PROTEIN-SYNTHESIS BLOCKADE DIFFERENTIALLY AFFECTS THE STRESS-INDUCED TRANSCRIPTIONAL ACTIVATION OF NEUROPEPTIDE GENES IN PARVOCELLULAR NEUROSECRETORY NEURONS
Coaicotropin-releasing factor (CRF) and arginine vasopressin (AVP) are
synergistically interacting ACTH secretagogues that are co-expressed
by parvocellular neurosecretory neurons of the hypothalamic paraventri
cular nucleus (PVH). To shed light on the mechanisms that mediate the
stress-induced transcriptional activation of these neuropeptide genes,
quantitative hybridization histochemical methods were used to assess
the effects of systemic treatment with the protein synthesis inhibitor
, cycloheximide, on the ether stress-induced upregulation of primary C
RF and AVP transcripts, in vivo. Pretreatment with cycloheximide preve
nted the induction of Fos, but not CREB phosphorylation, normally seen
in response to acute ether exposure, and significantly attenuated the
stress-induced rise in AVP, but not CRF, heteronuclear RNA expression
in the parvocellular division of the PVH. These results support the v
iew that distinct molecular mechanisms govern the expression of the tw
o principal corticotropin-releasing factors, in vivo. (C) 1998 Elsevie
r Science B.V.