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Impact of Corticotropin‐Releasing Hormone on Extracellular Norepinephrine in Prefrontal Cortex After Chronic Cold Stress
Author(s) -
Finlay Janet M.,
Jedema Hank P.,
Rabinovic Ariel D.,
Mana Michael J.,
Zigmond Michael J.,
Sved Alan F.
Publication year - 1997
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.1997.69010144.x
Subject(s) - prefrontal cortex , extracellular , microdialysis , norepinephrine , endocrinology , medicine , chemistry , sensitization , dopamine , neuroscience , biology , biochemistry , cognition
We have previously demonstrated that exposing rats to cold (5°C) for 3–4 weeks potentiates the increase in extracellular norepinephrine (NE) in the medial prefrontal cortex produced by acute tail shock. In the present study, we used microdialysis to determine the duration of cold exposure required to produce this sensitization and explored the mechanism of the phenomenon. Tail shock elicited a twofold greater increase in extracellular NE in the medial prefrontal cortex of rats exposed to cold for 2 weeks than in naive control rats or in rats exposed to cold for 1 week and tested either immediately or after a 2‐week delay. Local infusion of 10 µ M d ‐amphetamine or 30 m M K + increased extracellular NE in the medial prefrontal cortex (∼350 and 190%, respectively) comparably in control rats and rats exposed to cold for 3 weeks. In contrast, intraventricular administration of 3.0 µg of corticotropin‐releasing hormone increased extracellular NE in the medial prefrontal cortex by 65% in rats exposed to cold for 2 weeks, but only 35% in control rats. These results indicate that an enhanced responsiveness of noradrenergic neurons to acute tail shock (1) requires ∼2 weeks of cold exposure to develop and (2) may be mediated by a change at the level of the noradrenergic cell bodies rather than the nerve terminals.