Heightened transcription for enzymes involved in norepinephrine biosynthesis in the rat locus coeruleus by immobilization stress

Citation
Li. Serova et al., Heightened transcription for enzymes involved in norepinephrine biosynthesis in the rat locus coeruleus by immobilization stress, BIOL PSYCHI, 45(7), 1999, pp. 853-862
Citations number
62
Categorie Soggetti
Neurosciences & Behavoir
Journal title
BIOLOGICAL PSYCHIATRY
ISSN journal
00063223 → ACNP
Volume
45
Issue
7
Year of publication
1999
Pages
853 - 862
Database
ISI
SICI code
0006-3223(19990401)45:7<853:HTFEII>2.0.ZU;2-Z
Abstract
Background: The locus coeruleus (LC), a target for CRH neurons, is critical ly involved in responses to stress. Various physiological stresses increase norepinephrine turnover, tyrosine hydroxylase (TH) enzymatic activity, pro tein and mRNA levels in LC cell bodies and terminals; however, the effect o f stress on other enzymes involved in norepinephrine biosynthesis in the LC in unknown. Methods: Rats were exposed to single (2 hour) or repeated (2 hour daily) im mobilization stress (IMO). Recombinant rat dopamine b-hydroxylase (DBH) cDN A was expressed in E. coli and used to generate antisera for immunohistoche mistry and immunoblots in LC. Northern blots were used to assess changes in mRNA levels for TH, DBH, and GTP cyclohydrolase I (GTPCH) in the LC in res ponse to the stress. Conditions were found to isolate nuclei from LC and to use them for run-on assays of transcription. Results: Repeated stress elevated the DBH immunoreactive protein levels in LC. Parallel increases in TH, DBH and GTPCH mRNA levels of about 300% to 40 0% over control levels were observed with single IMO, and remained at simil ar levels after repeated IMO. This effect was transcriptionally mediated, a nd even 30 min of a single IMO significantly increased the relative rate of transcription. Conclusions: This study is the first to reveal transcriptional activation o f the genes encoding catecholamine biosynthetic enzymes in the LC by stress . In addition to TH, changes in DBH and GTPCH gene expression may also cont ribute to the development of stress-triggered affective disorders. (C) 1999 Society of Biological Psychiatry.