首页 | 本学科首页   官方微博 | 高级检索  
     


The effect of gabapentin and pregabalin on bone turnover and bone strength: A prospective study in Wistar rats
Authors:Julius Simko  Iva Karesova  Jan Kremlacek  Zimcikova Eva  Jiri Horacek  Sona Fekete  Jana Malakova  Helena Zivna  Vladimir Palicka
Affiliation:1. Department of Neurology, Charles University, Faculty of Medicine and University Hospital, Hradec Kralove, Czech Republic;2. Institute of Clinical Biochemistry and Diagnostics, Charles University, Faculty of Medicine and University Hospital, Hradec Kralove, Czech Republic;3. Department of Pathophysiology, Charles University, Faculty of Medicine, Hradec Kralove, Czech Republic;4. Department of Social and Clinical Pharmacy, Faculty of Pharmacy in Hradec Kralove, Charles University, Prague, Czech Republic;5. Department of Internal Medicine – Hematology, Charles University, Faculty of Medicine and University Hospital, Hradec Kralove, Czech Republic;6. Radioisotope Laboratories and Vivarium, Charles University, Faculty of Medicine and University Hospital, Hradec Kralove, Czech Republic
Abstract:BackgroundThere are limited data on the effects of GBP on bone and no data for PGB. Some data suggest that there is a significant influence of sex hormone balance on the susceptibility of bone to antiepileptic drug-induced bone loss.MethodsForty-eight male Wistar rats were divided into six groups that were subjected to two surgeries, sham (noORX) or real orchidectomy (ORX), and were fed three diets, a SLD, a SLD enriched with GBP or a SLD enriched with PGB. Dual energy X-ray absorptiometry was used to measure the bone mineral density. The concentrations of bone turnover markers were assayed. The femurs were biomechanically tested.ResultsSignificant reductions in bone mineral density, weight and biomechanical strength were observed in ORX animals. GBP or PGB exposure did not cause significant alterations in bone mineral density or biomechanical strength. No changes in bone turnover markers were observed, except for RANKL. A significant increase was found in the ORX GBP and ORX PGB groups. Within the orchidectomized animal group, RANKL levels were significantly higher in the ORX PGB group than in the ORX GBP group.ConclusionsBecause neither GBP nor PGB affected bone mineral density or mechanical bone strength, both of these antiepileptic drugs could be considered drugs with lower risks to bone health. A shift in RANKL levels indicates that the effects of GBP and PGB on osteoclast activity may be dependent on the hormonal status of animals.
Keywords:Corresponding author.  AEDs  antiepileptic drugs  BALP  bone alkaline phosphatase  BMD  bone mineral density  BTM  bone turnover markers  DEXA  dual energy X-ray absorptiometry  EIAEDs  enzyme-inducing AEDs  GBP  gabapentin  LEV  levetiracetam  LTG  lamotrigine  noORX  gonadally intact  OPG  osteoprotegerin  ORX  orchidectomized  PGB  pregabalin  PINP  amino-terminal propeptide of procollagen type I  PHT  phenytoin  RANKL  receptor activator of nuclear factor-kappa B ligand  SLD  standard laboratory diet  SCL  sclerostin  TPM  topiramate  VPA  valproate  Bone mineral density  Receptor activator of nuclear factor-kappa B ligand  Amino-terminal propeptide of procollagen type I  Bone alkaline phosphatase
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号