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Chapter 9 - The Sensitivity and Vulnerability of the Prefrontal Cortex to Changes in Daily Rhythms

Published online by Cambridge University Press:  05 January 2019

Michael W. Hoffmann
Michael W. Hoffmann
Affiliation:
University of Central Florida
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Assembly of the Executive Mind
Evolutionary Insights and a Paradigm for Brain Health
 , pp. 144 - 153
Publisher: Cambridge University Press
Print publication year: 2019

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References

Broadbent, D. Decision and Stress. Academic, London, 1971.Google Scholar
Hockey, GRJ. Effect of loud noise on attentional selectivity. Q J Exp Psychol 1970; 22: 28–36.Google Scholar
Goldman-Rakic, PS. Circuitry of primate prefrontal cortex and regulation of behavior by representational memory. In: Plum, F (ed.), Handbook of Physiology, The Nervous System, Higher Functions of the Brain vol. V. American Physiological Society, Bethesda, MD, 1987.Google Scholar
Price, JL, Amaral, DG. An autoradiographic study of the projections of the central nucleus of the monkey amygdala. J Neurosci 1981; 1: 1242–1259.CrossRefGoogle ScholarPubMed
Price, JL, Carmichael, ST, Drevets, WC. Networks related to the orbital and medial prefrontal cortex: a substrate for emotional behavior? Brain Res 1996; 107: 523–536.CrossRefGoogle Scholar
Ghashghaei, HT, Barbas, H. Pathways for emotion: interactions of prefrontal and anterior temporal pathways in the amygdala of the rhesus monkey. Neuroscience 2002; 115: 1261–1279.CrossRefGoogle ScholarPubMed
Debiec, J, LeDoux, JE. Noradrenergic signaling in the amygdala contributes to the reconsolidation of fear memory: treatment implications for PTSD. Ann NY Acad Sci 2006; 1071: 521–524.CrossRefGoogle Scholar
Kojima, S, Goldman-Rakic, PS. Delay-related activity of prefrontal neurons in rhesus monkeys performing delayed response. Brain Res 1982; 248(1): 43–49.Google Scholar
Robbins, TW, Roberts, AC. Differential regulation of fronto-executive function by the monoamines and acetylcholine. Cerebral Cortex 2007; 17(suppl. 1): i151–i161.Google Scholar
Previc, FH. Dopamine and the origin of human intelligence. Brain Cogn 1999; 41: 299–350.Google Scholar
Bortz, WM II. Physical exercise as an evolutionary force. J Hum Evol 1985; 14: 145–155.Google Scholar
Carrier, DR. The energetic paradox of human running and hominid evolution. Curr Anthropol 1984; 25: 483–495.Google Scholar
Passinghim, RE, Stephan, KE, Kotter, R. The anatomical basis of functional localization in the cortex. Nat Rev Neurosci 2002; 3: 606–616.CrossRefGoogle Scholar
Leonard, WR, Robertson, MS. Comparative primate energetics and hominid evolution. Am J Phys Anthropol 1997; 102: 265–281.3.0.CO;2-X>CrossRefGoogle ScholarPubMed
Lewis, DA, Melchitzky, DS, Sesack, SR, et al. Dopamine transporter immunoreactivity in monkey cerebral cortex: regional, laminar and ultrastructural organization. J Comp Neurol 2001; 432: 119–136.CrossRefGoogle Scholar
Willamson, PC, Allman, JM. The Human Illnesses: Neuropsychiatric Disorders and the Nature of the Human Brain. Oxford University Press, Oxford, 2011.Google Scholar
Sarter, M, Parikh, V. Choline transporters, cholinergic transmission and cognition. Nat Rev Neurosci 2005; 6: 48–56.Google Scholar
Levin, ED, Simon, BB. Nicotinic acetylcholine involvement in cognitive function in animals. Psychopharmacology 1998; 138: 217–230.CrossRefGoogle ScholarPubMed
Jakab, RL, Goldman-Rakic, PS. Segregation of serotonin 5HT 2A and 5HT 3 receptors in inhibitory circuits in the primate cerebral cortex. J Comp Neurol 2000; 417: 337–348.3.0.CO;2-O>CrossRefGoogle Scholar
Soubrie, P. Reconciling the role of central serotonin neurons in human and animal behavior. Behav Brain Sci 1986; 9: 319–364.Google Scholar
McCormick, DA, Pape, HC, Williamson, A. Actions of norepinephrine in the cerebral cortex and thalamus: implications for function of the central noradrenergic system. Prog Brain Res 1991; 88: 293–305.CrossRefGoogle ScholarPubMed
Seamans, JK, Durstewitz, D, Christie, BR, Stevens, CF, Sejnowski, TJ. Dopamine D1/D5 receptor modulation of excitatory synaptic inputs to layer V prefrontal cortex neurons. PNAS 2001; 98: 301–306.CrossRefGoogle Scholar
Arnsten, AFT. Through the looking glass: differential noradrenergic modulation of prefrontal cortical function. Neural Plast 2000; 7: 133–146.CrossRefGoogle Scholar
Arnsten, AFT, Goldman-Rakic, PS. Alpha-2 adrenergic mechanisms in prefrontal cortex associated with cognitive decline in aged nonhuman primates. Science 1985; 230: 1273–1276.Google Scholar
Li, B-M, Mei, Z-T. Delayed response deficit induced by local injection of the alpha-2 adrenergic antagonist yohimbine into the dorsolateral prefrontal cortex in young adult monkeys. Behav Neural Biol 1994; 62: 134–139.CrossRefGoogle ScholarPubMed
Birnbaum, SG, Gobeske, KT, Auerbach, J, Taylor, JR, Arnsten, AFT. A role for norepinephrine in stress-induced cognitive deficits: α-1-adrenoceptor mediation in prefrontal cortex. Biol Psychiatry 1999; 46: 1266–1274.CrossRefGoogle ScholarPubMed
Ramos, BP, Colgan, L, Nou, E, et al. The beta-1 adrenergic antagonist, betaxolol, improves working memory performance in rats and monkeys. Biol Psychiatry 2005; 58: 894–900.CrossRefGoogle ScholarPubMed
Deutch, AY, Roth, RH. The determinants of stress-induced activation of the prefrontal cortical dopamine system. Prog Brain Res 1990; 85: 367–403.CrossRefGoogle ScholarPubMed
Ramos, B, Stark, D, Verduzco, L, van Dyck, CH, Arnsten, AFT. Alpha-2A-adrenoceptor stimulation improves prefrontal cortical regulation of behavior through inhibition of cAMP signaling in aging animals. Learn Mem 2006; 13: 770–776.CrossRefGoogle Scholar
Birnbaum, SG, Yuan, PX, Wang, M, et al. Protein kinase C overactivity impairs prefrontal cortical regulation of working memory. Science 2004; 306: 882–884.Google Scholar
Arnsten, AFT, Mathew, R, Ubriani, R, Taylor, JR, Li, B-M. α-1 noradrenergic receptor stimulation impairs prefrontal cortical cognitive function. Biol Psychiatry 1999; 45: 26–31.Google Scholar
Taylor, F, Raskind, MA. The α1-adrenergic antagonist prazosin improves sleep and nightmares in civilian trauma posttraumatic stress disorder. J Clin Psychopharmacol 2002; 22: 82–85.Google Scholar
Raskind, MA, Thompson, C, Petrie, EC, et al. Prazosin reduces nightmares and other PTSD symptoms in combat veterans: a placebo-controlled study. Am J Psychiatry 2003; 160: 371–373.Google Scholar
Sawaguchi, T, Goldman-Rakic, PS. D1 dopamine receptors in prefrontal cortex: involvement in working memory. Science 1991; 251: 947–950.CrossRefGoogle ScholarPubMed
Zahrt, J, Taylor, JR, Mathew, RG, Arnsten, AFT. Supranormal stimulation of dopamine D1 receptors in the rodent prefrontal cortex impairs spatial working memory performance. J Neurosci 1997; 17: 8528–8535.CrossRefGoogle ScholarPubMed
Vijayraghavan, S, Wang, M, Birnbaum, SG, et al. Inverted-U dopamine D1 receptor actions on prefrontal neurons engaged in working memory. Nature Neurosci 2007; 10: 376–384.CrossRefGoogle ScholarPubMed
Subiaul, F. Mosaic cognitive evolution: the case of imitation behavior. In Broadfield, D, Yuan, M, Schick, K, Toth, N (eds.), The Human Brain Evolving. Stone Age Institute Press, Gosport, IN, 2010.Google Scholar
Walker, SC, Robbins, TW, Roberts, AC. Differential contributions of dopamine and serotonin to orbitofrontal cortex function in the marmoset. Cerebral Cortex 2009; 19: 889–898.CrossRefGoogle ScholarPubMed
Arnsten, AFT, Vijayraghavan, S, Wang, M, et al. Dopamine's influence on prefrontal cortical cognition: actions and circuits in behaving primates. In: Bjorklund, A, Dunnet, S, Iversen, L, Iversen, S (eds.), Dopamine Handbook. Oxford University Press, Oxford, 2009.Google Scholar
Arnsten, AFT. Stress signaling pathways that impair prefrontal cortex structure and function. Nat Rev Neurosci 2009; 32: 267–287.Google Scholar
Arnsten, AFT, Paspalas, CD, Gamo, NJ, et al. Dynamic network connectivity: a new form of neuroplasticity. Trends Cogn Sci 2010; 14: 365–375.CrossRefGoogle ScholarPubMed
Arnsten, AFT. Fleeting thoughts. In: Stuss, DT, Knight, RT (eds.), Principles of Frontal Lobe Function. Oxford University Press, Oxford, 2013.Google Scholar
Hagenston, AM, Fitzpatrick, JS, Yeckel, MF. mGluR-mediated calcium waves that invade the soma regulate firing in layer V medial prefrontal cortical pyramidal neurons. Cereb Cortex 2008; 18: 407–423.Google Scholar
Runyan, JD, Dash, PK. Distinct prefrontal molecular mechanisms for information storage lasting seconds versus minutes. Learn Mem 2005; 12: 232–238.Google Scholar
Partridge, LD, Swandulla, D, Muller, TH. Modulation of calcium-activated non-specific cation currents by cyclic AMP-dependent phosphorylation in neurons of Helix. J Physiol 1990; 429: 131–145.CrossRefGoogle ScholarPubMed
Wang, M, Ramos, BP, Paspalas, CD, et al. α2A-adrenoceptor stimulation strengthens working memory networks by inhibiting cAMP-HCN channel signaling in prefrontal cortex. Cell 2007; 129: 397–410.CrossRefGoogle Scholar
Holmes, A, Wellman, CL. Stress-induced prefrontal reorganization and executive dysfunction in rodents. Neurosci Biobehav Rev 2008. doi: 10.1016/j.neubiorev.2008.11.005.Google Scholar
Radley, JJ, Rocher, AB, Miller, M, et al. Repeated stress induces dendritic spine loss in the rat medial prefrontal cortex. Cereb Cortex 2006; 16: 313–320.CrossRefGoogle ScholarPubMed
Cerqueira, JJ, Mailliet, F, Almeida, OF, Jay, TM, Sousa, N. The prefrontal cortex as a key target of the maladaptive response to stress. J Neurosci 2007; 27: 2781–2787.CrossRefGoogle ScholarPubMed
Radley, JJ, Rocher, AB, Janssen, WG, et al. Reversibility of apical dendritic retraction in the rat medial prefrontal cortex following repeated stress. Exp Neurol 2005; 196: 199–203.Google Scholar
Snijders, C, de Nijs, L, Baker, DG, et al. MicroRNAs in post-traumatic stress disorder. Curr Top Behav Neurosci 2017. doi: 10.1007/7854_2017_32.CrossRefGoogle Scholar
Girgenti, MJ, Duman, RS. Transcriptome alterations in posttraumatic stress disorder. Biol Psychiatry 2017. doi: 10.1016/j.biopsych.2017.09.023.Google ScholarPubMed
Constanzo, ME, Jovanovic, T, Pham, D, et al. White matter microstructure of the uncinate fasciculus is associated with subthreshold posttraumatic stress disorder symptoms and fear potentiated startle during early extinction in recently deployed Service Members. Neurosci Lett 2016; 618: 66–71.CrossRefGoogle Scholar
Papaleo, F, Crawley, JN, Song, J, et al. Genetic dissection of the role of catechol-O-methyltransferase in cognition and stress reactivity in mice. J Neurosci 2008; 28: 8709–8723.Google Scholar
Millar, JK, Pickard, BS, Mackie, S, et al. DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling. Science 2005; 310: 1187–1191.CrossRefGoogle ScholarPubMed

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