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Quantification of extracellular levels of corticosterone in the basolateral amygdaloid complex of freely-moving rats: A dialysis study of circadian variation and stress-induced modulation

Abstract Corticosterone influences emotion and cognition via actions in a diversity of corticolimbic structures, including the amygdala. Since extracellular levels of corticosterone in brain have rarely been studied, we characterized a specific and sensitive enzymatic immunoassay for microdialysis q...

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Published in:Brain research 2012-05, Vol.1452, p.47-60
Main Authors: Bouchez, Gaëlle, Millan, Mark J, Rivet, Jean-Michel, Billiras, Rodolphe, Boulanger, Raphaël, Gobert, Alain
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container_title Brain research
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description Abstract Corticosterone influences emotion and cognition via actions in a diversity of corticolimbic structures, including the amygdala. Since extracellular levels of corticosterone in brain have rarely been studied, we characterized a specific and sensitive enzymatic immunoassay for microdialysis quantification of corticosterone in the basolateral amygdaloid complex of freely-moving rats. Corticosterone levels showed marked diurnal variation with an evening (dark phase) peak and stable, low levels during the day (light phase). The “anxiogenic agents”, FG7142 (20 mg/kg) and yohimbine (10 mg/kg), and an environmental stressor, 15-min forced-swim, induced marked and sustained (1–3 h) increases in dialysis levels of corticosterone in basolateral amygdaloid complex. They likewise increased dialysis levels of dopamine and noradrenaline, but not serotonin and GABA. As compared to basal corticosterone levels of ~ 200–300 pg/ml, the elevation provoked by forced-swim was ca. 20-fold and this increase was abolished by adrenalectomy. Interestingly, stress-induced rises of corticosterone levels in basolateral amygdaloid complex were abrogated by combined but not separate administration of the corticotrophin releasing factor1 (CRF1 ) receptor antagonist, CP154,526, and the vasopressin1b (V1b ) receptor antagonist, SSR149,415. Underpinning their specificity, they did not block forced-swim-induced elevations in dopamine and noradrenaline. In conclusion, extracellular levels of corticosterone in the basolateral amygdaloid complex display marked diurnal variation. Further, they are markedly elevated by acute stressors, the effects of which are mediated (in contrast to concomitant elevations in levels of monoamines) by co-joint recruitment of CRF1 and V1b receptors.
doi_str_mv 10.1016/j.brainres.2012.01.010
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Interestingly, stress-induced rises of corticosterone levels in basolateral amygdaloid complex were abrogated by combined but not separate administration of the corticotrophin releasing factor1 (CRF1 ) receptor antagonist, CP154,526, and the vasopressin1b (V1b ) receptor antagonist, SSR149,415. Underpinning their specificity, they did not block forced-swim-induced elevations in dopamine and noradrenaline. In conclusion, extracellular levels of corticosterone in the basolateral amygdaloid complex display marked diurnal variation. 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Interestingly, stress-induced rises of corticosterone levels in basolateral amygdaloid complex were abrogated by combined but not separate administration of the corticotrophin releasing factor1 (CRF1 ) receptor antagonist, CP154,526, and the vasopressin1b (V1b ) receptor antagonist, SSR149,415. Underpinning their specificity, they did not block forced-swim-induced elevations in dopamine and noradrenaline. In conclusion, extracellular levels of corticosterone in the basolateral amygdaloid complex display marked diurnal variation. 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Psychology</topic><topic>gamma-Aminobutyric Acid - metabolism</topic><topic>immunoassays</topic><topic>Microdialysis</topic><topic>monoamines</topic><topic>Neurology</topic><topic>norepinephrine</topic><topic>Norepinephrine - metabolism</topic><topic>Rats</topic><topic>receptors</topic><topic>recruitment</topic><topic>serotonin</topic><topic>Serotonin - metabolism</topic><topic>Stress</topic><topic>Stress, Psychological - metabolism</topic><topic>Vasopressin</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>yohimbine</topic><topic>Yohimbine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bouchez, Gaëlle</creatorcontrib><creatorcontrib>Millan, Mark J</creatorcontrib><creatorcontrib>Rivet, Jean-Michel</creatorcontrib><creatorcontrib>Billiras, Rodolphe</creatorcontrib><creatorcontrib>Boulanger, Raphaël</creatorcontrib><creatorcontrib>Gobert, Alain</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bouchez, Gaëlle</au><au>Millan, Mark J</au><au>Rivet, Jean-Michel</au><au>Billiras, Rodolphe</au><au>Boulanger, Raphaël</au><au>Gobert, Alain</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantification of extracellular levels of corticosterone in the basolateral amygdaloid complex of freely-moving rats: A dialysis study of circadian variation and stress-induced modulation</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2012-05-03</date><risdate>2012</risdate><volume>1452</volume><spage>47</spage><epage>60</epage><pages>47-60</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Abstract Corticosterone influences emotion and cognition via actions in a diversity of corticolimbic structures, including the amygdala. 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Interestingly, stress-induced rises of corticosterone levels in basolateral amygdaloid complex were abrogated by combined but not separate administration of the corticotrophin releasing factor1 (CRF1 ) receptor antagonist, CP154,526, and the vasopressin1b (V1b ) receptor antagonist, SSR149,415. Underpinning their specificity, they did not block forced-swim-induced elevations in dopamine and noradrenaline. In conclusion, extracellular levels of corticosterone in the basolateral amygdaloid complex display marked diurnal variation. Further, they are markedly elevated by acute stressors, the effects of which are mediated (in contrast to concomitant elevations in levels of monoamines) by co-joint recruitment of CRF1 and V1b receptors.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>22464880</pmid><doi>10.1016/j.brainres.2012.01.010</doi><tpages>14</tpages></addata></record>
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source ScienceDirect Journals
subjects Amygdala
Amygdala - drug effects
Amygdala - metabolism
Animals
antagonists
Biological and medical sciences
Carbolines - pharmacology
Chronobiology
Circadian Rhythm - physiology
cognition
Corticosterone
Corticosterone - metabolism
Corticosterone - pharmacology
corticotropin
CRF
diurnal variation
dopamine
Dopamine - metabolism
Fundamental and applied biological sciences. Psychology
gamma-Aminobutyric Acid - metabolism
immunoassays
Microdialysis
monoamines
Neurology
norepinephrine
Norepinephrine - metabolism
Rats
receptors
recruitment
serotonin
Serotonin - metabolism
Stress
Stress, Psychological - metabolism
Vasopressin
Vertebrates: anatomy and physiology, studies on body, several organs or systems
yohimbine
Yohimbine - pharmacology
title Quantification of extracellular levels of corticosterone in the basolateral amygdaloid complex of freely-moving rats: A dialysis study of circadian variation and stress-induced modulation
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