Abstract
One component of the nocturnal changes in cellular immediate-early gene expression in the rat pineal gland is a decrease in c- jun expression, mediated through ß-adrenoceptors. An in vitro study of the intracellular mechanisms which control c- jun expression has now shown that a norepinephrine-induced increase in c- jun mRNA levels in organ-cultured pineals is differentially modulated by protein kinase inhibitors; N-(2-guanidinoethyl)-5-isoquinolinesulfonamide (HA-1004) potentiated the response; however, in the presence of 1-(5-isoquinolinylsulfonyl)-2-methylpiperazine (H-7), a significant decrease in c- jun mRNA was found. Treatment with HA-1004 alone elevated the level of c- jun mRNA, H-7 alone was without effect. Forskolin together with 3-isobutyl-1-methylxanthine suppressed c- jun, whereas phorbol 12,13-dibutyrate raised c- jun mRNA levels. The results demonstrate opposing pathways for c- jun regulation in the pineal gland, and indicate that the nocturnal attenuation of c- jun expression involves selective activation of a negative pathway which may be linked to cAMP.
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More From: European Journal of Pharmacology: Molecular Pharmacology
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