Literature DB >> 9622611

Infusion of the dopamine D1 receptor antagonist SCH 23390 into the amygdala blocks fear expression in a potentiated startle paradigm.

E W Lamont1, L Kokkinidis.   

Abstract

Dopamine (DA) D1 receptors are distributed in the nucleus accumbens and the amygdala, two regions of the mesocorticolimbic DA system known to be activated by aversive environmental stimuli. The objective of the present study was to determine the contribution of D1 receptors in these brain regions to the expression of a fear-motivated behavior, notably, potentiated startle in rats. Injection of the DA D1 receptor antagonist SCH 23390 into the amygdala blocked the ability of a conditioned light stimulus previously paired with footshock to enhance acoustic startle amplitudes. Bilateral intracerebral administration of SCH 23390 into the nucleus accumbens had no effect on fear-potentiated startle. The observed opposing effects of amygdaloid DA D1 receptor antagonism on fear expression, along with earlier research demonstrating the involvement of ventral tegmental area (VTA) DA neurons on fear-potentiated startle, suggest a role for mesoamygdaloid activity in conditioned excitatory fear reactions. Copyright 1998 Elsevier Science B.V. All rights reserved.

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Year:  1998        PMID: 9622611     DOI: 10.1016/s0006-8993(98)00281-9

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  30 in total

1.  Cellular mechanisms of infralimbic and prelimbic prefrontal cortical inhibition and dopaminergic modulation of basolateral amygdala neurons in vivo.

Authors:  J Amiel Rosenkranz; Anthony A Grace
Journal:  J Neurosci       Date:  2002-01-01       Impact factor: 6.167

2.  Dopamine attenuates prefrontal cortical suppression of sensory inputs to the basolateral amygdala of rats.

Authors:  J A Rosenkranz; A A Grace
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

3.  Modulation of basolateral amygdala neuronal firing and afferent drive by dopamine receptor activation in vivo.

Authors:  J A Rosenkranz; A A Grace
Journal:  J Neurosci       Date:  1999-12-15       Impact factor: 6.167

4.  Instrumental learning, but not performance, requires dopamine D1-receptor activation in the amygdala.

Authors:  M E Andrzejewski; R C Spencer; A E Kelley
Journal:  Neuroscience       Date:  2005       Impact factor: 3.590

5.  Low-frequency stimulation induces a pathway-specific late phase of LTP in the amygdala that is mediated by PKA and dependent on protein synthesis.

Authors:  Yan-You Huang; Eric R Kandel
Journal:  Learn Mem       Date:  2007-07-12       Impact factor: 2.460

Review 6.  The dopaminergic projection system, basal forebrain macrosystems, and conditioned stimuli.

Authors:  Daniel S Zahm; Michael Trimble
Journal:  CNS Spectr       Date:  2008-01       Impact factor: 3.790

7.  Distribution of D1 and D5 dopamine receptors in the primate and rat basolateral amygdala.

Authors:  E Chris Muly; Murat Senyuz; Zafar U Khan; Ji-Dong Guo; Rimi Hazra; Donald G Rainnie
Journal:  Brain Struct Funct       Date:  2009-08-08       Impact factor: 3.270

8.  Wiring and volume transmission in rat amygdala. Implications for fear and anxiety.

Authors:  Miguel Pérez de la Mora; Kirsten X Jacobsen; Minerva Crespo-Ramírez; Candy Flores-Gracia; Kjell Fuxe
Journal:  Neurochem Res       Date:  2008-05-13       Impact factor: 3.996

Review 9.  Establishing causality for dopamine in neural function and behavior with optogenetics.

Authors:  Elizabeth E Steinberg; Patricia H Janak
Journal:  Brain Res       Date:  2012-09-29       Impact factor: 3.252

Review 10.  The heterogeneity of ventral tegmental area neurons: Projection functions in a mood-related context.

Authors:  J J Walsh; M H Han
Journal:  Neuroscience       Date:  2014-06-12       Impact factor: 3.590

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