Hippocampal-dependent learning and experience-dependent activation of the hippocampus are preferentially disrupted by ethanol

Neuroscience

Volumn 74, Issue 2, 1996, Pages 313-322

  Melia, K R ^a   Ryabinin, A E ^b   Corodimas, K P ^a   Wilson, M C ^b   LeDoux, J E ^a  

^a NEW YORK UNIVERSITY   (United States)

^b SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

alcohol; c fos; context; fear conditioning; memory

Indexed keywords

ALCOHOL; MESSENGER RNA; PROTEIN C FOS;

ALCOHOL INTOXICATION; ANIMAL EXPERIMENT; ARTICLE; CONDITIONING; CONTROLLED STUDY; EXPERIENCE; FEAR; GENE EXPRESSION; HIPPOCAMPUS; MALE; MEMORY; MOTIVATION; NEOCORTEX; NONHUMAN; ONCOGENE C FOS; PRIORITY JOURNAL; RAT; STATE DEPENDENT LEARNING;

EID: 0030593451     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/0306-4522(96)00138-8     Document Type: Article

References (71)

1. Bammer G., Chesher G.B. An analysis of some effects of ethanol on performance in a passive avoidance task. Psychopharmacology. 77:1982;66-73.
2. Birnbaum M., Parker E.S., Hartley J.T., Noble E.P. Alcohol and memory: retrieval processes. J. Verb. Learn. Verb. Behav. 17:1978;325-335.
3. Blanchard R.J., Blanchard D.C. Crouching as an index of fear. J. comp. Physiol. Psychol. 67:1969;370-375.
4. Blitzer R.D., Gil O., Landau E.M. Long-term potentiation in rat hippocampus is inhibited by low concentrations of ethanol. Brain Res. 537:1990;203-208.
5. Bloom F., Lad P., Pittman Q., Rogers J. Blood alcohol levels in rats: non-uniform yields from intraperitoneal doses based on body weights. Br. J. Pharmac. 75:1982;251-254.
6. Bolles R.C., Collier A.C. The effect of predictive cues on freezing in rats. Anim. Learn. Behav. 4:1976;6-8.
7. Bolles R.C., Fanselow M.S. A perceptual defensive recuperative model of fear and pain. Behav. Brain. Sci. 3:1980;291-323.
8. Bouton M.E., Bolles R.C. Conditioned fear assessed by freezing and by the suppression of three different baselines. Anim. Learn. Behav. 8:1980;429-434.
9. Brick J., Sun J.Y., Davis L., Pohorecky L.A. Ethanol and the response to electric shock in rats. Life Sci. 18:1976;1293-1298.
10. Bullit E. Expression of c-fos like protein as a marker for neuronal activity following noxious stimulation in the rat. J. comp. Neurol. 296:1990;517-530.
11. Campeau S., Miserendino M.J.D., Davis M. Intra-amygdala infusion of the N-methyl-D-aspartate receptor antagonist AP5 blocks acquisition but not expression of fear-potentiated startle to an auditory conditioned stimulus. Behav. Neurosci. 106:1992;569-574.
12. Carlen P.L., Gurevich N., Durand D. Ethanol in low doses augments calcium-mediated mechanisms measured intracellularly in hippocampal neurons. Science. 215:1982;306-309.
13. Chomczynski P., Sacchi N. Single step method of RNA isolation by acid gaunidinium thiocyanate-phenol-chloroform extraction. Analyt. Biochem. 162:1987;156-169.
14. Cohen N. J. (1984) Preserved learning capacity in amnesia: evidence for multiple memory systems. In The Neuropsychology of Memory (eds Butters N. and Squire L. R.), pp. 83-103. Guilford Press, New York.
15. Criado J.R., Steffenson S.C., Henriksen S.J. Ethanol acts via ventral tegmental area to influence hippocampal physiology. Synapse. 17:1994;84.
16. Devenport L.D., Merriman V.J., Devenport J.A. Effects of ethanol on enforced spatial variability in the 8-arm radial maze. Pharmac. Biochem. Behav. 18:1983;55-59.
17. Dragunow M., Faull R. The use of c-fos as a metabolic marker in neuronal pathway tracing. J. Neurosci. Meth. 29:1989;261-265.
18. Durand D., Corrigall W.A., Kujtan P., Carlen P.L. Effects of low concentrations of ethanol on CA1 hippocampal neurons in vitro. Can. J. Physiol. Pharmac. 59:1981;979-984.
19. Eichenbaum H., Otto T., Cohen N.J. The hippocampus: what does it do? Behav. Neural Biol. 57:1992;2-36.
20. Fanselow M.S. Conditional and unconditional components of post-shock freezing. Pav. J. Biol. Sci. 15:1980;177-182.
21. Fanselow M.S. Factors governing one-trial contextual conditioning. Anim. Learn. Behav. 18:1990;264-270.
22. Girden E., Culler E. Conditioned responses in curarized striated muscle in dogs. J. comp. Psychol. 23:1937;261-274.
23. Givens B.S., Breese G.R. Site-specific enhancement of γ-aminobutyric acid-mediated inhibition of neural activity by ethanol in the rat medial septal area. J. Pharmac. exp. Ther. 254:1990;528-538.
24. Gizang-Ginsberg E., Ziff E.B. Nerve growth factor regulates tyrosine hydroxylase gene transcription through a nucleoprotein complex that contains c-fos. Genes Dev. 4:1990;477-491.
25. Glowa J.R., Crawley J., Suzdak P.D., Paul S.M. Ethanol and the GABA receptor complex: studies with the partial inverse benzodiazepine receptor agonist R015-4513. Pharmac. Biochem. Behav. 31:1989;767-772.
26. Goodwin D.W., Powell B., Bremer D., Hoine H., Stern J. Alcohol and recall: state dependent effects in man. Science. 163:1969;1358-1360.
27. Greenberg D.A., Cooper E.C., Gordon A., Diamond I. Ethanol and the γ-aminobutyric acid-benzodiazepine receptor complex. J. Neurochem. 42:1984;1062-1068.
28. Harris R.A., Brodie M.S., Dunwiddie T.Y. Possible substrates of ethanol reinforcement: GABA and dopamine. Ann. N.Y. Acad. Sci. 654:1992;61-69.
29. Hengerer B., Lindholm D., Heumann R., Ruther U., Wagner E.F., Thoenen H. Lesion induced increases in nerve growth factor mRNA is mediated by c-fos. Proc. natn. Acad. Sci. U.S.A. 87:1990;3899-3903.
30. Holloway F.A. State-dependent effects of ethanol on active avoidance and passive avoidance learning. Psychopharmacology. 25:1972;238-261.
31. Jarrard L.E. On the role of the hippocampus in learning and memory in the rat. Behav. Neural Biol. 60:1993;9-26.
32. Jones B.M. Memory impairment on the ascending and descending limbs of the blood alcohol curve. J. abnorm. Psychol. 82:1973;24-32.
33. Kim J.J., Fanselow M.S. Modality-specific retrograde amnesia of fear. Science. 256:1992;675-677.
34. Koob G.F., Bloom F.E. Cellular and molecular mechanisms of drug dependence. Science. 242:1988;715-723.
35. LeDoux J. Emotion: clues from the brain. A. Rev. Neurosci. 46:1995;209-235.
36. LeDoux J.E., Sakaguchi A., Reis D.J. Subcortical efferent projections of the medial geniculate nucleus mediate emotional responses conditioned to acoustic stimuli. J. Neurosci. 4:1984;683-698.
37. Lister R. G., Eckardt M. J. and Weingartner H. (1987) Ethanol intoxication and memory. In Recent Developments in Alcoholism (ed. Galanter M.), pp. 111-126. Plenum Press, New York.
38. Lister R.G., Gorenstein C., Risher-Flowers D., Weingartner H.J., Eckardt M.J. Dissociation of the acute effects of alcohol on implicit and explicit memory processes. Neuropsychology. 29:1991;1205-1212.
39. Lovinger D.M., White G., Weight F.F. Ethanol inhibits NMDA-activated ion current in hippocampal neurons. Science. 243:1989;1721-1724.
40. Lovinger D.M., White G., Weight F.F. NMDA receptor-mediated synaptic excitation selectively inhibited by ethanol in hippocampal slice from adult rat. J. Neurosci. 10:1990;1372-1379.
41. MacInnes J.W., Uphouse L.L. Effects of alcohol on acquisition and retention of passive-avoidance conditioning in different mouse strains. J. comp. Physiol. Psychol. 84:1973;398-402.
42. Mancillas J.R., Siggins G.R., Bloom F.E. Systemic ethanol: enhancement of responses to acetylcholine and somatostatin in hippocampus. Science. 231:1986;161-163.
43. Mathews D., Simson P.E., Best P.J. Ethanol disrupts activity of hippocampal place cells in awake behaving rats (Abstract). Alcohol. clin. exp. Res. 18:1994;520.
44. McNaughton B. L. and Barnes C. A. (1990) From cooperative synaptic enhancement to associative memory: bridging the abyss. In Seminars in the Neurosciences (eds Gustafsson B. and Wigstrom H.), pp. 403-466. Saunders London.
45. Melchior C.L., Glasky A.J., Ritzmann R.F. A low dose of ethanol impairs working memory in mice in a win-shift foraging paradigm. Alcohol. 10:1993;491-493.
46. Melia K.F., Ehlers C.L. Signal detection analysis of ethanol effects on a complex conditional discrimination. Pharmac. Biochem. Behav. 33:1989;581-584.
47. Melia K.F., Koob G., Ehlers C.L. Ethanol effects on delayed spatial matching as modeled by a negative exponential forgetting function. Psychopharmacology. 102:1990;391-398.
48. Melia K.R., Ryabinin A.E., Schroeder R., Bloom F.E., Wilson M.C. Induction and habituation of immediate early gene expression in rat brain by acute and repeated restraint stress. J. Neurosci. 14:1994;5929-5938.
49. Moghaddam B., Boliano M.L. Biphasic effect of ethanol on extracellular accumulation of glutamate in the hippocampus and the nucleus acumbens. Neurosci. Lett. 178:1995;99-102.
50. Morgan J.I., Cohen D.R., Hempstead J.L., Curran T. Mapping patterns of c-fos expression in the central nervous system after seizure. Science. 237:1987;192-197.
51. Morgan J.I., Curran T. Stimulus-transcription coupling in the nervous system: involvement of the inducible proto-oncogenes fos and jun. A. Rev. Neurosci. 14:1991;421-451.
52. Nabeshima T., Tohyama K., Kameyama T. Reversal of alcohol-induced amnesia by the benzodiazepine inverse agonist RO-154513. Eur. J. Pharmac. 155:1988;211-217.
53. Naranjo J.R., Mellstrom B., Achaval M., Sassone-Corsi P. Molecular pathways of pain: Fos/Jun activation of a noncanonical AP-1 site in the prodynorphin gene. Neuron. 6:1991;607-617.
54. Neuenschwander-El Massioui N., Dutrieux G., Edeline J.M. Conditioned hippocampal cellular response to a behaviorally silent conditioned stimulus. Behav. Neurosci. 105:1991;313-325.
55. O'Keefe J. and Nadel L. (1978) The Hippocampus as a Cognitive Map. Clarendon Press, Oxford.
56. Parkin A. J. (1987) Memory and Amnesia. Blackwell, Oxford.
57. Phillips R.G., LeDoux J.E. Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning. Behav. Neurosci. 106:1992;274-285.
58. Phillips R.G., LeDoux J.E. Lesions of the dorsal hippocampal formation interfere with background but not foreground contextual fear conditioning. Learn. Memory. 1:1994;34-44.
59. Pohorecky L.A. Interaction of ethanol and stress: research with experimental animals - an update. Alcohol Alcohol. 25:1990;263-276.
60. Rudy J.W. Contextual conditioning and auditory cue conditioning dissociate during development. Behav. Neurosci. 107:1993;887-891.
61. Ryabinin A.E., Melia K.R., Cole M., Bloom F.E., Wilson M.C. Alcohol selectively attenuates stress-induced c-fos expression in rat hippocampus. J. Neurosci. 15:1995;721-730.
62. Schreiber S.S., Tocco G., Shors T.J., Thompson R.F. Activation of immediate early genes after acute stress. NeuroReport. 2:1991;17-20.
63. Selden N.R.W., Everitt B.J., Jarrard L.E., Robbins T.W. Complimentary roles for the amygdala and hippocampus in aversive conditioning to explicit and contextual cues. Neuroscience. 42:1991;335-350.
64. Siggins G.R., Pittman Q.J., French E.D. Effects of ethanol on CA1 and CA3 pyramidal cells in the hippocampal slice preparation: an intracellular study. Brain Res. 414:1987;22-34.
65. Smith M.A., Banerjee S., Gold P.W., Glowa J. Induction of c-fos mRNA in rat brain by conditioned and unconditioned stressors. Brain Res. 578:1992;135-141.
66. Sparks P.D., LeDoux J.E. Septal lesions potentiate freezing behavior to contextual but not to phasic conditioned stimuli in rats. Behav. Neurosci. 109:1995;184-188.
67. Squire L. (1987) Memory and Brain. Oxford University Press, New York.
68. Squire L.R., Knowlton B., Musen G. The structure and organization of memory. A. Rev. Psychol. 44:1993;453-495.
69. Steffensen S.C., Yeckel M.F., Miller D.R., Henriksen S.J. Ethanol-induced suppression of hippocampal long-term potentiation is blocked by lesions of the septohippocampal nucleus. Alcohol. clin. exp. Res. 17:1993;655-659.
70. Sutherland R.J., Rudy J.W. Configural association theory: the role of the hippocampal formation in learning, memory and amnesia. Psychobiology. 17:1989;129-144.
71. Young S.L., Bohenek D.L., Fanselow M.S. NMDA processes mediate anterograde amnesia of contextual fear conditioning induced by hippocampal damage: immunization against amnesia by context preexposure. Behav. Neurosci. 108:1994;19-29.