The effect of topiramate and lamotrigine on rat bone mass, structure and metabolism
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24629477
DOI
10.1016/j.jns.2014.02.032
PII: S0022-510X(14)00137-3
Knihovny.cz E-zdroje
- Klíčová slova
- Antiepileptic drugs, Bone markers, Bone mineral density, Lamotrigine, Topiramate,
- MeSH
- absorpční fotometrie MeSH
- alkalická fosfatasa metabolismus MeSH
- antikonvulziva aplikace a dávkování MeSH
- aplikace orální MeSH
- biomechanika účinky léků MeSH
- ELISA MeSH
- fruktosa analogy a deriváty farmakologie MeSH
- kolagen typu I metabolismus MeSH
- kosti a kostní tkáň účinky léků metabolismus MeSH
- kostní denzita účinky léků MeSH
- kostní morfogenetický protein 2 metabolismus MeSH
- krysa rodu Rattus MeSH
- lamotrigin MeSH
- modely u zvířat MeSH
- neparametrická statistika MeSH
- orchiektomie MeSH
- osteoprotegerin krev MeSH
- peptidové fragmenty metabolismus MeSH
- peptidy metabolismus MeSH
- potkani Wistar MeSH
- prokolagen metabolismus MeSH
- složení těla účinky léků MeSH
- tělesná hmotnost účinky léků MeSH
- topiramat MeSH
- triaziny aplikace a dávkování MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- alkalická fosfatasa MeSH
- antikonvulziva MeSH
- collagen type I trimeric cross-linked peptide MeSH Prohlížeč
- fruktosa MeSH
- kolagen typu I MeSH
- kostní morfogenetický protein 2 MeSH
- lamotrigin MeSH
- osteoprotegerin MeSH
- peptidové fragmenty MeSH
- peptidy MeSH
- procollagen Type I N-terminal peptide MeSH Prohlížeč
- prokolagen MeSH
- topiramat MeSH
- triaziny MeSH
There is only limited data concerning the effect of the newer antiepileptic drugs on bone. The objective of this study was to determine the effect of topiramate (TPM) and lamotrigine (LTG) monotherapy on bone mineral density (BMD), mineral content (BMC), bone markers, body composition and bone mechanical strength in the orchidectomized (ORX) rat model. 24 orchidectomized Wistar rats were divided into control and test groups, 8 rats in each group. The control rats received standard laboratory diet (SLD) while rats in the test group were fed with SLD enriched with LTG or TPM for 12 weeks. Dual energy X-ray absorptiometry was used to measure bone mineral density. The concentrations of bone metabolism markers were assayed in bone homogenate. In addition, both femurs were measured and used for biomechanical testing. Compared to the control group, both test groups had significantly lower weight, fat mass, whole body and femur BMD, BMC and reduced mechanical strength of bone. All of these changes were more pronounced in rats exposed to LTG. In conclusion, both LTG and TPM significantly reduce BMD and body weight and impair mechanical strength of bone. A question arises as to the degree of dependence of the effect on the dose. Further studies are warranted to establish whether LTG and TPM may have a clinically significant effect on BMD exclusively in the model of gonadectomized rats, or whether the effect applies also in the model of gonadally intact animals, and in the respective human models.
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