DIFFERENTIAL-EFFECTS OF HYPOTHYROIDISM ON NA-K-ATPASE MESSENGER-RNA ALPHA-ISOFORM IN THE DEVELOPING RAT-BRAIN

Citation
S. Chaudhury et al., DIFFERENTIAL-EFFECTS OF HYPOTHYROIDISM ON NA-K-ATPASE MESSENGER-RNA ALPHA-ISOFORM IN THE DEVELOPING RAT-BRAIN, Journal of molecular neuroscience, 7(3), 1996, pp. 229-234
Citations number
25
Categorie Soggetti
Biology,Neurosciences
ISSN journal
08958696
Volume
7
Issue
3
Year of publication
1996
Pages
229 - 234
Database
ISI
SICI code
0895-8696(1996)7:3<229:DOHONM>2.0.ZU;2-9
Abstract
In the developing rat cerebrum, the level of different isoforms of Na- K-ATPase mRNA increases significantly during the first three postnatal weeks, which represent the critical period of synaptogenesis and myel ination-the two thyroid hormone-sensitive maturational events. To dete rmine the possible functional relationship of these isoforms with matu rational events in the developing brain and their mode of regulation b y T-3, we have examined the effect of hypothyroidism on the expression of the different alpha-isoforms (alpha 1, alpha 2, and alpha 3) of Na -K-ATPase mRNA covering the first 3 wk of postnatal development. Quant itation of these mRNAs from cerebra of 1-, 5-, 10-, 15-, and 20-d-old normal and hypothyroid rats by Northern blot analysis indicate that al pha 3 mRNA is not only predominantly expressed throughout this entire period of study but also represents the species which is most severely affected in the hypothyroid brain. The relative sensitivity for the e xpression of these mRNAs to T-3 were alpha 3> alpha 1> alpha 2. These results, together with the report of predominant expression of the alp ha 3 isoform in neuronal cells, suggest specific functional involvemen t of this isoform with the decisive maturational events in the rat bra in. Kinetic studies on in vivo induction of Na-K-ATPase alpha-mRNAs by T-3 in the 15-d-old hypothyroid rat shows clear stimulation of all th e isoforms within 1 h of the administration of the optimal dose (200 m u g T-3/100 g body wt) suggesting a direct, possibly transcriptional e ffect of the hormone on the expression of these genes.