Hyperthermia aggravates status epilepticus-induced epileptogenesis and neuronal loss in immature rats
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
NS074926
NINDS NIH HHS - United States
NS059704
NINDS NIH HHS - United States
R01 NS013515
NINDS NIH HHS - United States
NS13515
NINDS NIH HHS - United States
I01 BX000273
BLRD VA - United States
U01 NS074926
NINDS NIH HHS - United States
R21 NS059704
NINDS NIH HHS - United States
PubMed
26259902
DOI
10.1016/j.neuroscience.2015.08.006
PII: S0306-4522(15)00729-0
Knihovny.cz E-zdroje
- Klíčová slova
- EEG monitoring, immature brain, lithium/pilocarpine model, neuronal injury, temperature,
- MeSH
- adjuvancia imunologická toxicita MeSH
- agonisté muskarinových receptorů toxicita MeSH
- antikonvulziva terapeutické užití MeSH
- apoptóza účinky léků fyziologie MeSH
- buněčná smrt účinky léků MeSH
- časové faktory MeSH
- chlorid lithný toxicita MeSH
- degenerace nervu etiologie MeSH
- diazepam terapeutické užití MeSH
- indukovaná hypertermie škodlivé účinky MeSH
- krysa rodu Rattus MeSH
- modely nemocí na zvířatech MeSH
- mozek účinky léků patologie patofyziologie ultrastruktura MeSH
- neurony patologie ultrastruktura MeSH
- neuropil patologie ultrastruktura MeSH
- novorozená zvířata MeSH
- pilokarpin toxicita MeSH
- potkani Wistar MeSH
- status epilepticus etiologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- adjuvancia imunologická MeSH
- agonisté muskarinových receptorů MeSH
- antikonvulziva MeSH
- chlorid lithný MeSH
- diazepam MeSH
- pilokarpin MeSH
This study tightly controlled seizure duration and severity during status epilepticus (SE) in postnatal day 10 (P10) rats, in order to isolate hyperthermia as the main variable and to study its consequences. Body temperature was maintained at 39 ± 1 °C in hyperthermic SE rats (HT+SE) or at 35 ± 1 °C in normothermic SE animals (NT+SE) during 30 min of SE, which was induced by lithium-pilocarpine (3 mEq/kg, 60 mg/kg) and terminated by diazepam and cooling to NT. All video/EEG measures of SE severity were similar between HT+SE and NT+SE pups. At 24h, neuronal injury was present in the amygdala in the HT+SE group only, and was far more severe in the hippocampus in HT+SE than NT+SE pups. Separate groups of animals were monitored four months later for spontaneous recurrent seizures (SRS). Only HT+SE animals developed convulsive SRS. Both HT+SE and NT+SE animals developed electrographic SRS (83% vs. 55%), but SRS frequency and severity were higher in hyperthermic animals (12.5 ± 3.5 vs. 4.2 ± 2.0 SRS/day). The density of hilar neurons was lower, thickness of the amygdala and perirhinal cortex was reduced, and lateral ventricles were enlarged in HT+SE over NT+SE littermates and HT/NT controls. In this model, hyperthermia greatly increased the epileptogenicity of SE and its neuropathological sequelae.
Citace poskytuje Crossref.org
Epilepsy Research in the Institute of Physiology of the Czech Academy of Sciences in Prague
The outcome of early life status epilepticus-lessons from laboratory animals