Treating osteoporosis by targeting parathyroid hormone to bone

被引:83
作者
Ponnapakkam, T. [1 ,2 ]
Katikaneni, R. [1 ,2 ]
Sakon, J. [3 ]
Stratford, R. [4 ]
Gensure, R. C. [1 ,2 ]
机构
[1] Childrens Hosp Montefiore, Bronx, NY 10467 USA
[2] Albert Einstein Coll Med, Bronx, NY 10467 USA
[3] Univ Arkansas, Fayetteville, AR 72701 USA
[4] Xavier Univ Louisiana, Coll Pharm, New Orleans, LA USA
关键词
CLOSTRIDIUM-HISTOLYTICUM COLLAGENASE; POSTMENOPAUSAL WOMEN; MINERAL DENSITY; BINDING DOMAIN; ALENDRONATE; FRACTURES; PROTEIN; INCREASES; CELLS; TRIAL;
D O I
10.1016/j.drudis.2013.07.015
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Osteoporosis is a major public health problem despite widespread use of bisphosphonate therapy. PTH(1-34) is a more effective treatment; but its use has been limited by side effects (hypercalcemia, tumor risk) and inconvenient dosing (daily injection). Long-acting forms of PTH are also effective but cause severe hypercalcemia, presumably from effects in kidney. We hypothesized that targeted delivery of PTH to bone using a collagen binding domain (PTH-CBD) could reduce hypercalcemia. PTH-CBD is cleared from serum within 12 hours after subcutaneous administration. In ovariectomized rats, monthly administration of PTH-CBD increased spinal BMD by 14.2% with no associated hypercalcemia. Such bone-targeted anabolic agents may ultimately allow the superior efficacy of anabolic therapy to be obtained with the dosing convenience of bisphosphonates.
引用
收藏
页码:204 / 208
页数:5
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