Abstract

Kindling is a permanent form of brain change that results from repeated elicitation of epileptiform neural activity, c- fos has been proposed as the gene responsible for turning on molecular events that might underlie the long-term changes that occur during kindling. This study investigated the enhancement of c- fos levels following kindled seizures and the role of c- fos in the plastic changes underlying kindling. Male hooded rats were electrically kindled in the amygdala and the resulting c- fos and c-Ha- ras gene expression was quantified using Northern blot hybridization analysis. The results indicated that c- fos was constitutively expressed in forebrain and cerebellum, and that basal levels of c- fos were equivalent in naive and in fully kindled rats that have been seizure-free for 3 weeks. Following an amygdala-piriform kindled seizure there was a massive and transient increase in c- fos levels throughout forebrain and cerebellum. Although enhanced c- fos levels were correlated with afterdischarge (AD) duration in the kindled site, enhanced c- fos levels were also observed in the amygdala-piriform contralateral to the kindled site, and the enhancement did not depend on the occurrence of AD in the contralateral amygdala-piriform. Furthermore, electrical stimulations not resulting in AD as well as other forms of control stimulation also increased c- fos levels. We conclude that c- fos was expressed simply as a consequence of neural activity and not exclusively due to the specific neural activity or underlying plastic change required for kindling. This does not preclude a role for c- fos in the long-term response to external stimuli, but it does suggest that c- fos is not the crucial ‘master switch’ in turning on a molecular program that might underlie kindling.

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