Abstract

Astrocytes from various regions of CNS have been shown to express voltage-activated Na + currents. To date, three distinct subtypes (I, II and III) of Na + channels have been cloned from rat brain. We have applied a combined technique of reverse transcription and polymerase chain reaction (RT-PCR) to examine the expression of rat brain Na + channels in rat astrocytes in vivo and in vitro. Five PCR primer sets were used to amplify coding or 3′ non-coding regions of subtype I, II, and III Na + channels. We were able to amplify all three of these rat brain Na + channel subtypes from rat optic nerve, which does not have neuronal cell bodies but does contain astrocytes known to express voltage-sensitive Na + channels. In studies on cultured spinal cord astrocytes, we were also able to amplify all three subtypes of rat brain Na + channel mRNAs. In control experiments, RT-PCR was performed on RNAs prepared from several rat tissues, including brain, skeletal muscle, and liver. Rat brain was shown to express the three Na + channel subtypes as expected. In rat skeletal muscle, subtype I and III Na + channel mRNAs, but not subtype II, were amplified. In rat liver, Na + channel messages were not detectable. The present study provides the first direct evidence that astrocytes in vivo and in vitro express rat brain voltage-sensitive Na + channel mRNAs, which have been considered as mainly neuronal-type Na + channel messages.

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