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Neurochemical and behavioral effects of corticotropin-releasing factor in the ventral tegmental area of the rat
Abstract
Corticotropin-releasing factor (CRF) is thought to have a neurotransmitter function in the mammalian central nervous system. The release of CRF into the hypothalamic-hypophyseal portal system in response to stress is known, and it has been suggested that CRF may function elsewhere in the central nervous system to promote stress-induced physiological and behavioral changes. Acute stress has been shown to activate dopamine (DA) neurons in the ventral tegmental area (VTA) that project to the prefrontal cortex. To determine whether CRF may act in the VTA to activate the mesocortical or mesolimbic DA systems, it was injected into the VTA of rats, and changes in spontaneous motor behavior and DA metabolism were measured. Intra-VTA injection of CRF produced a dose-dependent increase in horizontal and vertical photocell counts with a minimal effective dose of 0.01 and 0.1 nmol, respectively. In contrast, the minimal effective dose for CRF-stimulated motor behavior after injection into the lateral ventricles was 0.3 nmol for horizontal activity. Furthermore, in the open field, the behavioral profile of CRF (0.3 nmol) given intra-VTA differed from that observed after intraventricular injection. The motor stimulant effect of intra-VTA CRF was not blocked by pretreatment with the DA receptor antagonist haloperidol. After intra-VTA injection, CRF produced a dose-dependent decrease in DA metabolism in the prefrontal cortex. The decrease in DA metabolism in the prefrontal cortex was present at 30 and 60 min but not at 120 min after injection, and in the nucleus accumbens DA metabolism was increased only at 60 min after injection.(ABSTRACT TRUNCATED AT 250 WORDS)
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“Postnatally, CRF and glucocorticoids can potentiate dopamine release (Bagosi et al., 2006; Kalivas et al., 1987; Piazza et al., 1996).”
From The effects of early life stress on reward processing (2018) · cites this paper as Kalivas et al., 1987
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“, 2004), stimulate locomotion and the mesocorticolimbic dopamine system (Kalivas et al., 1987), a system that is also implicated in drug reward (Wise and Bozarth, 1987) and drug-seeking behavior (Stewart, 1984).”
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“Previous studies have shown that CRF induces sensitization to the locomotor activating effects of d-amphetamine (Cador et al., 1993) and increases DA utilization in the prefrontal cortex and the nucleus accumbens (Dunn and Berridge, 1987; Lavicky and Dunn, 1993; but see Kalivas et al., 1987).”
BackgroundSevere stress switches CRF action in the nucleus accumbens from appetitive to aversive
Lemos, J. C., Wanat, M. J., Smith, J. S., Reyes, B. A. S., Hollon, N. G., Bockstaele, E. J. V., Chavkin, C., & Phillips, P. E. M. (2012) · Nature · doi:10.1038/nature11436 · Cited by 319
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“2000) or directly into the VTA (Kalivas et al. 1987) increases locomotor activity, and the effect of ventricular infusions of CRF on motor activity is absent in CRF-R1−/– mice (Contarino et al.”
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Region-specific roles of the corticotropin-releasing factor–urocortin system in stress
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Chapter 19 The determinants of stress-induced activation of the prefrontal cortical dopamine system
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The effects of early life stress on reward processing
Novick, A. M., Levandowski, M. L., Laumann, L. E., Philip, N. S., Price, L. H., & Tyrka, A. R. (2018) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2018.02.002 · Cited by 192
“Postnatally, CRF and glucocorticoids can potentiate dopamine release (Bagosi et al., 2006; Kalivas et al., 1987; Piazza et al., 1996).”
BackgroundSwiergiel, A. H., Takahashi, L. K., & Kalin, N. H. (1993) · Brain Research · doi:10.1016/0006-8993(93)91432-r · Cited by 199
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Allostasis and addiction: role of the dopamine and corticotropin-releasing factor systems
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The CRF Family of Neuropeptides and their Receptors - Mediators of the Central Stress Response
Dedic, N., Chen, A., & Deussing, J. M. (2017) · Current Molecular Pharmacology · doi:10.2174/1874467210666170302104053 · Cited by 187
“Accordingly, CRF was shown to increase dopamine neuron firing and dopamine release [106, 150-155], although opposite results were also observed depending on the study-design and the investigated release sites [150, 151].”
ResultLavický, J., & Dunn, A. J. (1993) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1993.tb03191.x · Cited by 176
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“…(NMDA) receptor-mediated synaptic transmission in dopamine neurons in the VTA (Ungless et al., 2003); intraVTA injection of CRF produced an increase in spontaneous motor activity in rats (Kalivas et al., 1987) and foot-shock stress caused a release of CRF in the VTA (Wang et al., 2005).”
BackgroundThe Role of CRF in Behavioral Aspects of Stress
Heinrichs, S. C., Menzaghi, F., Pich, E. M., Britton, K. T., & Koob, G. F. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb44673.x · Cited by 160
Regulation of behavioral responses by corticotropin-releasing factor
Lowry, C. A., & Moore, F. L. (2006) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2005.12.006 · Cited by 156
Feelings about food: the ventral tegmental area in food reward and emotional eating
Meye, F. J., & Adan, R. A. H. (2013) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2013.11.003 · Cited by 164
VTA CRF neurons mediate the aversive effects of nicotine withdrawal and promote intake escalation
Grieder, T. E., Herman, M. A., Contet, C., Tan, L. A., Vargas-Pérez, H., Cohen, A., Chwalek, M., Maal‐Bared, G., Freiling, J., Schlosburg, J. E., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3872 · Cited by 132
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“For example, CRF infusion into the ventral tegmentum significantly increased dopamine turnover in the nucleus accumbens (Kalivas et al., 1987), a brain region in which increased dopamine release disrupts PPI (Swerdlow et al.”
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Pecoraro, N. C., Dallman, M. F., Warne, J. P., Ginsberg, A. B., Laugero, K. D., la Fleur, S. E., Houshyar, H., Gómez-Oliver, F., Bhargava, A., & Akana, S. F. (2006) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2006.07.004 · Cited by 125
CRF acts in the midbrain to attenuate accumbens dopamine release to rewards but not their predictors
Wanat, M. J., Bonci, A., & Phillips, P. E. M. (2013) · Nature Neuroscience · doi:10.1038/nn.3335 · Cited by 113
A ventral tegmental CRF–glutamate–dopamine interaction in addiction
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“…signaling to dopamine neurons, implicated by the electrophysiological studies of Ungless et al. (2003) and first suggested by the histological studies of Swanson et al. (1983) and the intracranial injection studies of Kalivas et al. (1987), is confirmed by our microdialysis and anatomical studies.”
BackgroundResultTagliaferro, P. A., & Morales, M. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21576 · Cited by 107
“…1999; Vale et al., 1981) by interacting with different neuronal pathways, such as the hypothalamic-pituitary-adrenal (HPA) circuit (Bale and Vale, 2004; Dunn and Berridge, 1990; Vale et al., 1981) and the mesocorticolimbic dopamine (DA) system (Deutch and Roth, 1990; Kalivas et al., 1987).”
BackgroundPsychological and neural mechanisms of relapse
Stewart, J. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0084 · Cited by 113
“…responses to stress including fear and anxiety (Schulkin et al. 2005; Davis 2006); in addition, CRF has been shown to facilitate locomotor activity (Kalivas et al. 1987; Cador et al. 1993) and responses to positive incentive stimuli (Pecina et al. 2006), responses involved in appetitive behaviour.”
Blacktop, J. M., Seubert, C., Baker, D. L., Ferda, N., Lee, G., Graf, E. N., & Mantsch, J. R. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1393-11.2011 · Cited by 102
“Accordingly, delivery of CRF into the VTA stimulates local and terminal field dopamine release (Kalivas et al., 1987; Wang et al., 2005).”
Bryce, C. A., & Floresco, S. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.15 · Cited by 102
“However, intra-VTA CRF infusions reduce dopamine metabolism in the PFC and increases DA metabolism in the NAc 60 min following infusion (Kalivas et al, 1987).”
BackgroundNeuroregulation of nonexercise activity thermogenesis and obesity resistance
Kotz, C. M., Teske, J. A., & Billington, C. J. (2007) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00095.2007 · Cited by 103
“Corticotropin-releasing hormone, increases spontaneous physical activity after intracerebroventricular (74–76, 101) and site-specific (38, 61, 69, 82, 100, 106, 140) administration, although corticotropin-releasing hormone has no effect on spontaneous physical activity after administration into some brain areas, inclu…”
BackgroundMantsch, J. R., Baker, D. L., Francis, D. M., Katz, E. S., Hoks, M. A., & Serge, J. P. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0950-5 · Cited by 98
“CRFinduced increases in extracellular DA in the NAcc have also been found (Kalivas et al. 1987).”
InfluentialEffects of the CRH Receptor Antagonist CP-154,526 on Intravenous Cocaine Self-administration in Rats
Goeders, N. (2000) · Neuropsychopharmacology · doi:10.1016/s0893-133x(00)00148-2 · Cited by 94
“ICV CRH has little or no effect on dopamine in the nucleus accumbens (Kalivas et al. 1987; Dunn and Berridge 1990) and actually increases dopamine metabolism in the medial prefrontal cortex (Dunn and Berridge 1990).”
BackgroundBoyson, C. O., Miguel, T. T., Quadros, I. M., DeBold, J. F., & Miczek, K. A. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2266-8 · Cited by 92
“These activational effects within the VTA most likely involve downstream elevation of DA and activation of DA receptors in the mPFC and Acb (Capriles et al. 2003; McFarland et al. 2004; Kalivas et al. 1987).”
BackgroundNociceptin/orphanin FQ and drugs of abuse
Ciccocioppo, R., Angeletti, S., Panocka, I., & Massi, M. (2000) · Peptides · doi:10.1016/s0196-9781(00)00245-x · Cited by 92
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Cador, M., Cole, B. J., Koob, G. F., Stinus, L., & Moal, M. L. (1993) · Brain Research · doi:10.1016/0006-8993(93)90982-s · Cited by 87
The Role of Limbic and Hypothalamic Corticotropin‐Releasing Factor in Behavioral Responses to Stress
Menzaghi, F., Heinrichs, S. C., Pich, E. M., Weiss, F., & Koob, G. F. (1993) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1993.tb49929.x · Cited by 86
Hahn, J., Hopf, F. W., & Bonci, A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4773-08.2009 · Cited by 83
“Injection of CRF directly into the VTA increases locomotor activity (Kalivas et al., 1987) and drug taking (Wang et al., 2005), whereas injection of CRF antagonists inhibits stress-induced reinstatement of cocaine seeking (Wang et al., 2005, 2007).”
BackgroundA final common pathway for depression? Progress toward a general conceptual framework
Stone, E. A., Lin, Y., & Quartermain, D. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.08.007 · Cited by 85
“Also CRF stimulates motor behavior from the ventral tegmental area (Kalivas et al., 1987).”
BackgroundClements, S., Schreck, C. B., Larsen, D. A., & Dickhoff, W. W. (2002) · General and Comparative Endocrinology · doi:10.1006/gcen.2001.7707 · Cited by 82
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Corticotropin-releasing factor induces a place aversion independent of its neuroendocrine role
Cador, M., Ahmed, S. H., Koob, G. F., Le Moal, M., & Stinus, L. (1992) · Brain Research · doi:10.1016/0006-8993(92)91487-y · Cited by 74
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“…including fish (Clements et al., 2002; Clements and Schreck, 2004a; Bernier and Craig, 2005; Bernier, 2006), amphibians (Lowry et al., 1990; Lowry and Moore, 1991; Lowry et al., 1996; Crespi and Denver, 2004), birds (Zhang et al., 2001a; Zhang et al., 2001b) and rodents (Kalivas et al., 1987).”
BackgroundWang, H., & Morales, M. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21751 · Cited by 70
“PUBLISHED 2008 WILEY-LISS, INC. †This article is a US Government work and, as such, is in the public domain in the United States of America. injections of CRF into the VTA (Kalivas et al., 1987).”
BackgroundYamamoto, H., Maeda, T., Fujimura, M., & Fujimiya, M. (1998) · Neuroscience Letters · doi:10.1016/s0304-3940(98)00071-8 · Cited by 68
Borsody, M. K., & Weiss, J. M. (1996) · Brain Research · doi:10.1016/0006-8993(96)00199-0 · Cited by 65
Lowry, C. A., Burke, K. A., Renner, K. J., Moore, F. L., & Orchinik, M. (2001) · Hormones and Behavior · doi:10.1006/hbeh.2001.1646 · Cited by 61
Holahan, M. R., Kalin, N. H., & Kelley, A. E. (1997) · Psychopharmacology · doi:10.1007/s002130050228 · Cited by 60
Hwa, L. S., Holly, E. N., DeBold, J. F., & Miczek, K. A. (2015) · Psychopharmacology · doi:10.1007/s00213-015-4144-2 · Cited by 61
“These current results appear to contrast with past studies demonstrating CRF increasing dopamine neuron firing and release (Kalivas et al. 1987; Wanat et al. 2008) while CRF receptor antagonists in the VTA reduce glutamate and dopamine release in the VTA (Wang et al. 2005).”
Conti, L. H., Murry, J., Ruiz, M., & Printz, M. P. (2002) · Psychopharmacology · doi:10.1007/s00213-002-1025-2 · Cited by 59
Finlay, J. M., Jedema, H. P., Rabinovic, A. D., Mana, M. J., Zigmond, M. J., & Sved, A. F. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.69010144.x · Cited by 57
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“GR blockade may therefore attenuate CRF-induced excitation of dopamine neurons during stress (Kalivas et al., 1987; Ungless et al., 2003; Wanat et al., 2008; Holly et al., 2015).”
BackgroundGender Difference in Cocaine-Induced HPA Axis Activation
Kuhn, C. M. (1997) · Neuropsychopharmacology · doi:10.1016/s0893-133x(96)00278-3 · Cited by 50
CRHCeA→VTA inputs inhibit the positive ensembles to induce negative effect of opiate withdrawal
Jiang, C., Yang, X., He, G., Wang, Z., Wang, Z., Xu, W., Ma, L., Ma, L., & Wang, F. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01321-9 · Cited by 49
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Drug withdrawal conceptualized as a stressor
Chartoff, E. H., & Carlezon, W. A. (2014) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000080 · Cited by 44
“For example, corticosterone facilitates dopamine effects and potentiates drug reward (Piazza et al., 1993), and CRF injected into the VTA stimulates dopamine neurons (Kalivas et al., 1987).”
BackgroundKorzan, W. J., & Summers, C. H. (2007) · Brain Behavior and Evolution · doi:10.1159/000105489 · Cited by 45
“Stress coping is further connected to this output as the stress-related neuropeptide corticotropin releasing factor delivered to the ventral tegmental area has been demonstrated to increase stereotypical locomotory output [Kalivas et al., 1987].”
BackgroundErb, S. M., Funk, D. R., & Lê, A. D. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1556-1 · Cited by 45
“Both areas contain CRF receptors, and CRF infusions into either area increase motoric activity (Holahan et al. 1997; Kalivas et al. 1987).”
BackgroundSu, J., Tanaka, Y., Muratsubaki, T., Kano, M., Kanazawa, M., & Fukudo, S. (2014) · Neurogastroenterology & Motility · doi:10.1111/nmo.12462 · Cited by 45
Pucci, M., Bonaventura, M. V. M. D., Giusepponi, M. E., Romano, A., Filaferro, M., Maccarrone, M., Ciccocioppo, R., Cifani, C., & D’Addario, C. (2015) · Addiction Biology · doi:10.1111/adb.12303 · Cited by 42
“Of interest was the consistent increase between the gene expression changes and the levels of both CRF and CRF-1R in the VTA of rats showing binge-eating behavior, whereas no alterations where found in the hypothalamus (Figure S3).”
BackgroundInfluentialBoadle‐Biber, M. C., Singh, V. B., Corley, K. C., Phan, T.-H., & Dilts, R. P. (1993) · Brain Research · doi:10.1016/0006-8993(93)90944-i · Cited by 40
Corticotropin releasing factor and neuroplasticity in cocaine addiction
Corominas, M., Roncero, C., & Casas, M. (2009) · Life Sciences · doi:10.1016/j.lfs.2009.11.005 · Cited by 39
“…effectors of stress, corticotropin releasing factor (CRF), facilitates addiction by increasing locomotion (Cador et al. 1992, 1993; Erb et al. 2003; Kalivas et al. 1987), mediating the response to conditioned stimuli (Lu et al. 2001), and facilitating relapse during abstinence (Erb et al. 1998;…”
InfluentialHarro, J., Tõnissaar, M., & Eller, M. (2001) · Neuropeptides · doi:10.1054/npep.2001.0851 · Cited by 42
Esparza, M. A., Bollati, F. A., García‐Keller, C., Virgolini, M. B., Lopez, L. M., Brusco, A., Shen, H., Kalivas, P. W., & Cancela, L. M. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08239.x · Cited by 36
“…within the ventral tegmental area (VTA; Tagliaferro & Morales, 2008), and injection of CRF directly into the VTA increases locomotor activity (Kalivas et al., 1987), while injection of CRF antagonists inhibits stress-induced reinstatement of cocaine-seeking (Wang et al., 2005, 2007) as well…”
BackgroundGoeders, N. E., & Guerin, G. F. (2008) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2008.07.005 · Cited by 35
“Accordingly, the administration of CRF directly into the VTA results in a time-dependent decrease in prefrontal cortical dopamine metabolism with an increase in dopamine turnover in the nucleus accumbens (Kalivas et al., 1987).”
Cholecystokinin Modulation of Mesolimbic Dopamine Function: Regulation of Motivated Behaviour
Rotzinger, S., Bush, D. E. A., & Vaccarino, F. J. (2002) · Pharmacology & Toxicology · doi:10.1034/j.1600-0773.2002.910620.x · Cited by 33
The neuroanatomic complexity of the CRF and DA systems and their interface: What we still don’t know
Kelly, E. A., & Fudge, J. L. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.04.014 · Cited by 31
Knapp, D. J., Overstreet, D. H., Huang, M. M., Wills, T. A., Whitman, B. A., Angel, R. A., Sinnett, S. E., & Breese, G. R. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2366-5 · Cited by 32
“Likewise, local injection of CRF into the Amyg, DRN, or VTA can also have an acute activating action (Hiroi and Neumaier 2009; Kalivas et al. 1987; Lack et al. 2008; Lee and Tsai 1989; Meloni et al. 2008; Wand 2005).”
BackgroundAyesta, F. J. A., & Nikolarakis, K. E. (1989) · Brain Research · doi:10.1016/0006-8993(89)91667-3 · Cited by 31
Bryce, C. A., & Floresco, S. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05244-w · Cited by 29
Escalated cocaine “binges” in rats: enduring effects of social defeat stress or intra-VTA CRF
Leonard, M. Z., DeBold, J. F., & Miczek, K. A. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4677-7 · Cited by 28
“CRF doses were selected based on previous in vivo studies in rats (Kalivas et al. 1987; Blacktop et al. 2011; Wanat et al. 2013).”
MethodErb, S. M., Kayyali, H., & Romero, K. (2006) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2006.08.002 · Cited by 28
Yang, H., Li, W. P., Reeve, J. R., Rivier, J., & Taché, Y. (1998) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0701767 · Cited by 28
“…receptor proteins has been carried out (Bard et al., 1995; Nakamura et al., 1995; Gehlert et al., 1996a,b; Gerald et al., 1996; Gregor et al., 1996a,b; Hu et al., 1996; Weinberg et al., 1996) except for the Y3 and PYY-preferring receptor (Kalivas et al., 1987; Mannon et al., 1993; Gehlert, 1994).”
BackgroundPleil, K. E., & Skelly, M. J. (2018) · Alcohol · doi:10.1016/j.alcohol.2018.01.007 · Cited by 29
Austin, M. C. (1997) · Neuropsychopharmacology · doi:10.1016/s0893-133x(97)00083-3 · Cited by 27
Social interaction reward in rats has anti‐stress effects
Lemos, C., Salti, A., Amaral, I. M., Fontebasso, V., Singewald, N., Dechant, G., Hofer, A., & Rawas, R. E. (2020) · Addiction Biology · doi:10.1111/adb.12878 · Cited by 26
“Human/rat CRF, alpha-helical CRF (9-41), and SB203580 were”
Low doses of corticotropin-releasing factor potentiate amphetamine-induced stereotyped behavior
Cole, B. J., & Koob, G. F. (1989) · Psychopharmacology · doi:10.1007/bf00634448 · Cited by 26
Boehm, S. L., Reed, C. L., McKinnon, C. S., & Phillips, T. J. (2002) · Psychopharmacology · doi:10.1007/s00213-002-1000-y · Cited by 26
Molecular Signaling and Translational Significance of the Corticotropin Releasing Factor System
Ronan, P. J., & Summers, C. H. (2011) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-385506-0.00006-5 · Cited by 24
Conti, L. H., Costill, J. E., Flynn, S. P., & Tayler, J. E. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.4.1052 · Cited by 25
Fluoxetine inhibits corticotropin-releasing factor (CRF)-induced behavioural responses in rats
Lowry, C. A., Lowry, C. A., Hale, M. W., Lowry, C. A., Hale, M. W., Plant, A., Windle, R. J., Lowry, C. A., Hale, M. W., Plant, A., et al. (2008) · Stress · doi:10.1080/10253890802309861 · Cited by 25
“…and noradrenergic systems may contribute to CRF-induced behavioural arousal, elegant work has established that CRF-induced motor activation is not dependent upon activation of mesolimbic dopaminergic systems (Koob et al. 1984; Swerdlow and Koob 1985; Swerdlow et al. 1986; Kalivas et al. 1987).”
BackgroundVranjkovic, O., Newenhizen, E. C. V., Nordness, M. E., Blacktop, J. M., Urbanik, L. A., Mathy, J. C., McReynolds, J. R., Miller, A. M., Doncheck, E. M., Kloehn, T. M., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2080-18.2018 · Cited by 26
“Although studies examining the regulation of mesocortical dopamine by VTA CRF have produced mixed results (Kalivas et al., 1987), reports that intracerebroventricular CRF increases dopaminergic neurotransmission in the prefrontal cortex (Dunn and Berridge, 1987; Lavicky and Dunn, 1993) and that CRF…”
ResultStudies on the interaction between ICV effects of CRF and CNS noradrenaline depletion
Bakke, H. K., Bogsnes, A., & Murison, R. C. C. (1990) · Physiology & Behavior · doi:10.1016/0031-9384(90)90379-i · Cited by 23
Murphy, E., Sved, A. F., & Finlay, J. M. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00565-1 · Cited by 23
Kalló, I., Molnár, C. S., Szöke, S., Fekete, C., Hrabovszky, E., & Liposits, Z. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00112 · Cited by 21
“, 1989), in the NAc shell (Kalivas et al., 1987) and in the basolateral amygdala (Inglis and Moghaddam, 1999).”
BackgroundAmir, S., & Stewart, J. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.04.003 · Cited by 21
Sharkey, J., Appel, N. M., & Souza, E. B. D. (1989) · Synapse · doi:10.1002/syn.890040109 · Cited by 21
“In support of the latter hypothesis, CRF administration has been reported to alter dopamine turnover in nucleus accumbens and prefrontal cortex (Dunn and Berridge, 1985; Kalivas et al., 1987) and has been shown to increase the firing rate of noradrenergic neurons in locus coeruleus (Valentino et al.”
BackgroundErb, S. M., & Brown, Z. J. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.05.024 · Cited by 20
Metadata
- Authors
- Kalivas, P. W., Duffy, P., & Latimer, L. G.
- Affiliations
- Washington State University (US)
- ORCID
- Kalivas, P W
- Venue
- The Journal of Pharmacology and Experimental Therapeutics
- Publisher
- Elsevier BV
- Published
- 1987-09
- Volume
- 242
- Issue
- 3
- Pages
- 757-763
- ISSN
- 0022-3565 (ISSN-L)
- OpenAlex
- W2272340543
- Cited by
- 137
- References
- 0
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 1 · 2022: 3 · 2021: 1 · 2020: 1 · 2019: 1 · 2018: 5 · 2017: 3 · 2016: 3 · 2015: 6 · 2014: 6 · 2013: 4 · 2012: 6
- FWCI
- 1.39
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Pharmacology and Experimental Therapeutics (publishedVersion)
- PubMed (publishedVersion)
- PubMed
- Funders
- National Institute of Mental Health (MH-40817)
- National Institute on Drug Abuse (DA03906)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- corticotropin-releasing factor, ventral tegmental area, dopamine metabolism, mesolimbic dopamine system, mesocortical dopamine system, motor stimulation, prefrontal cortex, nucleus accumbens, stress, haloperidol, intraventricular injection
- MeSH terms
- Animals, Corticotropin-Releasing Hormone, Dopamine, Dose-Response Relationship, Drug, Frontal Lobe, Haloperidol, Male, Motor Activity, Naloxone, Rats, Inbred Strains, Tegmentum Mesencephali, Rats
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