A single dose of PTH-CBD caused sustained increases in BMD by >10 % for 1 year in normal mice, regardless of the route of administration, thus showing promise as a potential osteoporosis therapy.

摘要

甲状旁腺激素(PTH)是最有效的骨质疏松症治疗方法,但只有通过每日注射才能有效。我们将 PTH(1-33)融合到胶原结合结构域(PTH-CBD)中以延长其活性,并通过每月给药显示出合成代谢的骨效应。我们用不同的给药途径测试了这种化合物的作用持续时间。正常的年轻 C57BL/6J 小鼠接受了单次腹腔内注射 PTH-CBD(320μg/kg)。PTH-CBD 处理的小鼠在 6 个月时骨矿物质密度(BMD)增加了 22.2%,12 个月时增加了 12.8%。当通过皮下注射给药时,PTH-CBD 再次引起 BMD 增加,6 个月时增加 15.2%,12 个月时增加 14.3%。两种给药途径后,放射性标记的 PTH-CBD 均集中在骨和皮肤中。我们进一步研究了 PTH-CBD 的皮肤作用,组织学分析显示生长期 VI 毛囊明显增加。单次给予 PTH-CBD 可使正常小鼠的 BMD 持续增加>10%,持续 1 年,无论给药途径如何,因此有望成为一种潜在的骨质疏松症治疗方法。