Intermittent administration of teriparatide enhances graft bone healing and accelerates spinal fusion in rats with glucocorticoid-induced osteoporosis

被引:41
作者
Sugiura, Tsuyoshi [1 ]
Kashii, Masafumi [1 ]
Matsuo, Yohei [1 ]
Morimoto, Tokimitsu [1 ]
Honda, Hirotsugu [1 ]
Kaito, Takashi [1 ]
Iwasaki, Motoki [1 ]
Yoshikawa, Hideki [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Fac Med, Dept Orthoped Surg, Suita, Osaka 5650871, Japan
关键词
Teriparatide; Glucocorticoid-induced osteoporosis; Bone graft; Bone remodeling; Spinal fusion; Adjacent vertebrae; PARATHYROID-HORMONE; 1-34; POSTMENOPAUSAL WOMEN; LUMBAR FUSION; FRACTURE; OSTEOBLASTS; PREVENTION; APOPTOSIS; THERAPY; UPDATE; MICROARCHITECTURE;
D O I
10.1016/j.spinee.2014.08.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
BACKGROUND CONTEXT: There has been no study regarding the effect of intermittent administration of teriparatide (TPTD [recombinant human parathyroid hormone (1-34)]) on spinal fusion in patients with glucocorticoid-induced osteoporosis (GIOP). PURPOSE: To elucidate the effect of intermittent administration of TPTD on spinal fusion in rats with GIOP. STUDY DESIGN: An experimental animal study of rats under continuous glucocorticoid (GC) exposure undergoing spinal fusion surgery and administration of TPTD or saline. METHODS: Male 8-week-old rats (n=18) were administered 5 mg/kg methylprednisolone (MP) for 12 weeks. After 6 weeks of MP administration, the rats underwent posterolateral spinal fusion (L4-L5) with iliac crest autograft. Then, five times a week, they were given either saline or 40 mu g/kg TPTD for 6 weeks. The following assessments were performed: time-course bone microstructural analysis of the fusion mass and adjacent vertebrae (L6), with in vivo microcomputed tomography (mu CT); fusion assessment, with manual palpation testing and three-dimensional CT images; and bone histomorphometrical analysis of the fusion mass. RESULTS: In the TPTD group, values for bone volume and other bone microstructural parameters at the fusion mass increased and peaked 4 weeks after surgery, and these values were significantly greater than those for the control (CNT) group at 4 and 6 weeks after surgery. Fusion assessment showed that fusion rate was higher in the TPTD group than in the CNT group (CNT group: 56%, TPTD group: 89%). Bone histomorphometry revealed that values for bone formation parameters were significantly higher in the TPTD group than in the CNT group. CONCLUSIONS: Under continuous GC exposure in a rat model of spinal fusion, intermittent TPTD administration accelerated bone modeling and remodeling predominantly by stimulating bone formation at the fusion mass and increasing the fusion rate. Intermittent TPTD administration also improved bone microarchitecture of adjacent vertebrae. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:298 / 306
页数:9
相关论文
共 41 条
[1]
Enhancement of graft bone healing by intermittent administration of human parathyroid hormone (1-34) in a rat spinal arthrodesis model [J].
Abe, Yuichiro ;
Takahata, Masahiko ;
Ito, Manabu ;
Irie, Kazuharu ;
Abumi, Kunlyoshi ;
Minami, Akio .
BONE, 2007, 41 (05) :775-785
[2]
Update on Bone Anabolics in Osteoporosis Treatment: Rationale, Current Status, and Perspectives [J].
Baron, Roland ;
Hesse, Eric .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2012, 97 (02) :311-325
[3]
Parathyroid hormone-related protein analog R8-66271 is an effective therapy for impaired bone healing in rabbits on corticosteroid therapy [J].
Bostrom, MPG ;
Gamradt, SC ;
Asnis, P ;
Vickery, BH ;
Hill, E ;
Avnur, Z ;
Waters, RV .
BONE, 2000, 26 (05) :437-442
[4]
THE ROLE OF FUSION AND INSTRUMENTATION IN THE TREATMENT OF DEGENERATIVE SPONDYLOLISTHESIS WITH SPINAL STENOSIS [J].
BRIDWELL, KH ;
SEDGEWICK, TA ;
OBRIEN, MF ;
LENKE, LG ;
BALDUS, C .
JOURNAL OF SPINAL DISORDERS, 1993, 6 (06) :461-472
[5]
Glucocorticoid-induced osteoporosis: an update on current pharmacotherapy and future directions [J].
Bultink, Irene E. M. ;
Baden, Marijke ;
Lems, Willem F. .
EXPERT OPINION ON PHARMACOTHERAPY, 2013, 14 (02) :185-197
[6]
Comparison of trabecular bone microarchitecture and remodeling in glucocorticoid-induced and postmenopausal osteoporosis [J].
Carbonare, LD ;
Arlot, ME ;
Chavassieux, PM ;
Roux, JP ;
Portero, NR ;
Meunier, PJ .
JOURNAL OF BONE AND MINERAL RESEARCH, 2001, 16 (01) :97-103
[7]
Teriparatide increases the maturation of circulating osteoblast precursors [J].
D'Amelio, P. ;
Tamone, C. ;
Sassi, F. ;
D'Amico, L. ;
Roato, I. ;
Patane, S. ;
Ravazzoli, M. ;
Veneziano, L. ;
Ferracini, R. ;
Pescarmona, G. P. ;
Isaia, G. C. .
OSTEOPOROSIS INTERNATIONAL, 2012, 23 (04) :1245-1253
[8]
Osteoporotic fracture and parathyroid hormone [J].
Datta, Nabanita S. .
WORLD JOURNAL OF ORTHOPEDICS, 2011, 2 (08) :67-74
[9]
Standardized Nomenclature, Symbols, and Units for Bone Histomorphometry: A 2012 Update of the Report of the ASBMR Histomorphometry Nomenclature Committee [J].
Dempster, David W. ;
Compston, Juliet E. ;
Drezner, Marc K. ;
Glorieux, Francis H. ;
Kanis, John A. ;
Malluche, Hartmut ;
Meunier, Pierre J. ;
Ott, Susan M. ;
Recker, Robert R. ;
Parfitt, A. Michael .
JOURNAL OF BONE AND MINERAL RESEARCH, 2013, 28 (01) :1-16
[10]
ANABOLIC ACTIONS OF PARATHYROID-HORMONE ON BONE [J].
DEMPSTER, DW ;
COSMAN, F ;
PARISIEN, M ;
SHEN, V ;
LINDSAY, R .
ENDOCRINE REVIEWS, 1993, 14 (06) :690-709