-
Je něco špatně v tomto záznamu ?
Selective impairment of timing in a NMDA hypofunction animal model of psychosis
K. Maleninska, P. Jandourkova, H. Brozka, A. Stuchlik, T. Nekovarova
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- antagonisté excitačních aminokyselin aplikace a dávkování farmakologie MeSH
- bludiště - učení účinky léků MeSH
- chování zvířat účinky léků MeSH
- dizocilpinmaleát aplikace a dávkování farmakologie MeSH
- kognitivní dysfunkce chemicky indukované patofyziologie MeSH
- krysa rodu rattus MeSH
- modely nemocí na zvířatech MeSH
- potkani Long-Evans MeSH
- schizofrenie chemicky indukované MeSH
- učení vyhýbat se účinky léků MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Schizophrenia is severe neuropsychiatric disease, which is commonly accompanied not only by positive or negative symptoms, but also by cognitive impairment. To study neuronal mechanisms underlying cognitive distortions and mechanisms underlying schizophrenia, animal pharmacological models of cognitive symptoms are commonly used. Between various cognitive impairments in schizophrenia patients, disturbed time perception has often been reported. Here, we examined temporal and spatial cognition in a modified Carousel maze task in the animal model of schizophrenia induced by non-competitive NMDA-receptor antagonists MK-801. Male Long-Evans rats (n = 18) first learned to avoid the aversive sector on a rotating arena in both dark and light intervals. We verified that during dark, rats used temporal cues, while during light they relied predominantly on spatial cues. We demonstrated that the timing strategy depends on the stable rotation speed of the arena and on the repositioning clues such as aversive stimuli. During testing (both in light and dark intervals), half of the rats received MK-801 and the control half received saline solution. We observed dose-dependent disruptions of both temporal and spatial cognition. Namely, both doses of MK-801 (0.1 and 0.12 mg/kg) significantly impaired timing strategy in the dark and increased locomotor activity. MK-801 dose 0.1 mg/kg, but not 0.12, also impaired spatial avoidance strategy in light. We found that the timing strategy is more sensitive to NMDA antagonist MK-801 than the spatial strategy. To conclude, a modified version of the Carousel maze is a useful and sensitive tool for detecting timing impairments in the MK-801 induced rodent model of schizophrenia.
Department of Zoology Faculty of Science Charles University Albertov 6 12800 Prague 2 Czech Republic
National Institute of Mental Health Topolova 748 25067 Klecany Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22010992
- 003
- CZ-PrNML
- 005
- 20220506125808.0
- 007
- ta
- 008
- 220425s2022 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.bbr.2021.113671 $2 doi
- 035 __
- $a (PubMed)34788697
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Maleninska, Kristyna $u Laboratory of Neurophysiology of Memory, Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic; National Institute of Mental Health, Topolova 748, 25067 Klecany, Czech Republic; Department of Physiology, Faculty of Science, Charles University, Albertov 6, 12800 Prague 2, Czech Republic. Electronic address: kristyna.maleninska@fgu.cas.cz
- 245 10
- $a Selective impairment of timing in a NMDA hypofunction animal model of psychosis / $c K. Maleninska, P. Jandourkova, H. Brozka, A. Stuchlik, T. Nekovarova
- 520 9_
- $a Schizophrenia is severe neuropsychiatric disease, which is commonly accompanied not only by positive or negative symptoms, but also by cognitive impairment. To study neuronal mechanisms underlying cognitive distortions and mechanisms underlying schizophrenia, animal pharmacological models of cognitive symptoms are commonly used. Between various cognitive impairments in schizophrenia patients, disturbed time perception has often been reported. Here, we examined temporal and spatial cognition in a modified Carousel maze task in the animal model of schizophrenia induced by non-competitive NMDA-receptor antagonists MK-801. Male Long-Evans rats (n = 18) first learned to avoid the aversive sector on a rotating arena in both dark and light intervals. We verified that during dark, rats used temporal cues, while during light they relied predominantly on spatial cues. We demonstrated that the timing strategy depends on the stable rotation speed of the arena and on the repositioning clues such as aversive stimuli. During testing (both in light and dark intervals), half of the rats received MK-801 and the control half received saline solution. We observed dose-dependent disruptions of both temporal and spatial cognition. Namely, both doses of MK-801 (0.1 and 0.12 mg/kg) significantly impaired timing strategy in the dark and increased locomotor activity. MK-801 dose 0.1 mg/kg, but not 0.12, also impaired spatial avoidance strategy in light. We found that the timing strategy is more sensitive to NMDA antagonist MK-801 than the spatial strategy. To conclude, a modified version of the Carousel maze is a useful and sensitive tool for detecting timing impairments in the MK-801 induced rodent model of schizophrenia.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a učení vyhýbat se $x účinky léků $7 D001362
- 650 _2
- $a chování zvířat $x účinky léků $7 D001522
- 650 _2
- $a kognitivní dysfunkce $x chemicky indukované $x patofyziologie $7 D060825
- 650 _2
- $a modely nemocí na zvířatech $7 D004195
- 650 _2
- $a dizocilpinmaleát $x aplikace a dávkování $x farmakologie $7 D016291
- 650 _2
- $a antagonisté excitačních aminokyselin $x aplikace a dávkování $x farmakologie $7 D018691
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a bludiště - učení $x účinky léků $7 D018782
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Long-Evans $7 D020318
- 650 _2
- $a schizofrenie $x chemicky indukované $7 D012559
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Jandourkova, Pavla $u Laboratory of Neurophysiology of Memory, Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic; Department of Physiology, Faculty of Science, Charles University, Albertov 6, 12800 Prague 2, Czech Republic
- 700 1_
- $a Brozka, Hana $u Laboratory of Neurophysiology of Memory, Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic
- 700 1_
- $a Stuchlik, Ales $u Laboratory of Neurophysiology of Memory, Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic. Electronic address: ales.stuchlik@fgu.cas.cz
- 700 1_
- $a Nekovarova, Tereza $u Laboratory of Neurophysiology of Memory, Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic; National Institute of Mental Health, Topolova 748, 25067 Klecany, Czech Republic; Department of Zoology, Faculty of Science, Charles University, Albertov 6, 12800 Prague 2, Czech Republic. Electronic address: tereza.nekovarova@nudz.cz
- 773 0_
- $w MED00000660 $t Behavioural brain research $x 1872-7549 $g Roč. 419, č. - (2022), s. 113671
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/34788697 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20220425 $b ABA008
- 991 __
- $a 20220506125801 $b ABA008
- 999 __
- $a ok $b bmc $g 1788884 $s 1162190
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2022 $b 419 $c - $d 113671 $e 20211114 $i 1872-7549 $m Behavioural brain research $n Behav Brain Res $x MED00000660
- LZP __
- $a Pubmed-20220425