-
Something wrong with this record ?
Nicotine and kainic acid effects on cortical epileptic afterdischarges in immature rats
V. Riljak, D. Marešová, K. Jandová, J. Pokorný
Language English Country Czech Republic
Document type Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
NLK
Directory of Open Access Journals
from 1991
Free Medical Journals
from 1998
ProQuest Central
from 2005-01-01
Medline Complete (EBSCOhost)
from 2006-01-01
Nursing & Allied Health Database (ProQuest)
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 1998
- MeSH
- Action Potentials drug effects MeSH
- Epilepsy chemically induced physiopathology prevention & control MeSH
- Rats MeSH
- Kainic Acid * MeSH
- Drug Interactions MeSH
- Cerebral Cortex drug effects physiopathology MeSH
- Nicotine administration & dosage MeSH
- Animals, Newborn MeSH
- Rats, Wistar MeSH
- Treatment Outcome MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
Aim of the study was to test the effect of nicotine (NIC) and kainic acid (KA) co-treatment in immature rats. Male Wistar albino rats (two different age groups) were chosen for the study. Experiments started on postnatal day (PD) 8 or 21 and animals were treated twice a day for three days with nicotine, fourth day KA was administered. Animals at PD12 (PD25 respectively) were examined electrophysiologically for cortical epileptic afterdischarges (ADs). First cortical ADs in PD12 animals were longer, when compared to PD25 rats (group treated with both substances). Nor NIC or KA treatment affected the length of discharges in PD12 rats. Older experimental group exhibited the shortening of the first ADs (group treated with NIC and KA, compared with groups exposed to single treatment). Few changes were found in KA treated group - 2(nd) and 4(th) ADs were shorter when compared with first ADs. These results demonstrate that NIC treatment played minor role in seizure susceptibility of PD12 rats, sensitivity to NIC differs during ontogenesis and subconvulsive dose of KA influenced the length of discharges only in PD25 animals.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13033342
- 003
- CZ-PrNML
- 005
- 20131025121316.0
- 007
- ta
- 008
- 131015s2012 xr d f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.932293 $2 doi
- 035 __
- $a (PubMed)22881227
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Riljak, Vladimír $u Institute of Physiology, First Faculty of Medicine, Charles University in Prague, Prague $7 xx0081611
- 245 10
- $a Nicotine and kainic acid effects on cortical epileptic afterdischarges in immature rats / $c V. Riljak, D. Marešová, K. Jandová, J. Pokorný
- 520 9_
- $a Aim of the study was to test the effect of nicotine (NIC) and kainic acid (KA) co-treatment in immature rats. Male Wistar albino rats (two different age groups) were chosen for the study. Experiments started on postnatal day (PD) 8 or 21 and animals were treated twice a day for three days with nicotine, fourth day KA was administered. Animals at PD12 (PD25 respectively) were examined electrophysiologically for cortical epileptic afterdischarges (ADs). First cortical ADs in PD12 animals were longer, when compared to PD25 rats (group treated with both substances). Nor NIC or KA treatment affected the length of discharges in PD12 rats. Older experimental group exhibited the shortening of the first ADs (group treated with NIC and KA, compared with groups exposed to single treatment). Few changes were found in KA treated group - 2(nd) and 4(th) ADs were shorter when compared with first ADs. These results demonstrate that NIC treatment played minor role in seizure susceptibility of PD12 rats, sensitivity to NIC differs during ontogenesis and subconvulsive dose of KA influenced the length of discharges only in PD25 animals.
- 650 _2
- $a akční potenciály $x účinky léků $7 D000200
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a novorozená zvířata $7 D000831
- 650 _2
- $a mozková kůra $x účinky léků $x patofyziologie $7 D002540
- 650 _2
- $a lékové interakce $7 D004347
- 650 _2
- $a epilepsie $x chemicky indukované $x patofyziologie $x prevence a kontrola $7 D004827
- 650 12
- $a kyselina kainová $7 D007608
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a nikotin $x aplikace a dávkování $7 D009538
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a výsledek terapie $7 D016896
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a randomizované kontrolované studie $7 D016449
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Marešová, Dana, $u Institute of Physiology, First Faculty of Medicine, Charles University in Prague, Prague $d 1946- $7 jn20000710437
- 700 1_
- $a Jandová, Kateřina, $u Institute of Physiology, First Faculty of Medicine, Charles University in Prague, Prague $d 1970- $7 xx0056834
- 700 1_
- $a Pokorný, Jaroslav, $u Institute of Physiology, First Faculty of Medicine, Charles University in Prague, Prague $d 1945- $7 jn20000710480
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 61, č. 5 (2012), s. 537-542
- 856 41
- $u http://www.biomed.cas.cz/physiolres/archive.htm $y domovská stránka časopisu - plný text volně přístupný = fulltext
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 3 $z 0
- 990 __
- $a 20131015 $b ABA008
- 991 __
- $a 20131024135601 $b ABA008
- 999 __
- $a ok $b bmc $g 998648 $s 831796
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2012 $b 61 $c 5 $d 537-542 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- LZP __
- $b NLK111 $a Pubmed-20131015