Abstract
Alcoholic dementia is a disorder characterized by multiple cognitive deficits that include memory impairment associated with one or more cognitive disturbances listed in the present text. First, we characterize the disorder and describe aspects of using nonhuman models for studying specific and particular patterns of behavioral failures and biological dysfunctions found in cases of chronic alcohol consumption. Some kinds of animal models are depicted. Although there is no experimental model that displays all aspects considered as criteria for the diagnosis of alcoholic dementia, an animal model that is considered to be the most satisfactory to study behavioral and neurobiological aspects of this disease is that in which both high/chronic ethanol exposure and thiamine deficiency variables could be controlled. In this chapter, we show that animal models that manipulate only a single recognized etiological factor are less effective to elucidate the multiple influences that lead to alcoholic dementia. We conclude that even considering that only particular aspects of this disease could be approached using experimental animals; these studies can shed light on the biological processes, causing specific and particular patterns of cognitive failure.
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References
Ruitenberg A, Van Swieten JC, Witteman JC, Mehta KM, van Duijn CM, Hofman A, Breteler MM (2002) Alcohol consumption and risk of dementia: the Rotterdam Study. Lancet 359(9303):281–286
Pfefferbaum A (2004) Alcoholism damages the brain, but does moderate alcohol use? Lancet Neurol 3(3):143–144
Robles N, Sabria J (2008) Effects of moderate chronic ethanol consumption on hippocampal nicotinic receptors and associative learning. Neurobiol Learn Mem 89(4):497–503
Balodis IM, Johnsrude IS, Olmstead MC (2007) Intact preference conditioning in acute intoxication despite deficient declarative knowledge and working memory. Alcohol Clin Exp Res 31(11):1800–1810
Weiss E, Marksteiner J (2007) Alcohol-related cognitive disorders with a focus on neuropsychology. Int J Disab Hum Dev 6(4):337–342
Hernandez OH, Vogel-Sprott M, Ke-Aznar VI (2007) Alcohol impairs the cognitive component of reaction time to an omitted stimulus: A replication and an extension. J Stud Alcohol Drugs 68(2):276–281
Bartholow BD, Pearson M, Sher KJ, Wieman LC, Fabiani M, Gratton G (2003) Effects of alcohol consumption and alcohol susceptibility on cognition: a psychophysiological examination. Biol Psychol 64(1–2):167–190
Wegner AJ, Fahle M (1999) Alcohol and visual performance. Prog Neuro-Psychopharm Biol Psychiatry 23(3):465–482
Finnigan F, Schulze D, Smalwood J (2007) Alcohol and the wandering mind: A new direction in the study of alcohol on attentional lapses. Int J Disabil Hum Dev 6(2):189–199
Hildebrandt H, Brokate B, Eling P, Lanz M (2004) Response shifting and inhibition, but not working memory, are impaired after long-term heavy alcohol consumption. Neuropsychology18(2):203–211
Flannery B, Fishbein D, Krupitsky E, Langevin D, Verbitskaya E, Bland C, Bolla K, Egorova V, Bushara N, Tsoy M, Zvartau E (2007) Gender differences in neurocognitive functioning among alcohol-dependent Russian patients. Alcohol Clin Exp Res 31(5):745–754
American Psychiatric Association (1994) Diagnostic criteria from DSM–IV. American Psychiatric Association, Washington, DC
Moriyama Y, Mimura M, Kato M, Kashima H (2006) Primary alcoholic dementia and alcohol-related dementia. Psychogeriatrics 6(3):114–118
Homewood J, Bond NW (1999) Thiamine deficiency and Korsakoff’s syndrome: failure to find memory impairments following nonalcoholic Wernicke’s encephalopathy. Alcohol 19(1):75–84
Butterworth RF (1995) Pathophysiology of alcoholic brain damage – Synergistic effects of alcohol, thiamine-deficiency and alcoholic liver-disease. J Neurochem 65:S202
Harper C (1979) Wernicke’s encephalopathy: a more common disease than realised. A neuropathological study of 51 cases. J Neurol Neurosurg Psychiatry 42(3):226–231
Pfefferbaum A, Sullivan EV, Hedehus M, Adalsteinsson E, Lim KO, Moseley M (2000) In vivo detection and functional correlates of white matter microstructural disruption in chronic alcoholism. Alcohol Clin Exp Res 24(8):1214–1221
Harper C (1998) The neuropathology of alcohol-specific brain damage, or does alcohol damage the brain? J Neuropathol Exp Neurol 57(2):101–110
Oslin D, Atkinson RM, Smith DM, Hendrie H (1998) Alcohol related dementia: proposed clinical criteria. Int J Geriatr Psychol 13(4):203–212
Oslin DW, Cary MS (2003) Alcohol-related dementia: validation of diagnostic criteria. Am J Geriatr Psychiatry 11(4):441–447
Hoyumpa AM Jr (1980) Mechanisms of thiamine deficiency in chronic alcoholism. Am J Clin Nutr 33(12):2750–2761
Laforenza U, Patrini C, Gastaldi G, Rindi G (1990) Effects of acute and chronic ethanol administration on thiamine metabolizing enzymes in some brain areas and in other organs of the rat. Alcohol Alcohol 25(6):591–603
Pincus JH, Wells K (1972) Regional distribution of thiamine-dependent enzymes in normal and thiamine-deficient brain. Exp Neurol 37(3):495–501
Langlais PJ (1995) Alcohol-related thiamine deficiency impact on cognitive and memory functioning. Alcohol Health Res World 19(2):113–121
Harper C (1983) The incidence of Wernicke’s encephalopathy in Australia – a neuropathological study of 131 cases. J Neurol Neurosurg Psychiatry 46(7):593–598
Victor M (1994) Alcoholic dementia. Can J Neurol Sci 21(2):88–99
Thomson AD, Cook CC, Guerrini I, Sheedy D, Harper C, Marshall EJ (2008) Wernicke’s encephalopathy: ‘Plus ca change, plus c’est la meme chose’. Alcohol Alcohol 43(2):180–186
Sechi G, Serra A (2007) Wernicke’s encephalopathy: new clinical settings and recent advances in diagnosis and management. Lancet Neurol 6(5):442–455
Chick J (1997) Alcohol and the brain. Curr Opin Psychiatry 10(3):205–210
Kopelman MD (1985) Rates of forgetting in Alzheimer-type dementia and Korsakoffs syndrome. Neuropsychologia 23(5):623–638
Victor M, Adams RD, Collins GH (1989) The Wernicke-Korsakoff syndrome and related neurological disorders due to alcoholism and malnutrition, 2nd edn. F.A.Davis, Philadelphia, PA
Martin PR, Singleton CK, Hiller-Sturmhofel S (2003) The role of thiamine deficiency in alcoholic brain disease. Alcohol Res Health 27(2):134–142
Naidoo DP, Bramdev A, Cooper K (1996) Autopsy prevalence of Wernicke’s encephalopathy in alcohol-related disease. S Afr Med J 86(9):1110–1112
He X, Sullivan EV, Stankovic RK, Harper CG, Pfefferbaum A (2007) Interaction of thiamine deficiency and voluntary alcohol consumption disrupts rat corpus callosum ultrastructure. Neuropsychopharmacology 32(10):2207–2216
McIntosh C, Chick J (2004) Alcohol and the nervous system. J Neurol Neurosurg Psychiatry 75:16–21
Tabakoff B, Hoffman PL (2000) Animal models in alcohol research. Alcohol Res Health 24(2):77–84
Cohen NJ, Squire LR (1981) Retrograde-amnesia and remote memory impairment. Neuropsychologia 19(3):337–356
Becker JT, Butters N, Rivoira P, Miliotis P (1986) Asking the right questions: Problem solving in male alcoholics and male alcoholics with Korsakoff’s syndrome. Alcohol Clin Exp Res 10(6):641–646
Milner B, Corkin S, Teuber HL (1968) Further analysis of the hippocampal amnesic syndrome: 14-year follow-up study of H.M. Neuropsychologia 6(3):215–234
Pollonini G, Gao V, Rabe A, Palminiello S, Albertini G, Alberini CM (2008) Abnormal expression of synaptic proteins and neurotrophin-3 in the down syndrome mouse model Ts65Dn. Neuroscience 156(1):99–106
Savvaki M, Panagiotaropoulos T, Stamatakis A, Sargiannidou I, Karatzioula P, Watanabe K, Stylianopoulou F, Karagogeos D, Kleopa KA (2008) Impairment of learning and memory in TAG-1 deficient mice associated with shorter CNS internodes and disrupted juxtaparanodes. Mol Cell Neurosci 39(3):478–490
Wang Q, Liu Y, Zou X, Wang Q, An M, Guan X, He J, Tong Y, Ji J (2008) The hippocampal proteomic analysis of senescence-accelerated mouse: implications of Uchl3 and mitofilin in cognitive disorder and mitochondria dysfunction in SAMP8. Neurochem Res 33(9):1776–1782
Kesner RP, Novak JM (1982) Serial position curve in rats: role of the dorsal hippocampus. Science 218(4568):173–175
Squire LR, Spanis CW (1984) Long gradient of retrograde amnesia in mice: continuity with the findings in humans. Behav Neurosci 98(2):345–348
Getachew B, Hauser SR, Taylor RE, Tizabi Y (2008) Desipramine blocks alcohol-induced anxiety- and depressive-like behaviors in two rat strains. Pharmacol Biochem Behav 91(1):97–103
Oliveira-Silva IF, Pinto L, Pereira SR, Ferraz VP, Barbosa AJ, Coelho VA, Gualberto FF, Souza VF, Faleiro RR, Franco GC, Ribeiro AM (2007) Age-related deficit in behavioural extinction is counteracted by long-term ethanol consumption: correlation between 5-HIAA/5HT ratio in dorsal raphe nucleus and cognitive parameters. Behav Brain Res 180(2):226–234
Arendt T, Allen Y, Marchbanks RM, Schugens MM, Sinden J, Lantos PL, Gray JA (1989) Cholinergic system and memory in the rat – effects of chronic ethanol, embryonic basal forebrain brain transplants and excitotoxic lesions of cholinergic basal forebrain projection system. Neuroscience 33(3): 435–462
Spanagel R (2003) Alcohol addiction research: from animal models to clinics. Best Pract Res Clin Gastroenterol 17(4):507–518
Heilig M, Egli M (2008) Models for alcohol dependence: a clinical perspective. Drug Discov Today: Dis Models 2(4):313–318
Koob GE, Le Moal M (2008) Addiction and the brain antireward system. Annu Rev Psychol 59:29–53
Spanagel R, Holter SM (2000) Pharmacological validation of a new animal model of alcoholism. J Neural Transm 107(6):669–680
Walker BM, Koob GF (2008) Pharmacological evidence for a motivational role of kappa-opioid systems in ethanol dependence. Neuropsychopharmacology 33(3):643–652
Dhaher R, Finn D, Snelling C, Hitzemann R (2008) Lesions of the extended amygdala in C57BL/6J mice do not block the intermittent ethanol vapor-induced increase in ethanol consumption. Alcohol Clin Exp Res 32(2):197–208
Zhao Y, Weiss F, Zorrilla EP (2007) Remission and resurgence of anxiety-like behavior across protracted withdrawal stages in ethanol-dependent rats. Alcohol Clin Exp Res 31(9):1505–1515
O’Dell LE, Roberts AJ, Smith RT, Koob GF (2004) Enhanced alcohol self-administration after intermittent versus continuous alcohol vapor exposure. Alcohol Clin Exp Res 28(11):1676–1682
Funk CK, Zorrilla EP, Lee MJ, Rice KC, Koob GF (2007) Corticotropin-releasing factor 1 antagonists selectively reduce ethanol self-administration in ethanol-dependent rats. Biol Psychiatry 61(1):78–86
Tomlinson D, Wilce P, Bedi KS (1998) Spatial learning ability of rats following differing levels of exposure to alcohol during early postnatal life. Physiol Behav 63(2):205–211
Ehlers CL, Somes C, Li TK, Lumeng L, Hwang BH, Jimenez P, Mathe AA (1999) Calcitonin gene-related peptide (CGRP) levels and alcohol. Int J Neuropsychopharmacol 2(3):173–179
Hodges H, Allen Y, Sinden J, Mitchell SN, Arendt T, Lantos PL, Gray JA (1991) The effects of cholinergic drugs and cholinergic-rich foetal neural transplants on alcohol-induced deficits in radial maze performance in rats. Behav Brain Res 41(1):7–28
Cadete-Leite A, Brandao F, Andrade JP, Ribeiro-da-Silva A, Paula-Barbosa MM (1997) The GABAergic system of the dentate gyrus after withdrawal from chronic alcohol consumption: effects of intracerebral grafting and putative neuroprotective agents. Alcohol Alcohol 32(4):471–484
Carroll MR, Rodd ZA, Murphy JM, Simon JR (2006) Chronic ethanol consumption increases dopamine uptake in the nucleus accumbens of high alcohol drinking rats. Alcohol 40(2):103–109
Christie BR, Swann SE, Fox CJ, Froc D, Lieblich SE, Redila V, Webber A (2005) Voluntary exercise rescues deficits in spatial memory and long-term potentiation in prenatal ethanol-exposed male rats. Eur J Neurosci 21(6):1719–1726
Baird TJ, Vanecek SA, Briscoe RJ, Vallett M, Carl KL, Gauvin DV (1998) Moderate, long-term, alcohol consumption potentiates normal, age-related spatial memory deficits in rats. Alcohol Clin Exp Res 22(3):628–636
Byrnes ML, Richardson DP, Brien JF, Reynolds JN, Dringenberg HC (2004) Spatial acquisition in the Morris water maze and hippocampal long-term potentiation in the adult guinea pig following brain growth spurt-prenatal ethanol exposure. Neurotoxicol Taratol 26(4):543–551
Pires RGW, Pereira SRC, Pittella JEH, Franco GC, Ferreira CLM, Fernandes PA, Ribeiro AM (2001) The contribution of mild thiamine deficiency and ethanol consumption to central cholinergic parameter dysfunction and rats’ open-field performance impairment. Pharmacol Biochem Behav 70(2–3):227–235
Eriksson K (1968) Genetic selection for voluntary alcohol consumption in the albino rat. Science 159(3816):739–741
Sinclair JD, Le AD, Kiianmaa K (1989) The AA and ANA rat lines, selected for differences in voluntary alcohol consumption. Experientia 45(9):798–805
Colombo G, Agabio R, Diaz G, Fa M, Lobina C, Reali R, Gessa GL (1997) Sardinian alcohol-preferring rats prefer chocolate and sucrose over ethanol. Alcohol 14(6):611–615
Li TK, Lumeng L, Doolittle DP (1993) Selective breeding for alcohol preference and associated responses. Behav Genet 23(2):163–170
Ghozland S, Chu K, Kieffer BL, Roberts AJ (2005) Lack of stimulant and anxiolytic-like effects of ethanol and accelerated development of ethanol dependence in mu-opioid receptor knockout mice. Neuropharmacology 49(4):493–501
Thiele TE, Naveilhan P, Ernfors P (2004) Assessment of ethanol consumption and water drinking by NPY Y(2) receptor knockout mice. Peptides 25(6):975–983
Han DH, Lyool IK, Sung YH, Lee SH, Renshaw PE (2008) The effect of acamprosate on alcohol and food craving in patients with alcohol dependence. Drug Alcohol Depend 93(3):279–283
Snyder JL, Bowers TG (2008) The efficacy of acamprosate and naltrexone in the treatment of alcohol dependence: a relative benefits analysis of randomized controlled trials. Am J Drug Alcohol Abuse 34(4):449–461
Zalewska-Kaszubska J, Gorska D, Dyr W, Czarnecka E (2008) Effect of chronic acamprosate treatment on voluntary alcohol intake and beta-endorphin plasma levels in rats selectively bred for high alcohol preference. Neurosci Lett 431(3):221–225
Savage LM, Chang Q, Gold PE (2003) Diencephalic damage decreases hippocampal acetylcholine release during spontaneous alternation testing. Learn Mem 10(4):242–246
Langlais PJ, Savage LM (1995) Thiamine deficiency in rats produces cognitive and memory deficits on spatial tasks that correlate with tissue loss in diencephalon, cortex and white matter. Behav Brain Res 68(1):75–89
Haas RH (1988) Thiamine and the brain. Annu Rev Nutr 8:483–515
Ciccia RM, Langlais PJ (2000) An examination of the synergistic interaction of ethanol and thiamine deficiency in the development of neurological signs and long-term cognitive and memory impairments. Alcohol Clin Exp Res 24(5):622–634
Pfefferbaum A, Adalsteinsson E, Bell RL, Sullivan EV (2007) Development and resolution of brain lesions caused by pyrithiamine- and dietary-induced thiamine deficiency and alcohol exposure in the alcohol-preferring rat: a longitudinal magnetic resonance imaging and spectroscopy study. Neuropsychopharmacology 32(5):1159–1177
Dixon G, Harper CG (2001) Quantitative analysis of glutamic acid decarboxylase-immunoreactive neurons in the anterior thalamus of the human brain. Brain Res 923(1–2):39–44
Harper C (1979) Wernicke’s encephalopathy: a more common disease than realised. A neuropathological study of 51 cases. J Neurol Neurosurg Psychiatry 42(3):226–231
Pires RGW, Pereira SRC, Oliveira-Silva IF, Franco GC, Ribeiro AM (2005) Cholinergic parameters and the retrieval of learned and re-learned spatial information: a study using a model of Wernicke-Korsakoff Syndrome. Behav Brain Res 162(1):11–21
Pires RGW, Pereira SRC, Carvalho FM, Oliveira-Silva IF, Ferraz VP, Ribeiro AM (2007) Correlation between phosphorylation level of a hippocampal 86 kDa protein and extinction of a behaviour in a model of Wernicke-Korsakoff syndrome. Behav Brain Res 180(1):102–106
Ragozzino ME, Wilcox C, Raso M, Kesner RP (1999) Involvement of rodent prefrontal cortex subregions in strategy switching. Behav Neurosci 113(1):32–41
Delatour B, Gisquet-Verrier P (2000) Functional role of rat prelimbic-infralimbic cortices in spatial memory: evidence for their involvement in attention and behavioural flexibility. Behav Brain Res 109(1):113–128
Dias R, Aggleton JP (2000) Effects of selective excitotoxic prefrontal lesions on acquisition of nonmatching- and matching-to-place in the T-maze in the rat: differential involvement of the prelimbic-infralimbic and anterior cingulate cortices in providing behavioural flexibility. Eur J Neurosci 12(12):4457–4466
Carvalho FM, Pereira SRC, Pires RGW, Ferraz VP, Romano-Silva MA, Oliveira-Silva LF, Ribeiro AM (2006) Thiamine deficiency decreases glutamate uptake in the prefrontal cortex and impairs spatial memory performance in a water maze test. Pharmacol Biochem Behav 83(4):481–489
Mason ST (1983) The neurochemistry and pharmacology of extinction behavior. Neurosci Biobehav Rev 7(3):325–347
Robbins TW (1997) Arousal systems and attentional processes. Biol Psychol 45(1–3): 57–71
Parikh V, Sarter M (2008) Cholinergic mediation of attention – contributions of phasic and tonic increases in prefrontal cholinergic activity. Mol Biophys Mech Arousal Alertness Atten 1129:225–235
Bainbridge NK, Koselke LR, Jeon J, Bailey KR, Wess J, Crawley JN, Wrenn CC (2008) Learning and memory impairments in a congenic C57BL/6 strain of mice that lacks the M-2 muscarinic acetylcholine receptor subtype. Behav Brain Res 190(1):50–58
Pauli WM, O’Reilly RC (2008) Attentional control of associative learning – a possible role of the central cholinergic system. Brain Res 1202:43–53
Keverne J, Ray M (2008) Neurochemistry of Alzheimer’s disease. Psychiatry 7(1):6–8
Nardone R, Bergmann J, Tezzon F, Ladurner G, Golaszewski S (2008) Cholinergic dysfunction in subcortical ischaemic vascular dementia: a transcranial magnetic stimulation study. J Neural Transm 115(5):737–743
Arendt T, Bigl V, Arendt A, Tennstedt A (1983) Loss of neurons in the nucleus basalis of Meynert in Alzheimer’s disease, paralysis agitans and Korsakoff’s disease. Acta Neuropathol 61(2):101–108
Mair RG, Anderson CD, Langlais PJ, McEntee WJ (1988) Behavioral impairments, brain-lesions and monoaminergic activity in the rat following recovery from a bout of thiamine-deficiency. Behav Brain Res 27(3):223–239
Overstreet DH, Russell RW (1984) Selective breeding for differences in cholinergic function - sex-differences in the genetic-regulation of sensitivity to the anticholinesterase, Dfp. Behav Neural Biol 40(2):227–238
Bartus RT, Dean RL, Beer B, Lippa AS (1982) The cholinergic hypothesis of geriatric memory dysfunction. Science 217(4558):408–417
Gill SK, Ishak M, Dobransky T, Haroutunian V, Davis KL, Rylett RJ (2007) 82-kDa choline acetyltransferase is in nuclei of cholinergic neurons in human CNS and altered in aging and Alzheimer disease. Neurobiol Aging 28(7):1028–1040
Henny P, Jones BE (2008) Projections from basal forebrain to prefrontal cortex comprise cholinergic, GABAergic and glutamatergic inputs to pyramidal cells or interneurons. Eur J Neurosci 27(3):654–670
Garcia-Alloza M, Zaldua N, ez-Ariza M, Marcos B, Lasheras B, Javier Gil-Bea F, Ramirez MJ (2006) Effect of selective cholinergic denervation on the serotonergic system: implications for learning and memory. J Neuropathol Exp Neurol 65(11):1074–1081
Arendt T, Henning D, Gray JA, Marchbanks R (1988) Loss of neurons in the rat basal forebrain cholinergic projection system after prolonged intake of ethanol. Brain Res Bull 21(4):563–569
Floyd EA, Young-Seigler AC, Ford BD, Reasor JD, Moore EL, Townsel JG, Rucker HK (1997) Chronic ethanol ingestion produces cholinergic hypofunction in rat brain. Alcohol 14(1):93–98
Sugimoto H (2008) The new approach in development of anti-Alzheimer’s disease drugs via the cholinergic hypothesis. Chem Biol Interact 175(1–3):204–208
Tumiatti V, Bolognesi ML, Minarini A, Rosini M, Milelli A, Matera R, Melchiorre C (2008) Progress in acetylcholinesterase inhibitors for Alzheimer’s disease: an update. Expert Opin Ther Pat 18(4):387–401
Brousseau G, Rourke BP, Burke B (2007) Acetylcholinesterase inhibitors, neuropsychiatric symptoms, and Alzheimer’s disease subtypes: an alternate hypothesis to global cognitive enhancement. Exp Clin Psychopharmacol 15(6):546–554
Kim KY, Ke V, Adkins LM (2004) Donepezil for alcohol-related dementia: a case report. Pharmacotherapy 24(3):419–421
Cochrane M, Cochrane A, Jauhar P, Ashton E (2005) Acetylcholinesterase inhibitors for the treatment of Wernicke-Korsakoff syndrome – three further cases show response to donepezil. Alcohol Alcohol 40(2):151–154
Dong H, Csernansky CA, Martin MV, Bertchume A, Vallera D, Csernansky JG (2005) Acetylcholinesterase inhibitors ameliorate behavioral deficits in the Tg2576 mouse model of Alzheimer’s disease. Psychopharmacology (Berl) 181(1):145–152
Mohammed AH (1993) Effects of cholinesterase inhibitors on learning and memory in rats: a brief review with special reference to THA. Acta Neurol Scand Suppl 149:13–15
Melcer T, Gonzalez D, Somes C, Riley EP (1995) Neonatal alcohol exposure and early development of motor-skills in alcohol-preferring and nonpreferring rats. Neurotoxicol Taratol 17(2):103–110
Meyer LS, Kotch LE, Riley EP (1990) Alterations in gait following ethanol exposure during the brain growth spurt in rats. Alcohol-Clin Exp Res 14(1):23–27
Pascual M, Blanco AM, Cauli O, Minarro J, Guerri C (2007) Intermittent ethanol exposure induces inflammatory brain damage and causes long-term behavioural alterations in adolescent rats. Eur J Neurosci 25(2):541–550
Borlikova GG, Elbers NA, Stephens DN (2006) Repeated withdrawal from ethanol spares contextual fear conditioning and spatial learning but impairs negative patterning and induces over-responding: evidence for effect on frontal cortical but not hippocampal function? Eur J Neurosci 24(1):205–216
Santín LJ, Rubio S, Begega A, Arias JL (2000) Effects of chronic alcohol consumption on spatial reference and working memory tasks. Alcohol 20(2):149–159
Slawecki CJ (2006) Two-choice reaction time performance in Sprague-Dawley rats exposed to alcohol during adolescence or adulthood. Behav Pharmacol 17(7):605–614
Borde N, Jaffard R, Beracochea DJ (1996) Effects of methyl beta-carboline-3-carboxylate on memory impairments induced by chronic alcohol consumption in mice. Prog Neuropsychopharmacol Biol Psychiatry 20(8):1377–1387
Borde N, Beracochea DJ (1999) Effects of diazepam or chronic alcohol treatment on spatial reversal learning in mice. Pharmacol Biochem Behav 62(4):719–725
Beracochea D, Micheau J, Jaffard R (1992) Memory deficits following chronic alcohol consumption in mice: relationships with hippocampal and cortical cholinergic activities. Pharmacol Biochem Behav 42(4):749–753
Gal K, Bardos G (1994) The effect of chronic alcohol treatment on the radial maze performance of rats. Neuroreport 5(4):421–424
Casamenti F, Scali C, Vannucchi MG, Bartolini L, Pepeu G (1993) Long-term ethanol consumption by rats: effect on acetylcholine release in vivo, choline acetyltransferase activity, and behavior. Neuroscience 56(2):465–471
Garcia-Moreno LM, Conejo NM, Capilla A, Garcia-Sanchez O, Senderek K, Arias JL (2002) Chronic ethanol intake and object recognition in young and adult rats. Prog Neuropsychopharmacol Biol Psychiatry 26(5):831–837
Pereira SRC, Menezes GA, Franco GC, Costa AEB, Ribeiro AM (1998) Chronic ethanol consumption impairs spatial remote memory in rats but does not affect cortical cholinergic parameters. Pharmacol Biochem Behav 60(2):305–311
Fadda F, Cocco S, Stancampiano R, Rossetti ZL (1999) Long-term voluntary ethanol consumption affects neither spatial nor passive avoidance learning, nor hippocampal acetylcholine release in alcohol-preferring rats. Behav Brain Res 103(1):71–76
Farr SA, Scherrer JF, Banks WA, Flood JF, Morley JE (2005) Chronic ethanol consumption impairs learning and memory after cessation of ethanol. Alcohol Clin Exp Res 29(6):971–982
Irle E, Markowitsch HJ (1983) Widespread neuroanatomical damage and learning-deficits following chronic alcohol-consumption or vitamin-B1 (Thiamine) deficiency in rats. Behav Brain Res 9(3):277–294
White AM, Bae JG, Truesdale MC, Ahmad S, Wilson WA, Swartzwelder HS (2002) Chronic-intermittent ethanol exposure during adolescence prevents normal developmental changes in sensitivity to ethanol-induced motor impairments. Alcohol Clin Exp Res 26(7):960–968
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Ribeiro, A.M., Pereira, S.R.C. (2011). Animal Models of Alcohol-Induced Dementia. In: De Deyn, P., Van Dam, D. (eds) Animal Models of Dementia. Neuromethods, vol 48. Humana Press. https://doi.org/10.1007/978-1-60761-898-0_33
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