-
Je něco špatně v tomto záznamu ?
Longitudinal study revealing motor, cognitive and behavioral decline in a transgenic minipig model of Huntington's disease
M. Baxa, B. Levinska, M. Skrivankova, M. Pokorny, J. Juhasova, J. Klima, J. Klempir, J. Motlı K, S. Juhas, Z. Ellederova,
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2011
Free Medical Journals
od 2008 do Před 6 měsíci
Freely Accessible Science Journals
od 2008
PubMed Central
od 2008
Europe PubMed Central
od 2008
ProQuest Central
od 2008-01-01
Open Access Digital Library
od 2011-01-01
Health & Medicine (ProQuest)
od 2008-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2008
PubMed
31704691
DOI
10.1242/dmm.041293
Knihovny.cz E-zdroje
- MeSH
- chování zvířat fyziologie MeSH
- geneticky modifikovaná zvířata MeSH
- Huntingtonova nemoc komplikace patofyziologie MeSH
- jazyk MeSH
- kognice fyziologie MeSH
- kondiční příprava zvířat MeSH
- longitudinální studie MeSH
- miniaturní prasata MeSH
- modely nemocí na zvířatech MeSH
- pohybová aktivita * MeSH
- prasata MeSH
- psychický stres komplikace MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Huntington's disease (HD) is an inherited devastating neurodegenerative disease with no known cure to date. Several therapeutic treatments for HD are in development, but their safety, tolerability and efficacy need to be tested before translation to bedside. The monogenetic nature of this disorder has enabled the generation of transgenic animal models carrying a mutant huntingtin (mHTT) gene causing HD. A large animal model reflecting disease progression in humans would be beneficial for testing the potential therapeutic approaches. Progression of the motor, cognitive and behavioral phenotype was monitored in transgenic Huntington's disease minipigs (TgHD) expressing the N-terminal part of human mHTT. New tests were established to investigate physical activity by telemetry, and to explore the stress-induced behavioral and cognitive changes in minipigs. The longitudinal study revealed significant differences between 6- to 8-year-old TgHD animals and their wild-type (WT) controls in a majority of the tests. The telemetric study showed increased physical activity of 4.6- to 6.5-year-old TgHD boars compared to their WT counterparts during the lunch period as well as in the afternoon. Our phenotypic study indicates progression in adult TgHD minipigs and therefore this model could be suitable for longstanding preclinical studies of HD.This article has an associated First Person interview with the first author of the paper.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20023334
- 003
- CZ-PrNML
- 005
- 20201214125800.0
- 007
- ta
- 008
- 201125s2019 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1242/dmm.041293 $2 doi
- 035 __
- $a (PubMed)31704691
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Baxa, Monika $u Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 277 21 Libechov, Czech Republic. Department of Cell Biology, Faculty of Science, Charles University in Prague, 128 00 Prague, Czech Republic.
- 245 10
- $a Longitudinal study revealing motor, cognitive and behavioral decline in a transgenic minipig model of Huntington's disease / $c M. Baxa, B. Levinska, M. Skrivankova, M. Pokorny, J. Juhasova, J. Klima, J. Klempir, J. Motlı K, S. Juhas, Z. Ellederova,
- 520 9_
- $a Huntington's disease (HD) is an inherited devastating neurodegenerative disease with no known cure to date. Several therapeutic treatments for HD are in development, but their safety, tolerability and efficacy need to be tested before translation to bedside. The monogenetic nature of this disorder has enabled the generation of transgenic animal models carrying a mutant huntingtin (mHTT) gene causing HD. A large animal model reflecting disease progression in humans would be beneficial for testing the potential therapeutic approaches. Progression of the motor, cognitive and behavioral phenotype was monitored in transgenic Huntington's disease minipigs (TgHD) expressing the N-terminal part of human mHTT. New tests were established to investigate physical activity by telemetry, and to explore the stress-induced behavioral and cognitive changes in minipigs. The longitudinal study revealed significant differences between 6- to 8-year-old TgHD animals and their wild-type (WT) controls in a majority of the tests. The telemetric study showed increased physical activity of 4.6- to 6.5-year-old TgHD boars compared to their WT counterparts during the lunch period as well as in the afternoon. Our phenotypic study indicates progression in adult TgHD minipigs and therefore this model could be suitable for longstanding preclinical studies of HD.This article has an associated First Person interview with the first author of the paper.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a geneticky modifikovaná zvířata $7 D030801
- 650 _2
- $a chování zvířat $x fyziologie $7 D001522
- 650 _2
- $a kognice $x fyziologie $7 D003071
- 650 _2
- $a modely nemocí na zvířatech $7 D004195
- 650 _2
- $a Huntingtonova nemoc $x komplikace $x patofyziologie $7 D006816
- 650 _2
- $a longitudinální studie $7 D008137
- 650 12
- $a pohybová aktivita $7 D009043
- 650 _2
- $a kondiční příprava zvířat $7 D010805
- 650 _2
- $a psychický stres $x komplikace $7 D013315
- 650 _2
- $a prasata $7 D013552
- 650 _2
- $a miniaturní prasata $7 D013556
- 650 _2
- $a jazyk $7 D014059
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Levinska, Bozena $u Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 277 21 Libechov, Czech Republic. Department of Cell Biology, Faculty of Science, Charles University in Prague, 128 00 Prague, Czech Republic.
- 700 1_
- $a Skrivankova, Monika $u Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 277 21 Libechov, Czech Republic. Department of Cell Biology, Faculty of Science, Charles University in Prague, 128 00 Prague, Czech Republic.
- 700 1_
- $a Pokorny, Matous $u Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 277 21 Libechov, Czech Republic. Department of Circuit Theory, Faculty of Electrical Engineering, Czech Technical University in Prague, 166 27 Prague, Czech Republic.
- 700 1_
- $a Juhasova, Jana $u Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 277 21 Libechov, Czech Republic.
- 700 1_
- $a Klima, Jiri $u Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 277 21 Libechov, Czech Republic.
- 700 1_
- $a Klempir, Jiri $u Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 277 21 Libechov, Czech Republic. Department of Neurology and Centre of Clinical Neuroscience, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, 128 21 Prague, Czech Republic.
- 700 1_
- $a Motlı K, Jan $u Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 277 21 Libechov, Czech Republic.
- 700 1_
- $a Juhas, Stefan $u Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 277 21 Libechov, Czech Republic ellederova@iapg.cas.cz juhas@iapg.cas.cz.
- 700 1_
- $a Ellederova, Zdenka $u Laboratory of Cell Regeneration and Plasticity, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, 277 21 Libechov, Czech Republic ellederova@iapg.cas.cz juhas@iapg.cas.cz.
- 773 0_
- $w MED00173721 $t Disease models & mechanisms $x 1754-8411 $g Roč. 13, č. 2 (2019)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31704691 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20201125 $b ABA008
- 991 __
- $a 20201214125759 $b ABA008
- 999 __
- $a ok $b bmc $g 1595653 $s 1114010
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 13 $c 2 $e 20191212 $i 1754-8411 $m Disease models & mechanisms $n Dis Model Mech $x MED00173721
- LZP __
- $a Pubmed-20201125