The Influence of Selection for Ethanol Withdrawal Severity on Traits Associated With Ethanol Self-Administration and Reinforcement
2010; Wiley; Volume: 35; Issue: 2 Linguagem: Inglês
10.1111/j.1530-0277.2010.01348.x
ISSN1530-0277
AutoresMatthew M. Ford, Andrea M. Fretwell, Allison M. J. Anacker, John C. Crabbe, Gregory P. Mark, Deborah A. Finn,
Tópico(s)Receptor Mechanisms and Signaling
ResumoAlcoholism: Clinical and Experimental ResearchVolume 35, Issue 2 p. 326-337 The Influence of Selection for Ethanol Withdrawal Severity on Traits Associated With Ethanol Self-Administration and Reinforcement Matthew M. Ford, Matthew M. Ford From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this authorAndrea M. Fretwell, Andrea M. Fretwell From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this authorAllison M. J. Anacker, Allison M. J. Anacker From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this authorJohn C. Crabbe, John C. Crabbe From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this authorGregory P. Mark, Gregory P. Mark From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this authorDeborah A. Finn, Deborah A. Finn From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this author Matthew M. Ford, Matthew M. Ford From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this authorAndrea M. Fretwell, Andrea M. Fretwell From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this authorAllison M. J. Anacker, Allison M. J. Anacker From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this authorJohn C. Crabbe, John C. Crabbe From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this authorGregory P. Mark, Gregory P. Mark From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this authorDeborah A. Finn, Deborah A. Finn From the Department of Behavioral Neuroscience (MMF, AMF, AMJA, JCC, GPM, DAF), Oregon Health & Science University; and Portland Alcohol Research Center (AMF, JCC, DAF), Veterans Affairs Medical Center, Portland, Oregon.Search for more papers by this author First published: 10 November 2010 https://doi.org/10.1111/j.1530-0277.2010.01348.xCitations: 12 Reprint requests: Matthew M. Ford, PhD, Department of Behavioral Neuroscience (L-470), Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239-3098; Tel.: 503-346-0050; Fax: 503-494-6877; E-mail: [email protected]. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat Abstract Background: Several meta-analyses indicate that there is an inverse genetic correlation between ethanol preference drinking and ethanol withdrawal severity, but limited work has characterized ethanol consumption in 1 genetic animal model, the Withdrawal Seizure-Prone (WSP) and-Resistant (WSR) mouse lines selected for severe or mild ethanol withdrawal, respectively. Methods: We determined whether line differences existed in: (i) operant self-administration of ethanol during sucrose fading and under different schedules of reinforcement, followed by extinction and reinstatement of responding with conditioned cues and (ii) home cage drinking of sweetened ethanol and the development of an alcohol deprivation effect (ADE). Results: Withdrawal Seizure-Prone-1 mice consumed more ethanol than WSR-1 mice under a fixed ratio (FR)-4 schedule as ethanol was faded into the sucrose solution, but this line difference dissipated as the sucrose was faded out to yield an unadulterated 10% v/v ethanol solution. In contrast, WSR-1 mice consumed more ethanol than WSP-1 mice when a schedule was imposed that procedurally separated appetitive and consummatory behaviors. After both lines achieved the extinction criterion, reinstatement was serially evaluated following oral ethanol priming, light cue presentation, and a combination of the 2 cues. The light cue produced maximal reinstatement of responding in WSP-1 mice, whereas the combined cue was required to produce maximal reinstatement of responding in WSR-1 mice. There was no line difference in the home cage consumption of a sweetened ethanol solution over a period of 1 month. Following a 2-week period of abstinence, neither line developed an ADE. Conclusions: Although some line differences in ethanol self-administration and reinstatement were identified between WSP-1 and WSR-1 mice, the absence of consistent divergence suggests that the genes underlying these behaviors do not reliably overlap with those that govern withdrawal severity. References Bäckström P, Hyytiä P (2004) Ionotropic glutamate receptor antagonists modulate cue-induced reinstatement of ethanol-seeking behavior. Alcohol Clin Exp Res 28: 558–565. Bäckström P, Hyytiä P (2005) Suppression of alcohol self-administration and cue-induced reinstatement of alcohol seeking by the mGlu2/3 receptor agonist LY379268 and the mGlu8 receptor agonist (S)-3,4-DCPG. Eur J Pharmacol 528: 110–118. Balster RL, Wiley JL, Tokarz ME, Tabakoff B (1993) Effects of ethanol and NMDA antagonists on operant behavior in ethanol Withdrawal Seizure–Prone and –Resistant mice. Behav Pharmacol 4: 107–113. Barbera TJ, Baca K, George FR (1994) Regulation of operant ethanol-reinforced behavior is genetically independent of regulation of withdrawal severity in WSP and WSR mice. Alcohol 11: 371–377. Bell RL, Rodd ZA, Boutwell CL, Hsu CC, Lumeng L, Murphy JM, Li T-K, McBride WJ (2004) Effects of long-term episodic access to ethanol on the expression of an alcohol deprivation effect in low alcohol-consuming rats. Alcohol Clin Exp Res 28: 1867–1874. Chester JA, Risinger FO, Cunningham CL (1998) Ethanol reward and aversion in mice bred for sensitivity to ethanol withdrawal. Alcohol Clin Exp Res 22: 468–473. Crabbe JC, Kosobud A, Young ER, Tam BR, McSwigan JD (1985) Bidirectional selection for susceptibility to ethanol withdrawal seizures in Mus musculus. Behav Genet 15: 521–536. Crabbe JC, Phillips TJ, Cunningham CL, Belknap JK (1992) Genetic determinants of ethanol reinforcement. Ann NY Acad Sci 654: 302–310. Crabbe JC, Phillips TJ, Kosobud A, Belknap JK (1990) Estimation of genetic correlation: interpretation of experiments using selectively bred and inbred animals. Alcohol Clin Exp Res 14: 141–151. Crawley JN, Belknap JK, Collins A, Crabbe JC, Frankel W, Henderson N, Hitzemann RJ, Maxson SC, Miner LL, Silva AJ, Wehner JM, Wynshaw-Boris A, Paylor R (1997) Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies. Psychopharmacology 132: 107–124. Czachowski CL, Santini LA, Legg BH, Samson HH (2002) Separate measures of ethanol seeking and drinking in the rat: effects of remoxipride. Alcohol 28: 39–46. Elmer GI, Meisch RA, George FR (1987) Differential concentration-response curves for oral ethanol self-administration in C57BL/6J and BALB/cJ mice. Alcohol 4: 63–68. Epstein DH, Preston KL, Stewart J, Shaham Y (2006) Toward a model of drug relapse: an assessment of the validity of the reinstatement procedure. Psychopharmacology 189: 1–16. Finn DA, Mark GP, Fretwell AM, Gililland KR, Strong MN, Ford MM (2008) Reinstatement of ethanol and sucrose seeking by the neurosteroid allopregnanolone in C57BL/6 mice. Psychopharmacology 201: 423–433. Ford MM, Fretwell AM, Mark GP, Finn DA (2007a) Influence of reinforcement schedule on ethanol consumption patterns in non-food restricted male C57BL/6J mice. Alcohol 41: 21–29. Ford MM, Fretwell AM, Nickel JD, Mark GP, Strong MN, Yoneyama N, Finn DA (2009) The influence of mecamylamine on ethanol and sucrose self-administration. Neuropharmacology 57: 250–258. Ford MM, Mark GP, Nickel JD, Phillips TJ, Finn DA (2007b) Allopregnanolone influences the consummatory processes that govern ethanol drinking in C57BL/6J mice. Behav Brain Res 179: 265–272. Hitzemann R, Edmunds S, Wu W, Malmanger B, Walter N, Belknap J, Darakjian P, McWeeney S (2009) Detection of reciprocal quantitative trait loci for acute ethanol withdrawal and ethanol consumption in heterogeneous stock mice. Psychopharmacology 203: 713–722. Khisti RT, Wolstenholme J, Shelton KL, Miles MF (2006) Characterization of the ethanol-deprivation effect in substrains of C57BL/6 mice. Alcohol 40: 119–126. Kosobud A, Bodor AS, Crabbe JC (1988) Voluntary consumption of ethanol in WSP, WSC and WSR selectively bred mouse lines. Pharmacol Biochem Behav 29: 601–607. Kosobud AE, Crabbe JC (1995) Genetic influences on the development of physical dependence and withdrawal in animals, in The Genetics of Alcoholism ( H Begleiter, B Kissin eds), pp 221–256. Oxford University Press, Oxford. Lê AD, Shaham Y (2002) Neurobiology of relapse to alcohol in rats. Pharmacol Ther 94: 137–156. Little HJ (2000) Behavioral mechanisms underlying the link between smoking and drinking. Alcohol Res Health 24: 215–224. Meisch RA (2001) Oral drug self-administration: an overview of laboratory animal studies. Alcohol 24: 117–128. Melendez RI, Middaugh LD, Kalivas PW (2006) Development of an alcohol deprivation and escalation effect in C57BL/6J mice. Alcohol Clin Exp Res 30: 2017–2025. Metten P, Crabbe JC (1996) Dependence and withdrawal, in Pharmacological Effects of Ethanol on the Nervous System ( RA Deitrich, VG Erwin eds), pp 269–290. CRC Press, New York. Metten P, Crabbe JC (2005) Alcohol withdrawal severity in inbred mouse (Mus musculus) strains. Behav Neurosci 119: 911–925. Metten P, Phillips TJ, Crabbe JC, Tarantino LM, McClearn G, Plomin R, Erwin VG, Belknap JK (1998) High genetic susceptibility to ethanol withdrawal predicts low ethanol consumption. Mamm Genome 9: 983–990. National Research Council of the National Academies (2003) Guide for the Care and Use of Mammals in Neuroscience and Behavioral Research. National Academies Press, Washington, DC. Nickel JD, Ford MM, Yoneyama N, Murillo AR, Finn DA (2006) Modulation of ethanol intake patterns in male and female Srd5a1 knockout mice. Alcohol Clin Exp Res 30: 65A. Nie H, Janak PH (2003) Comparison of reinstatement of ethanol- and sucrose-seeking by conditioned stimuli and priming injections of allopregnanolone after extinction in rats. Psychopharmacology 168: 222–228. Roberts AJ, Heyser CJ, Koob GF (1999) Operant self-administration of sweetened versus unsweetened ethanol: effects on blood alcohol levels. Alcohol Clin Exp Res 23: 1151–1157. Roberts AJ, McDonald JS, Heyser CJ, Kieffer BL, Matthes HW, Koob GF, Gold LH (2000) Mu-opioid receptor knockout mice do not self-administer alcohol. J Pharmacol Exp Ther 293: 1002–1008. Rodd-Hendricks ZA, McKinzie DL, Shaikh SR, Murphy JM, McBride WJ, Lumeng L, Li T-K (2000) Alcohol deprivation effect is prolonged in the alcohol-preferring (P) rat after repeated deprivations. Alcohol Clin Exp Res 24: 8–16. Samson HH (1986) Initiation of ethanol reinforcement using a sucrose-substitution procedure in food- and water-sated rats. Alcohol Clin Exp Res 10: 436–442. Samson HH, Chappell A (2002) Reinstatement of ethanol seeking responding after ethanol self-administration. Alcohol 26: 95–101. Samson HH, Czachowski CL, Slawecki CJ (2000) A new assessment of the ability of oral ethanol to function as a reinforcing stimulus. Alcohol Clin Exp Res 24: 766–773. Samson HH, Slawecki CJ, Sharpe AL, Chappell A (1998) Appetitive and consummatory behaviors in the control of ethanol consumption: a measure of ethanol seeking behavior. Alcohol Clin Exp Res 22: 1783–1787. Sanchis-Segura C, Borchardt T, Vengeliene V, Zghoul T, Bachteler D, Gass P, Sprengel R, Spanagel R (2006) Involvement of the AMPA receptor GluR-C subunit in alcohol-seeking behavior and relapse. J Neurosci 26: 1231–1238. Sanchis-Segura C, Spanagel R (2006) Behavioural assessment of drug reinforcement and addictive features in rodents: an overview. Addict Biol 11: 2–38. Shaham Y, Shalev U, Lu L, de Wit H, Stewart J (2003) The reinstatement model of drug relapse: history, methodology and major findings. Psychopharmacology 168: 3–20. Spanagel R (2009) Alcoholism: a systems approach from molecular physiology to addictive behavior. Physiol Rev 89: 649–705. Stewart J (2003) Stress and relapse to drug seeking: studies in laboratory animals shed light on mechanisms and sources of long-term vulnerability. Am J Addict 12: 1–17. Tsiang MT, Janak PH (2006) Alcohol seeking in C57BL/6 mice induced by conditioned cues and contexts in the extinction-reinstatement model. Alcohol 38: 81–88. Yoneyama N, Crabbe JC, Ford MM, Murillo A, Finn DA (2008) Voluntary ethanol consumption in 22 inbred mouse strains. Alcohol 42: 149–160. Citing Literature Volume35, Issue2February 2011Pages 326-337 ReferencesRelatedInformation
Referência(s)