Cited by 109Neuropeptides and Animal PhysiologyStress Responses and CortisolNeurotransmitter Receptor Influence on Behavior

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Behavioral and Anatomical Interactions between Dopamine and Corticotropin-Releasing Factor in the Rat

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Meloni, Edward G., Gerety, Lyle P., Knoll, Allison T., Cohen, Bruce M., Carlezon, William A.·2006·The Journal of Neuroscience

DOI 10.1523/jneurosci.4957-05.2006PMC PMC6674129

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Abstract

The neuropeptide corticotropin-releasing factor (CRF) is believed to play a role in a number of psychiatric conditions, including anxiety disorders and depression. In the present study, male Sprague Dawley rats were used to examine the behavioral effects of altering dopamine transmission on CRF-enhanced startle, a behavioral assay believed to reflect stress- or anxiety-like states. Systemic administration of the selective dopamine D1 receptor antagonist SCH 23390 [R(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride] (0, 0.01, 0.05, 0.1, 0.5 mg/kg) dose dependently blocked the effect of CRF (1 microg, i.c.v.) on startle at doses that had no effect on baseline startle response. Immunohistochemical studies showed that most CRF-containing cells in the dorsolateral division of the bed nucleus of the stria terminalis (BSTld), part of the critical brain area mediating CRF-enhanced startle, are surrounded by a dense plexus of tyrosine hydroxylase (TH)-positive fibers. Intra-BSTld injections of the retrograde tracer Fluorogold (FG) into the TH field identified neurons in the major dopaminergic areas (A8-A10), but not the major noradrenergic areas [A5, A6 (locus ceruleus), A7], as a significant source of TH-positive innervation. The majority of FG-filled cells double-labeled for TH were found in the dorsocaudal A10 cell group (A10dc) located in the periaqueductal gray area. Together, these data suggest that neuronal regulation of the BSTld by specific dopaminergic pathways and receptors may be an important mechanism for controlling CRF-dependent moods and affective states. These data also suggest that compounds with D1 receptor antagonist properties might have anxiolytic-like effects that could be useful for treating conditions associated with hyperactive CRF systems.

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The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
Prevalence, Severity, and Comorbidity of 12-Month DSM-IV Disorders in the National Comorbidity Survey Replication
Kessler, R. C., Chiu, W. T., Demler, O., & Walters, E. E. (2005) · Archives of General Psychiatry · doi:10.1001/archpsyc.62.6.617 · Cited by 12,052
Handbook of Chemical Neuroanatomy
Stern, C. D. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90021-5 · Cited by 4,160
The rat nervous system
Paxinos, G. (1985) · Cited by 3,715
Allostasis and Allostatic Load Implications for Neuropsychopharmacology
McEwen, B. (2000) · Neuropsychopharmacology · doi:10.1016/s0893-133x(99)00129-3 · Cited by 1,833
The role of corticotropin-releasing factor in depression and anxiety disorders
Arborelius, L., Owens, M., Plotsky, P., & Nemeroff, C. (1999) · Journal of Endocrinology · doi:10.1677/joe.0.1600001 · Cited by 1,378
Physiological and behavioral responses to corticotropin-releasing factor administration: is CRF a mediator of anxiety or stress responses?
Dunn, A. J., & Berridge, C. W. (1990) · Brain Research Reviews · doi:10.1016/0165-0173(90)90012-d · Cited by 1,352
Organization of the stress system and its dysregulation in melancholic and atypical depression: high vs low CRH/NE states
Gold, P. W., & Chrousos, G. P. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001032 · Cited by 1,274
Localization of novel corticotropin-releasing factor receptor (CRF2) mRNA expression to specific subcortical nuclei in rat brain: comparison with CRF1 receptor mRNA expression
Chalmers, D., Lovenberg, T. W., & Souza, E. D. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-10-06340.1995 · Cited by 925
SCH 23390, a potential benzazepine antipsychotic with unique interactions on dopaminergic systems.
Iorio, L. C., Barnett, A., Leitz, F. H., Houser, V. P., & Korduba, C. A. (1983) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)21599-3 · Cited by 896

Show all 75 references

Research works printed but not linked: 2

(1983), J Pharmacol Exp Ther, 226, 462
(1984), Extrahypothalamic distribution. Peptides, 5, 53

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STUDY OF THE ROLE OF THE BED NUCLEUS OF THE STRIA TERMINALIS D1- AND D2-LIKE DOPAMINE RECEPTORS IN COCAINE SELF-ADMINISTERING RATS
Chiang, C.-J. C. (2015)

Authors: Meloni, E. G., Gerety, L. P., Knoll, A. T., Cohen, B. M., & Carlezon, W. A.
Affiliations: Harvard University (US)
ORCID: Meloni, Edward G.
Cohen, Bruce M.
Carlezon, William A.
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 2006-04-05
Volume: 26
Issue: 14
Pages: 3855-3863
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.4957-05.2006
PMC: PMC6674129
OpenAlex: W2063743575
Cited by: 109
References: 75
Citations by year: 2026: 1 · 2025: 6 · 2024: 2 · 2023: 5 · 2022: 5 · 2021: 7 · 2020: 3 · 2019: 3 · 2018: 5 · 2017: 9 · 2016: 3 · 2015: 5 · 2014: 6 · 2013: 10 · 2012: 7
FWCI: 2.15
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-sa
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 183 d)
Locations: Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: Stanley Medical Research Institute
National Institutes of Health (5r01mh063266-25)
National Institute of Mental Health (MH63266)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Keywords: corticotropin-releasing factor, dopamine, dopamine D1 receptor, SCH 23390, anxiety, stress, bed nucleus of the stria terminalis, tyrosine hydroxylase, dopaminergic innervation, periaqueductal gray, retrograde tracing, Fluoro-Gold, anxiolytic effects, noradrenergic neurons
MeSH terms: Animals, Behavior, Animal, Brain, Corticotropin-Releasing Hormone, Dopamine, Male, Reflex, Startle, Signal Transduction, Rats, Sprague-Dawley, Neurotransmitter Agents, Rats

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Behavioral and Anatomical Interactions between Dopamine and Corticotropin-Releasing Factor in the Rat

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