The DOI matches its Crossref record; 63 of the 63 references it cites were found in a registry or an index.
Increased dopamine and norepinephrine release in medial prefrontal cortex induced by acute and chronic stress: Effects of diazepam
Abstract
We have examined the effects of diazepam on the stress-induced increase in extracellular dopamine and norepinephrine in the medial prefrontal cortex using in vivo microdialysis. In naive rats, acute tail pressure (30 min) elicited an increase in the concentrations of dopamine and norepinephrine in extracellular fluid of medial prefrontal cortex (+54 and +50%, respectively). Diazepam (2.5 mg/kg, i.p.) decreased the basal concentration of extracellular dopamine and norepinephrine. Diazepam also attenuated the stress-evoked increase in the absolute concentrations of extracellular dopamine (+17%), but did not alter the stress-induced increase in norepinephrine (+41%). However, when the drug-induced decrease in basal dopamine and norepinephrine concentration was taken into account, the stress-induced net increase in dopamine above the new baseline was equivalent to that obtained in vehicle pretreated rats, whereas the net increase in norepinephrine was almost twice that obtained in control subjects. In rats previously exposed to chronic cold (three to four weeks at 5 degrees C), tail pressure again produced an increase in the concentrations of dopamine and norepinephrine in the medial prefrontal cortex (+42% and +92%, respectively). However, in these chronically stressed rats, diazepam no longer decreased basal dopamine or norepinephrine in extracellular fluid, nor did it affect the stress-induced increase in the concentrations of these catecholamines. These data indicate that diazepam has complex effects on the extracellular concentrations of dopamine and norepinephrine which vary depending upon whether the rat is undisturbed or stressed during the period of drug exposure as well as the rat's prior history of exposure to stress. Moreover, these data raise questions regarding the role of catecholamines in the mechanism by which diazepam exerts its anxiolytic properties.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Under stressful conditions, there are high levels of catecholamine release in PFC (Deutch and Roth, 1990; Finlay et al., 1995)”
From Catecholamine influences on prefrontal cortical function: Relevance to treatment of attention deficit/hyperactivity disorder and related disorders (2011) · cites this paper as Finlay et al., 1995
In the citing paper
“Biochemical studies in rats have consistently shown that both DA and NA release are increased in the medial PFC during acute stress exposure (30–32).”
From Catecholamine Influences on Dorsolateral Prefrontal Cortical Networks (2011) · cites this paper as [32]
In the citing paper
“However, under conditions of uncontrollable stress, there are high levels of NE and DA release in the PFC (Finlay et al., 1995, Murphy et al., 1996), which engage α1-AR and D1R to drive Ca2+-PKC and cAMP-PKA signaling, rapidly opening nearby K+ channels to weaken PFC network connectivity and impair working memory and top-down control (Fig. 4B); (Arnsten et al., 2019, Birnbaum et al., 2004, Gamo et”
From Guanfacine’s mechanism of action in treating prefrontal cortical disorders: Successful translation across species (2020) · cites this paper as Finlay et al., 1995
Citations
Cites
The rat brain in stereotaxic coordinates
Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
Abercrombie, E. D., Keefe, K. A., DiFrischia, D. S., & Zigmond, M. J. (1989) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1989.tb09224.x · Cited by 1,106
Self-citationA simple and reliable conflict procedure for testing anti-anxiety agents
Vogel, J. R., Beer, B., & Clody, D. E. (1971) · Psychopharmacology · doi:10.1007/bf00403989 · Cited by 851
Carboni, E., Tanda, G., Frau, R., & Chiara, G. D. (1990) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1990.tb04599.x · Cited by 412
Radiohistochemical localization of benzodiazepine receptors in rat brain.
Young, W. S., & Kuhar, M. J. (1980) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)31961-0 · Cited by 390
Microdialysis in the Neurosciences
(1991) · Techniques in the behavioral and neural sciences · doi:10.1016/c2013-0-04455-6 · Cited by 348
Abercrombie, E., Keller, R., & Zigmond, M. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90192-3 · Cited by 342
Self-citationRegional and laminar density of the dopamine innervation in adult rat cerebral cortex
Descarries, L., Lemay, B., Doucet, G., & Berger, B. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90038-8 · Cited by 341
Lavielle, S., Tassin, J., Thierry, A. M., Blanc, G., Hervé, D., Barthélémy, C., & Glowinski, J. (1979) · Brain Research · doi:10.1016/0006-8993(79)90311-1 · Cited by 328
Cited by
Sorted by citations
Items 201–300 of 433
Potential Noradrenergic Targets for Cognitive Enhancement in Schizophrenia
Friedman, J. I., Stewart, D. G., & Gorman, J. M. (2004) · CNS Spectrums · doi:10.1017/s1092852900009330 · Cited by 39
Effects of acupuncture on stress-induced relapse to cocaine-seeking in rats
Yoon, S. S., Yang, E. J., Lee, B. H., Jang, E. Y., Kim, H. Y., Choi, S., Steffensen, S. C., & Yang, C. H. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2683-3 · Cited by 40
Devilbiss, D. M., Jenison, R. L., & Berridge, C. W. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002681 · Cited by 40
Sher, L., Oquendo, M. A., Li, S., Burke, A. K., Grunebaum, M. F., Zalsman, G., Huang, Y., & Mann, J. J. (2004) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2004.09.009 · Cited by 40
Physiological and behavioural responsivity to stress and anxiogenic stimuli in COMT-deficient mice
Desbonnet, L., Tighe, O., Karayiorgou, M., Gogos, J. A., Waddington, J. L., & O’Tuathaigh, C. M. P. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.12.014 · Cited by 38
Zhang, Q., Yu, Y.-P., Ye, Y., Zhang, J.-T., Zhang, W., & Wei, E.-Q. (2010) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2010.09.011 · Cited by 38
Tyrosine improves behavioral and neurochemical deficits caused by cold exposure
Yeghiayan, S. K., Luo, S., Shukitt‐Hale, B., & Lieberman, H. R. (2001) · Physiology & Behavior · doi:10.1016/s0031-9384(00)00398-x · Cited by 37
Schelp, S. A., Brodnik, Z. D., Rakowski, D. R., Pultorak, K. J., Sambells, A. T., España, R. A., & Oleson, E. B. (2017) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.117.241802 · Cited by 37
Catechol-O-Methyltransferase moderates effect of stress mindset on affect and cognition
Crum, A. J., Akinola, M., Turnwald, B. P., Kaptchuk, T. J., & Hall, K. T. (2018) · PLoS ONE · doi:10.1371/journal.pone.0195883 · Cited by 37
Prakash, P., Merali, Z., Kolajova, M., Tannenbaum, B. M., & Anisman, H. (2006) · Brain Research · doi:10.1016/j.brainres.2006.06.089 · Cited by 39
Hernaus, D., & Mehta, M. A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.06.057 · Cited by 36
Slavova, D., Ortiz, V., Blaise, M., Bairachnaya, M., Giros, B., & Isingrini, E. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105925 · Cited by 40
From vice to virtue: Insights from sensitization in the nonhuman primate
Castner, S. A., & Williams, G. V. (2007) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2007.08.026 · Cited by 35
Blockade of the mGlu5 receptor decreases basal and stress-induced cortical norepinephrine in rodents
Page, M., Szeliga, P., Gasparini, F., & Cryan, J. (2005) · Psychopharmacology · doi:10.1007/s00213-005-2142-5 · Cited by 34
Demin, K. A., Kolesnikova, T. O., Galstyan, D. S., Krotova, N. A., Ilyin, N. P., Derzhavina, K. A., Levchenko, N. A., Strekalova, T. V., de Abreu, M. S., Petersen, E. V., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-92422-6 · Cited by 33
Noguchi, T., Yoshida, Y., & Chiba, S. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02868-2 · Cited by 32
Monoamine receptors in the prefrontal cortex of Tupaia belangeri during chronic psychosocial stress
Flügge, G., Ahrens, O., & Fuchs, E. (1997) · Cell and Tissue Research · doi:10.1007/s004410050787 · Cited by 31
Ameliorating effects of gypenosides on chronic stress-induced anxiety disorders in mice
Zhao, T., Shin, K. S., Choi, H. S., & Lee, M. K. (2015) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-015-0856-4 · Cited by 30
Arnsten, A. F. T. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1274-9 · Cited by 32
Unstable Maternal Environment Affects Stress Response in Adult Mice in a Genotype-Dependent Manner
Segni, M. D., Andolina, D., Luchetti, A., Babicola, L., D'Apolito, L. I., Pascucci, T., Conversi, D., Accoto, A., D'Amato, F. R., & Ventura, R. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv204 · Cited by 31
Section III. The Norepinephrine System
Smythies, J. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)64003-2 · Cited by 30
Beaufour, C., Bihan, C. L., Hamon, M., & Thiébot, M.-H. (2001) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(01)00492-0 · Cited by 30
O’Daly, O., Joyce, D. W., Stephan, K. E., Murray, R. M., & Shergill, S. S. (2011) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2011.3 · Cited by 29
Yuen, E. Y., Wei, J., & Yan, Z. (2017) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyx052 · Cited by 31
Allopregnanolone Decreases Evoked Dopamine Release Differently in Rats by Sex and Estrous Stage
Dornellas, A. P. S., Macedo, G. C., McFarland, M. H., Gómez‐A, A., O’Buckley, T. K., Cunha, C. D., Morrow, A. L., & Robinson, D. L. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.608887 · Cited by 29
Noradrenergic contributions to cue-driven risk-taking and impulsivity
Chernoff, C. S., Hynes, T. J., & Winstanley, C. A. (2021) · Psychopharmacology · doi:10.1007/s00213-021-05806-x · Cited by 32
Yu, Z., Yi, X., Wang, Y., Zeng, G., Tan, C., Cheng, Y., Sun, P., Liu, Z., Wang, Y., & Liu, Y. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15603 · Cited by 26
Leggio, G. M., Micale, V., Foll, B. L., Mazzola, C., Nóbrega, J. N., & Drago, F. (2010) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2010.05.006 · Cited by 29
Regional Cerebral Blood Flow in Schizophrenia and the Local Circuit Neurons Hypothesis
Bachneff, S. A. (1996) · Schizophrenia Bulletin · doi:10.1093/schbul/22.1.163 · Cited by 30
Arnsten, A. F. T., Ishizawa, Y., & Xie, Z. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02057-4 · Cited by 30
Dopaminergic Reward Pathways and Effects of Stress
Marinelli, M. (2007) · Elsevier eBooks · doi:10.1016/b978-012370632-4/50006-1 · Cited by 30
Noradrenergic fiber sprouting and altered transduction in neuropathic prefrontal cortex
Matos, S. C., Zamfir, M., Longo, G., Ribeiro‐da‐Silva, A., & Séguéla, P. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1543-7 · Cited by 28
Modulation of plus-maze behaviour in mice by the preferential D3-receptor agonist 7-OH-DPAT
Rodgers, R. J., Johnson, N. J., Champion, A. J., & Mills, S. (1996) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(95)02110-8 · Cited by 28
Venator, D. K., Lewis, D. A., & Finlay, J. M. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00131-1 · Cited by 28
Self-citationScientific Rationale for the Treatment of Cognitive Deficits from Long COVID
Zadeh, A. F., Arnsten, A. F. T., & Wang, M. (2023) · Neurology International · doi:10.3390/neurolint15020045 · Cited by 27
Bremner, J. D. (2007) · Cambridge University Press eBooks · doi:10.1017/cbo9780511500008.010 · Cited by 28
Rogóż, Z., Skuza, G., & Kłlodzińska, A. (2004) · PubMed · Cited by 27
Fry, A. C., Steinacker, J. M., & MEEUSEN, R. R. (2005) · doi:10.1002/9780470757826.ch37 · Cited by 27
Tsai, Y.-J., Hsieh, S., Huang, C., & Hung, T. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.617596 · Cited by 32
Jung, M., Ryu, S., Kang, M., Javadi, A., & Loprinzi, P. D. (2021) · Quarterly Journal of Experimental Psychology · doi:10.1177/17470218211048807 · Cited by 30
Fitzgerald, P. J. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.04.003 · Cited by 29
Tjurmina, O., Goldstein, D. S., Palkovits, M., & Kopin, I. J. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01281-0 · Cited by 27
The impact of stress on social behavior in adult zebrafish (Danio rerio)
Saszik, S. M., & Smith, C. M. (2017) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000338 · Cited by 26
NicNiocaill, B., & Gratton, A. P. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0723-1 · Cited by 25
Romaniuk, A., Koprowska, M., Krotewicz, M., Strzelczuk, M., & Wieczorek, M. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00357-0 · Cited by 25
Zucker, M., Weizman, A., & Rehavi, M. (2004) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2004.08.009 · Cited by 25
Dalley, J. W., Mason, K., & Stanford, S. C. (1996) · Psychopharmacology · doi:10.1007/bf02805974 · Cited by 25
Wang, C., Li, M., Sawmiller, D. R., Fan, Y., Ma, Y., Tan, J., Ren, Y., & Li, S. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.11.028 · Cited by 24
Noradrenergic Source of Dopamine Assessed by Microdialysis in the Medial Prefrontal Cortex
Devoto, P., Sagheddu, C., Santoni, M., Flore, G., Saba, P., Pistis, M., & Gessa, G. L. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.588160 · Cited by 24
Cryan, J. F., & Dev, K. K. (2008) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(07)00013-6 · Cited by 25
Disruption of cortical-limbic interaction as a substrate for comorbidity
Grace, A. A. (2006) · Neurotoxicity Research · doi:10.1007/bf03033238 · Cited by 24
Gómez‐A, A., Fiorenza, A. M., Boschen, S. L., Sugi, A. H., Beckman, D., Ferreira, S. T., Lee, K., Blaha, C. D., & Cunha, C. D. (2016) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00358 · Cited by 23
Bavley, C. C., Fetcho, R. N., Burgdorf, C. E., Walsh, A. P., Fischer, D. K., Hall, B. S., Sayles, N. M., Contoreggi, N. H., Hackett, J. E., Antigua, S. A., et al. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0513-2 · Cited by 23
Dopaminergic mechanisms underlying catalepsy, fear and anxiety: Do they interact?
Colombo, A. C., de Oliveira, A. R., Reimer, A. E., & Brandão, M. L. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.10.002 · Cited by 23
Epinephrine modulation of memory: Amygdala activation and regulation of long-term memory storage.
Liang, K. (2001) · American Psychological Association eBooks · doi:10.1037/10413-009 · Cited by 23
Murphy, E., Sved, A. F., & Finlay, J. M. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00565-1 · Cited by 23
Self-citationDefining the interconnectivity of the medial prefrontal cortex and ventral midbrain
Hui, M., & Beier, K. T. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.971349 · Cited by 25
Elevated Anxiety and Impaired Attention in Super-Smeller, Kv1.3 Knockout Mice
Huang, Z., Hoffman, C. A., Chelette, B. M., Thiebaud, N., & Fadool, D. A. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00049 · Cited by 20
Guanfacine ameliorates hypobaric hypoxia induced spatial working memory deficits
Kauser, H., Sahu, S., Kumar, S., & Panjwani, U. (2013) · Physiology & Behavior · doi:10.1016/j.physbeh.2013.10.028 · Cited by 22
Lustberg, D. J., Liu, J. Q., Iannitelli, A. F., Vanderhoof, S. O., Liles, L. C., McCann, K. E., & Weinshenker, D. (2022) · Hormones and Behavior · doi:10.1016/j.yhbeh.2022.105205 · Cited by 21
Wei, L., Zhu, Y.-M., Zhang, Y., Liang, F., Jia, H., Qu, C., Wang, J., Tang, J., Lu, S., Huo, F., et al. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.06.006 · Cited by 21
Rigid Analogues of the α2-Adrenergic Blocker Atipamezole: Small Changes, Big Consequences
Vacher, B., Funes, P., Chopin, P., Cussac, D., Heusler, P., Tourette, A., & Marien, M. R. (2010) · Journal of Medicinal Chemistry · doi:10.1021/jm1006269 · Cited by 21
Chattopadhyay, N., Singh, D. P., Heese, O., Godbole, M. M., Shinohara, T., Black, P. M., & Brown, E. M. (2000) · Journal of Neuroscience Research · doi:10.1002/1097-4547(20000701)61:1 · Cited by 103
Neurotransmitter, neurohormonal, and neuropeptidal function in stress and PTSD
Bremner, J. D., & Pearce, B. R. (2016) · Wiley eBooks · doi:10.1002/9781118356142.ch9 · Cited by 22
Calefi, A. S., Fonseca, J. G. D. S., Nunes, C. A. D. Q., Lima, A. P., Quinteiro-Filho, W. M., Flório, J. C., Zager, A., Ferreira, A. J. P., & Palermo‐Neto, J. (2019) · Veterinary Sciences · doi:10.3390/vetsci6010004 · Cited by 20
Autophagy status as a gateway for stress-induced catecholamine interplay in neurodegeneration
Fornai, F., & Puglisi‐Allegra, S. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.01.015 · Cited by 20
Lorrain, D. S., Baccei, C. S., Correa, L. D., & Bristow, L. J. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.12.022 · Cited by 20
B��que, J.-C., de Montigny, C., Blier, P., & Debonnel, G. (1999) · Synapse · doi:10.1002/(sici)1098-2396(19990601)32:3 · Cited by 69
Dietz, A. G., Weikop, P., Hauglund, N. L., Andersen, M., Petersen, N., Rose, L., Hirase, H., & Nedergaard, M. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2305071120 · Cited by 18
Kiyatkin, E. A., & Bae, D. D. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0965-y · Cited by 19
Neurochemical and behavioral effects of chronic unpredictable stress
Matuszewich, L., McFadden, L. M., Friedman, R. D., & Frye, C. A. (2014) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000061 · Cited by 18
Warner, T. A., & Drugan, R. C. (2011) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.11.009 · Cited by 18
Steciuk, M., Kram, M., Kramer, G. L., & Petty, F. (2000) · Stress · doi:10.3109/10253890009001123 · Cited by 18
Chronic cold stress regulates ascending noradrenergic pathways
Featherby, T. J., & Lawrence, A. J. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.06.019 · Cited by 18
NMDAR Neurotransmission Needed for Persistent Neuronal Firing: Potential Roles in Mental Disorders
Yang, S., Seo, H., Wang, M., & Arnsten, A. F. T. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.654322 · Cited by 17
Overtraining and the Central Nervous System
MEEUSEN, R. R. (2007) · Springer eBooks · doi:10.1007/978-0-585-34048-7_15 · Cited by 17
Quetiapine ameliorates stress-induced cognitive inflexibility in rats
Nikiforuk, A. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.06.042 · Cited by 15
Reduction of prelimbic inhibitory gating of auditory evoked potentials after fear conditioning.
Mears, R. P., Boutros, N. N., & Cromwell, H. C. (2009) · Behavioral Neuroscience · doi:10.1037/a0014364 · Cited by 15
Panhelainen, A. E., Vekovischeva, O. Y., Aitta‐aho, T., Rasanen, I., Ojanperä, I. A., & Korpi, E. R. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.07.004 · Cited by 16
Di, G., Zhou, B. Y., Li, Z., & Lin, Q. (2011) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b1000439 · Cited by 16
Lamb, Y. N., Thompson, J., Murphy, R., Wall, C. R., Kirk, I. J., Morgan, A. R., Ferguson, L. R., Mitchell, E. A., & Waldie, K. E. (2014) · Cognition · doi:10.1016/j.cognition.2014.05.009 · Cited by 18
Nanni, G., Scheggi, S., Leggio, B., Grappi, S., Masi, F., Rauggi, R., & Montis, M. G. D. (2003) · Journal of Neuroscience Research · doi:10.1002/jnr.10685 · Cited by 16
García‐Vallejo, P., Gómez, F. M., Infante, C., Ginestal, E., & Giralt, M. T. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00547-2 · Cited by 16
Hernaus, D., Quaedflieg, C. W. E. M., Offermann, J. S., Santa, M. M. C., & van Amelsvoort, T. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx122 · Cited by 15
The Locus Coeruleus-Noradrenergic System and Stress: Implications for Post-Traumatic Stress Disorder
Berridge, C. W. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-329-9_10 · Cited by 15
Recent Progress in Some Aircraft Technologies
Agarwal, R. K. (2016) · InTech eBooks · doi:10.5772/61381 · Cited by 15
Koprowska, M., Krotewicz, M., Romaniuk, A., Strzelczuk, M., & Wieczorek, M. (1999) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-1999-1291 · Cited by 15
Satoh, H., Suzuki, H., & Saitow, F. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.10.039 · Cited by 14
Chronic Restraint Stress Affects Network Oscillations in the Anterior Cingulate Cortex in Mice
Ito, R., Nakano, T., Hojo, Y., Hashizume, M., Koshiba, M., & Murakoshi, T. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.04.021 · Cited by 14
Koga, Y., Higashi, S., Kawahara, H., & Ohsumi, T. (2007) · The Journal of the Kyushu Dental Society · doi:10.2504/kds.61.39 · Cited by 14
Yoshitake, S., Ijiri, S., Kehr, J., & Yoshitake, T. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.12.011 · Cited by 14
Mania: a Rational Neurobiology
Arnsten, A., & Manji, H. (2008) · Future Neurology · doi:10.2217/14796708.3.2.125 · Cited by 14
Jeong, J., Kim, D. K., Chung, S., Han, J. W., Han, J., & Mook‐Jung, I. (2024) · Aging Cell · doi:10.1111/acel.14420 · Cited by 14
Nielsen, D. M., Crosley, K. J., Keller, R. W., Glick, S. D., & Carlson, J. N. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01129-4 · Cited by 13
Role of prefrontal cortex in stress responsivity
Gratton, A. P., & Sullivan, R. M. (2005) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(05)80043-4 · Cited by 13
Vilkman, H., Kajander, J., Aalto, S., Vahlberg, T. J., Någren, K., Allonen, T., Syvälahti, E. K. G., & Hietala, J. A. (2009) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2009.04.006 · Cited by 13
Piri, M., Ayazi, E., & Zarrindast, M. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.07.009 · Cited by 12
Joyce, M. K. P., Ivanov, T. G., Krienen, F. M., Mitchell, J. F., Ma, S., Inoue, W., Nandy, A. S., Datta, D., Duque, A., Arellano, J. I., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-08297-0 · Cited by 13
Fedotova, J. (2013) · Acta Physiologica Hungarica · doi:10.1556/aphysiol.100.2013.2.8 · Cited by 11
Nisar, R., Batool, Z., & Haider, S. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121707 · Cited by 11
Metadata
- Authors
- Finlay, J. M., Zigmond, M. J., & Abercrombie, E. D.
- Affiliations
- University of Pittsburgh (US)
- Corresponding author
- Finlay, J.M.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 1995-02
- Volume
- 64
- Issue
- 3
- Pages
- 619-628
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W2033146497
- Cited by
- 434
- References
- 63
- Citations by year
- 2026: 3 · 2025: 9 · 2024: 10 · 2023: 17 · 2022: 8 · 2021: 12 · 2020: 10 · 2019: 17 · 2018: 16 · 2017: 17 · 2016: 16 · 2015: 15 · 2014: 22 · 2013: 15 · 2012: 16
- FWCI
- 3.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Rutgers University Community Repository (Rutgers University) (submittedVersion)
- Funders
- National Institutes of Health (5r01mh043947-02)
- National Institute of Mental Health (MH 43947, MH 45156, MH 00058, P50MH045156)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- diazepam, acute stress, chronic stress, medial prefrontal cortex, dopamine, norepinephrine, anxiolytic mechanism, cold stress
- MeSH terms
- Animals, Cold Temperature, Diazepam, Dopamine, Dose-Response Relationship, Drug, Homovanillic Acid, Male, Norepinephrine, Nucleus Accumbens, Receptors, GABA-A, Stress, Physiological, Time Factors, 3,4-Dihydroxyphenylacetic Acid, Rats, Sprague-Dawley, Prefrontal Cortex, Microdialysis, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review