Noise stress impairs prefrontal cortical cognitive function in monkeys: Evidence for a hyperdopaminergic mechanism

Archives of General Psychiatry

Volumn 55, Issue 4, 1998, Pages 362-368

  Arnsten, Amy F T ^a   Goldman Rakic, Patricia S ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

8 CHLORO 2,3,4,5 TETRAHYDRO 3 METHYL 5 PHENYL 1H 3 BENZAZEPIN 7 OL HYDROGEN MALEATE; CLONIDINE; DOPAMINE 1 RECEPTOR BLOCKING AGENT; DOPAMINE RECEPTOR BLOCKING AGENT; HALOPERIDOL; NALOXONE;

ANIMAL MODEL; ARTICLE; COGNITION; COGNITIVE DEFECT; CONTROLLED STUDY; DOPAMINERGIC SYSTEM; INTRAMUSCULAR DRUG ADMINISTRATION; MENTAL DISEASE; MONKEY; NOISE; NONHUMAN; PREFRONTAL CORTEX; SPATIAL MEMORY; STRESS; TASK PERFORMANCE; VISUAL DISCRIMINATION;

(R)-2,3,4,5-TETRAHYDRO-8-CHLORO-3-METHYL-5-PHENYL-1H-3-BENZAZEPIN-7-OL; ANIMALS; CLONIDINE; COGNITION DISORDERS; DOPAMINE; FEMALE; HALOPERIDOL; MACACA MULATTA; MALE; MEMORY; NALOXONE; NOISE; PATTERN RECOGNITION, VISUAL; PREFRONTAL CORTEX; RECEPTORS, DOPAMINE; STRESS, PSYCHOLOGICAL;

EID: 0031945083     PISSN: 0003990X     EISSN: None     Source Type: Journal    
DOI: 10.1001/archpsyc.55.4.362     Document Type: Article

References (55)

1. Mazure CM, Does stress cause psychiatric illness? In: Spiegel D, ed, Progress in Psychiatry. Washington. DC: American Psychiatric Press; 1995;46:270.
2. Venault P, Chapoutier G, Prado de Carvalho L, Simiand J, Morre M, Dodd RH, Rossier J. Benzodiazepine impairs and beta-carboline enhances performance in learning and memory tasks. Nature. 1986;321:864-868.
3. McNamara RK, Skelton RW, Benzodiazepine receptor antagonists flumazenil and CGS 8216 and inverse agonist beta-CCM enhance spatial learning in the rat: dissociation from anxiogenic actions, Psychobioiogy. 1993;21:101-108.
4. Holmes PV, Drugan RC. Differential effects of anxiogenic central and peripheral benzodiazepine receptor ligands in tests of learning and memory. Psychopharmacology. 1991;104:249-254.
5. Cahill L, McGaugh JL. Modulation of memory storage. Curr Opin Neurobiol. 1996; 6:237-242.
6. Cahill L, Prins B, Weber M, McGaugh JL. Beta-adrenergic activation and memory for emotional events. Nature. 1994;371:702-704.
7. Broadbent D. Decision and Stress. London, England: Academic Press: 1971.
8. Glass DC, Reim B. Singer JE. Behavioral consequences of adaptation to controllable and uncontrollable noise. J Exp Social Psychol. 1971;7:244-257.
9. Hockey GRJ, Effect of loud noise on attentional selectivity. Q J Exp Psychol. 1970;22:28-36.
10. Hartley LR, Adams RG. Effect of noise on the Stroop test. J Exp Psychol 1974;102:62-66.
11. Wilkins AJ, Shallice T. McCarthy R, Frontal lesions and sustained attention. Neuropsychologia. 1987;25:359-365.
12. Perret E. The left frontal lobe of man and the suppression of habitual responses in verbal categorical behavior. Neuropsychologia. 1974;12:323-330.
13. Thierry AM, Tassin JP, Blanc G, Glowinski J, Selective activation of the mesocortical dopamine system by stress, Nature, 1976;263:242-244.
14. Roth RH, Tam S-Y. Ida Y, Yang J-X, Deutch AY, Stress and the mesocorticollmbic dopamine ystems. Ann N Y Acad Sci. 1988;537:138-147.
15. Abercrombie ED, Keefe KA, DiFrischia DS, Zigmond MJ. Differential effect of stress on in vivo dopamine release in striaturm, nucleus accumbens, and medial frontal cortex. J Neurochem. 1989;52:1655-1658.
16. Kaneyuki H, Yokoo H, Tsuda A, Yoshisa M, Mizuki Y, Yamada M, Tanaka M, Psychological stress increases dopamine turnover selectively in mesoprefrontal dopamine neurons of rats: reversal by diazepam, Brain Res. 1991;557:154-161.
17. Bradberry CW, Lory JD, Roth RH. The anxiogenic beta-carboline FG 7142 selectively increases dopamine release in rat prefrontal cortex as measured by microdiaiysis. J Neurochem. 1991;56:748-752.
18. Deutch AY, Roth RH. The determinants of stress-induced activation of the prefrontal cortical dopamine system. Prog Brain Res, 1990;85:367-403.
19. Grenhoff J, Svensson TH. Clonidlne modulates dopamine cell firing in rat ventral tegmental area. Eur J Pharmacol. 1989;165:11-18.
20. Abhold R, Kalivas PW. Enkephalin release into the ventral tegmental area in response to stress: modulation of mesocorticolimbic dopamine, Brain Res. 1987;414:339-348.
21. Tarn S-Y. Mesoprefrontal Dopamine Neurons: Studies on Their Regulatory Control. New Haven, Conn: Yale University Press: 1986.
22. Murphy BL, Arnsten AFT, Jentsch JD, Roth RH. Dopamine and spatial working memory in rats and monkeys: pharmacological reversal of stress-induced impairment. J Neurosci. 1996;16:7768-7775.
23. Miller JD, Speciale SG, McMillen BA, German DC. Naloxone antagonism of stress-induced augmentation of frontal cortex dopamine metabolism, Eur J Pharmacol. 1984;98:437-439.
24. Brozoski T, Brown RM, Rosvold HE, Goldman PS. Cognitive deficit caused by regional depletion of dopamine in prefrontal cortex of rhesus monkey. Science. 1979;205:929-931.
25. Simon H. Dopaminergic A10 neurons and the frontal system, J Physiol. 1981;77:81-95.
26. Bubser M, Schmidt W. 6-OHDA lesions of the rat prefrontal cortex increases locomotor activity, impairs acquisition of delayed alternation tasks, but does not affect uninterupted tasks in the radial maze, Behav Res. 1990;37:157-168.
27. Sawaguchi T, Goldman-Rakic PS. Di dopamine receptors in prefrontal cortex: involvement in working memory. Science, 1991;251:947-950.
28. 2, antagonist into the prefrontal cortex. Soc Neurosci Abstr. 1995;21:1942.
29. Murphy BL, Roth RH, Arnsten AFT. The effects of FG 7142 on prefrontal cortical dopamine and spatial working memory in rat and monkey. Soc Neurosci Abstr. 1994;20:1018.
30. Murphy BL, Arnsten AFT, Goldman-Rakic PS, Roth RH, Increased dopamine turnover in the prefrontal cortex impairs spatial working memory performance in rats and monkeys, Proc Natl Acad Sci U S A. 1996;93:1325-1329.
31. Williams GV, Goldman-Rakic PS. Blockade of dopamine D, receptors enhances memory fields of prefrontal neurons in primate cerebral cortex, Nature. 1995;376:572-575.
32. Verma A, Moghaddam B, NMDA receptor antagonists impair prefrontal cortex function as assessed via spatial delayed alternation performance in rats: modulation by dopamine. J Neurosci. 1996;16:373-379.
33. Zahrt J, Taylor JR, Mathew R, Arnsten AFT. Supranormal stimulation of Dopamine receptors in the rodent prefrontal cortex impairs spatial working memory performance. J Neurosci. 1997;17:8528-8535.
34. Goldman PS. Rosvold HE. Localization of function within the dorsolateral prefrontal cortex of the rhesus monkey. Exp Neurol. 1970;27:291-304.
35. Passingham RE. Visual discrimination learning after selective prefrontal ablations in monkeys (Macaca mulatia). Neuropsychologia. 1972;10:27-39.
36. Cowey A, Gross CG. Effects of foveate prestriate and inferotemporal lesions on visual discrimination by rhesus monkeys. Exp Brain Res. 1970;11:128-144.
37. Horel JA. Misantone LJ, Visual discrimination impaired by cutting temporal lobe connections. Science. 1976;193:336-338.
38. Hanson JD, Larson ME. Snowden CT. The effects of control over high intensity noise on plasma Cortisol levels in rhesus monkeys. Behav Blol 1976;16:333-340.
39. Arguelles AE, Ibeas D, Ottone JP, Chekherdemian M, Pituitary-adrenal stimulation by sound of different frequencies, J Clin Endocrin Metab. 1962;22:846-852.
40. Arnsten AFT, Goldman-Rakic PS. Alpha-2 adrenergic mechanisms in prefrontal cortex associated with cognitive decline in aged nonhuman primates, Science. 1985;30:1273-1276.
41. Arnsten AFT. Segal DS, Janowsky OS, Judd LL, Hillyard SA. Neville H, Bloom FE. Naloxone augments electrophysiological signs of selective attention in man. Nature. 1983;304:725-727.
42. Goldstein LE. Rasmusson AM, Bunney SB, Roth RH. Role of the amygdala in the coordination of behavioral, neuroendocrine and prefrontal cortical monoamine responses to psychological stress in the rat. J Neurosci. 1996;16:4787-4798.
43. Steere JC, Li B-M, Jentsch JD, Mathews R, Taylor JR, Arnsten AFT, Alpha-1 noradrenergic stimulation impairs, while alpha-2 stimulation Improves, prefrontal cortex spatial working memory function. Soc Neurosci Abstr. 1996;22:1126.
44. Mattes JA. The role of frontal lobe dysfunction in childhood hyperkinesis. Comp Psychiatry. 1980;21:358-369.
45. Levin S. Frontal lobe dysfunction In schizophrenia, II: impairments of psychological and brain functions. J Psychiatr Res. 1984;18:27-55.
46. Weinberger DR, Berman KF. Zee RF, Physiologic dysfunction of dorsolateral prefrontal cortex in schizophrenia, I: regional cerebral blood flow evidence. Arch Gen Psychiatry. 1986;43:114-124.
47. Baxter LR, Schwartz JM, Phelps ME, Mazziota JC, Guze BH, Selin CE. Gerner RH, Sumida RM, Reduction of prefrontal cortex glucose metabolism common to three types of depression. Arch Gen Psychiatry. 1989;46:243-250.
48. Barkley RA, Grodzinsky G, DuPaul GJ, Frontal lobe functions in attention deficit disorder with and without hyperactivity: a review and research report. J Abnorm Child Psych. 1992;20:163-188.
49. Birnbaum SG, Arnsten AFT. The alpha-2A noradrenergic agonist, guanfacine, reverses the working memory deficits induced by pharmacological stress (FG 7142). Soc Neurosci Abstr. 1996;22:1126.
50. Murphy B, Roth R, Arnsten AFT, Clozapine reverses the spatial working memory deficits induced by FG 7142 in monkeys. Neuropsychopharmacology. 1997;16:433-437.
51. Lee MA, Thompson PA, Meltzer HY, Effects of clozapine on cognitive function In schizophrenia, Clin Psychiatry. 1994;55:82-87.
52. Daniel DG, Weinberger DR, Jones DW, Zigun JR, Cippola R, Handel S, Bigelow LB, Goldberg TE, Berman KF, Kleinman JE. The effect of amphetamine on regional cerebral blood flow during cognitive activation in schizophrenia. J Neurosci. 1991;11:1907-1917.
53. Davis KL, Kahn RS, Ko G, Davidson M, Dopamine in schizophrenia: a review and reonceptualization. Am J Psychiatry. 1991;148:1474-1486.
54. Grace AA. Cortical regulation of subcortical dopamine systems and its possible relevance to schizophrenia, J Neural Transm. 1993;91:111-134.
55. Bilder RM, Lieberman JA, Kim Y, Alvir JM, Reiter G, Methylphenidate and neuroleptic effects on oral word production in schizophrenia. Neuropsychiatr Neuropsychol Behav Neurol, 1992;5:262-271.