-
Something wrong with this record ?
The effect of topiramate and lamotrigine on rat bone mass, structure and metabolism
J. Simko, S. Fekete, I. Gradosova, J. Malakova, H. Zivna, M. Valis, V. Palicka, P. Zivny,
Language English Country Netherlands
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Absorptiometry, Photon MeSH
- Alkaline Phosphatase metabolism MeSH
- Anticonvulsants administration & dosage MeSH
- Administration, Oral MeSH
- Biomechanical Phenomena drug effects MeSH
- Enzyme-Linked Immunosorbent Assay MeSH
- Fructose analogs & derivatives pharmacology MeSH
- Collagen Type I metabolism MeSH
- Bone and Bones drug effects metabolism MeSH
- Bone Density drug effects MeSH
- Bone Morphogenetic Protein 2 metabolism MeSH
- Rats MeSH
- Models, Animal MeSH
- Statistics, Nonparametric MeSH
- Orchiectomy MeSH
- Osteoprotegerin blood MeSH
- Peptide Fragments metabolism MeSH
- Peptides metabolism MeSH
- Rats, Wistar MeSH
- Procollagen metabolism MeSH
- Body Composition drug effects MeSH
- Body Weight drug effects MeSH
- Triazines administration & dosage MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't 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.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15008192
- 003
- CZ-PrNML
- 005
- 20150330114417.0
- 007
- ta
- 008
- 150306s2014 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.jns.2014.02.032 $2 doi
- 035 __
- $a (PubMed)24629477
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Simko, Julius $u Department of Neurology, Charles University in Prague, Faculty of Medicine and University Hospital in Hradec Kralove, Czech Republic. Electronic address: simko.julius@gmail.com.
- 245 14
- $a The effect of topiramate and lamotrigine on rat bone mass, structure and metabolism / $c J. Simko, S. Fekete, I. Gradosova, J. Malakova, H. Zivna, M. Valis, V. Palicka, P. Zivny,
- 520 9_
- $a 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.
- 650 _2
- $a absorpční fotometrie $7 D015502
- 650 _2
- $a aplikace orální $7 D000284
- 650 _2
- $a alkalická fosfatasa $x metabolismus $7 D000469
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a antikonvulziva $x aplikace a dávkování $7 D000927
- 650 _2
- $a biomechanika $x účinky léků $7 D001696
- 650 _2
- $a složení těla $x účinky léků $7 D001823
- 650 _2
- $a tělesná hmotnost $x účinky léků $7 D001835
- 650 _2
- $a kostní denzita $x účinky léků $7 D015519
- 650 _2
- $a kostní morfogenetický protein 2 $x metabolismus $7 D055396
- 650 _2
- $a kosti a kostní tkáň $x účinky léků $x metabolismus $7 D001842
- 650 _2
- $a kolagen typu I $x metabolismus $7 D024042
- 650 _2
- $a ELISA $7 D004797
- 650 _2
- $a fruktosa $x analogy a deriváty $x farmakologie $7 D005632
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a modely u zvířat $7 D023421
- 650 _2
- $a orchiektomie $7 D009919
- 650 _2
- $a osteoprotegerin $x krev $7 D053244
- 650 _2
- $a peptidové fragmenty $x metabolismus $7 D010446
- 650 _2
- $a peptidy $x metabolismus $7 D010455
- 650 _2
- $a prokolagen $x metabolismus $7 D011347
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a neparametrická statistika $7 D018709
- 650 _2
- $a triaziny $x aplikace a dávkování $7 D014227
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Fekete, Sona $u Institute of Clinical Biochemistry and Diagnostics, Charles University in Prague, Faculty of Medicine and University Hospital in Hradec Kralove, Czech Republic.
- 700 1_
- $a Gradosova, Iveta $u Institute of Clinical Biochemistry and Diagnostics, Charles University in Prague, Faculty of Medicine and University Hospital in Hradec Kralove, Czech Republic.
- 700 1_
- $a Malakova, Jana $u Institute of Clinical Biochemistry and Diagnostics, Charles University in Prague, Faculty of Medicine and University Hospital in Hradec Kralove, Czech Republic.
- 700 1_
- $a Zivna, Helena $u Radioisotope Laboratories and Vivarium, Charles University in Prague, Faculty of Medicine in Hradec Kralove, Hradec Kralove, Czech Republic.
- 700 1_
- $a Valis, Martin $u Department of Neurology, Charles University in Prague, Faculty of Medicine and University Hospital in Hradec Kralove, Czech Republic.
- 700 1_
- $a Palicka, Vladimir $u Institute of Clinical Biochemistry and Diagnostics, Charles University in Prague, Faculty of Medicine and University Hospital in Hradec Kralove, Czech Republic.
- 700 1_
- $a Zivny, Pavel $u Institute of Clinical Biochemistry and Diagnostics, Charles University in Prague, Faculty of Medicine and University Hospital in Hradec Kralove, Czech Republic.
- 773 0_
- $w MED00003004 $t Journal of the neurological sciences $x 1878-5883 $g Roč. 340, č. 1-2 (2014), s. 80-5
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/24629477 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20150306 $b ABA008
- 991 __
- $a 20150330114646 $b ABA008
- 999 __
- $a ok $b bmc $g 1065465 $s 890992
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2014 $b 340 $c 1-2 $d 80-5 $i 1878-5883 $m Journal of the neurological sciences $n J Neurol Sci $x MED00003004
- LZP __
- $a Pubmed-20150306