Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/26182
Title: Increased sensitivity to seizures in mice lacking cellular prion protein
Authors: Walz, Roger
Amaral, Olavo B.
Rockenbach, Isabel C.
Roesler, Rafael
Izquierdo, Ivan
Cavalheiro, Esper Abrão [UNIFESP]
Martins, Vilma R.
Brentani, Ricardo R.
Univ Fed Rio Grande Sul
Universidade Federal de São Paulo (UNIFESP)
Ludwig Inst Canc Res
Keywords: prion
PrPc
seizure
epilepsy
kindling
Issue Date: 1-Dec-1999
Publisher: Lippincott Williams & Wilkins
Citation: Epilepsia. Philadelphia: Lippincott Williams & Wilkins, v. 40, n. 12, p. 1679-1682, 1999.
Abstract: Purpose: the physiologic role of the cellular prion protein (PrPc) is unknown. Mice devoid of PrPc develop normally and show only minor deficits. However, electrophysiologic and histologic alterations found in these mice suggest a possible:role fur PrPc in seizure threshold and/or epilepsy.Methods: We tested the sensitivity of PrPc knockout mice to seizures induced by single convulsant or repeated subconvulsant (kindling) doses of pentylenetetrazol (PTZ), and to status epilepticus (SE) induced by kainic acid or pilocarpine.Results. in PTZ kindling, seizure severity progressed faster in the PrPc knockout group, in which 92.8% reached stage 5 or death after 4 days of stimulation, as opposed to 38.4% in wildtype animals: After 10 injections, mortality was 85.7% among knockouts and 15.3% among controls. After a single PTZ injection (60 mg/kg), overall mortality due to seizures was 91% in knockout mice, but only 33% among wild-type animals. Pilocarpine-induced SE (320 mg/kg) caused an 86.7% mortality in knockouts, as opposed to 40% in wild-type animals. Finally, after kainic acid injections (10 mg/kg), 70% of the knockouts developed at least one severe seizure, and 50% showed repetitive seizures, whereas no wild-type animal exhibited observable seizures.Conclusions: Animals lacking cellular prion protein expression are more susceptible to seizures induced by various convulsant agents. This is perhaps the most striking alteration yet found in PrPc-null mice, who at first analysis appeared to be completely normal. A possible role for PrPc in chronic and idiopathic (familial), secondary, or cryptogenic epilepsies in humans remains to be investigated.
URI: http://repositorio.unifesp.br/handle/11600/26182
ISSN: 0013-9580
Other Identifiers: http://dx.doi.org/10.1111/j.1528-1157.1999.tb01583.x
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