Chronic Ethanol (EtOH) Consumption Differentially Alters Gray and White Matter EtOH Methyl 1H Magnetic Resonance Intensity in the Primate Brain
Background In vivo magnetic resonance spectroscopy (MRS) has previously been used to directly monitor brain ethanol (EtOH). It has been proposed that the EtOH methyl 1H resonance intensity is larger in EtOH‐tolerant individuals than in sensitive individuals. To characterize the relationship between...
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Published in | Alcoholism, clinical and experimental research Vol. 37; no. 8; pp. 1325 - 1332 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.08.2013
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Subjects | |
Online Access | Get full text |
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Abstract | Background
In vivo magnetic resonance spectroscopy (MRS) has previously been used to directly monitor brain ethanol (EtOH). It has been proposed that the EtOH methyl 1H resonance intensity is larger in EtOH‐tolerant individuals than in sensitive individuals. To characterize the relationship between long‐term EtOH exposure and the brain EtOH MRS intensity, we present data from a longitudinal experiment conducted using nonhuman primate subjects.
Methods
In vivo MRS was used to measure the gray matter (GM) and white matter (WM) EtOH methyl 1H MRS intensity in 18 adult male rhesus macaques at 4 time points throughout the course of a chronic drinking experiment. Time points were prior to EtOH drinking, following a 3‐month EtOH induction procedure, and following 6, and 12 subsequent months of 22 h/d of “open access” to EtOH (4% w/v) and water.
Results
The EtOH methyl 1H MRS intensity, which we observed to be independent of age over the range examined, increased with chronic EtOH exposure in GM and WM. In GM, MRS intensity increased from naïve level following the EtOH induction period (90 g/kg cumulative EtOH intake). In WM, MRS intensity was not significantly different from the EtOH‐naïve state until after 6 months of 22‐hour free access (110 to 850 g/kg cumulative intake range). The WM MRS intensity in the EtOH‐naïve state was positively correlated with future drinking, and the increase in WM MRS intensity was negatively correlated with the amount of EtOH consumed throughout the experiment.
Conclusions
Chronic exposure to EtOH is associated with brain changes that result in differential increases in EtOH MRS intensity in GM and WM. The EtOH‐naïve WM MRS intensity pattern is consistent with its previously proposed relationship to innate tolerance to the intoxicating effects of EtOH. EtOH‐dependent MRS intensity changes in GM required less EtOH exposure than was necessary to produce changes in WM. Within WM, an unexpected, potentially age dependent, enhanced sensitivity to EtOH in light drinkers relative to heavy drinkers was observed. |
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AbstractList | In vivo magnetic resonance spectroscopy (MRS) has previously been used to directly monitor brain ethanol (EtOH). It has been proposed that the EtOH methyl ¹H resonance intensity is larger in EtOH-tolerant individuals than in sensitive individuals. To characterize the relationship between long-term EtOH exposure and the brain EtOH MRS intensity, we present data from a longitudinal experiment conducted using nonhuman primate subjects.
In vivo MRS was used to measure the gray matter (GM) and white matter (WM) EtOH methyl ¹H MRS intensity in 18 adult male rhesus macaques at 4 time points throughout the course of a chronic drinking experiment. Time points were prior to EtOH drinking, following a 3-month EtOH induction procedure, and following 6, and 12 subsequent months of 22 h/d of "open access" to EtOH (4% w/v) and water.
The EtOH methyl ¹H MRS intensity, which we observed to be independent of age over the range examined, increased with chronic EtOH exposure in GM and WM. In GM, MRS intensity increased from naïve level following the EtOH induction period (90 g/kg cumulative EtOH intake). In WM, MRS intensity was not significantly different from the EtOH-naïve state until after 6 months of 22-hour free access (110 to 850 g/kg cumulative intake range). The WM MRS intensity in the EtOH-naïve state was positively correlated with future drinking, and the increase in WM MRS intensity was negatively correlated with the amount of EtOH consumed throughout the experiment.
Chronic exposure to EtOH is associated with brain changes that result in differential increases in EtOH MRS intensity in GM and WM. The EtOH-naïve WM MRS intensity pattern is consistent with its previously proposed relationship to innate tolerance to the intoxicating effects of EtOH. EtOH-dependent MRS intensity changes in GM required less EtOH exposure than was necessary to produce changes in WM. Within WM, an unexpected, potentially age dependent, enhanced sensitivity to EtOH in light drinkers relative to heavy drinkers was observed. Background In vivo magnetic resonance spectroscopy (MRS) has previously been used to directly monitor brain ethanol (EtOH). It has been proposed that the EtOH methyl 1H resonance intensity is larger in EtOH‐tolerant individuals than in sensitive individuals. To characterize the relationship between long‐term EtOH exposure and the brain EtOH MRS intensity, we present data from a longitudinal experiment conducted using nonhuman primate subjects. Methods In vivo MRS was used to measure the gray matter (GM) and white matter (WM) EtOH methyl 1H MRS intensity in 18 adult male rhesus macaques at 4 time points throughout the course of a chronic drinking experiment. Time points were prior to EtOH drinking, following a 3‐month EtOH induction procedure, and following 6, and 12 subsequent months of 22 h/d of “open access” to EtOH (4% w/v) and water. Results The EtOH methyl 1H MRS intensity, which we observed to be independent of age over the range examined, increased with chronic EtOH exposure in GM and WM. In GM, MRS intensity increased from naïve level following the EtOH induction period (90 g/kg cumulative EtOH intake). In WM, MRS intensity was not significantly different from the EtOH‐naïve state until after 6 months of 22‐hour free access (110 to 850 g/kg cumulative intake range). The WM MRS intensity in the EtOH‐naïve state was positively correlated with future drinking, and the increase in WM MRS intensity was negatively correlated with the amount of EtOH consumed throughout the experiment. Conclusions Chronic exposure to EtOH is associated with brain changes that result in differential increases in EtOH MRS intensity in GM and WM. The EtOH‐naïve WM MRS intensity pattern is consistent with its previously proposed relationship to innate tolerance to the intoxicating effects of EtOH. EtOH‐dependent MRS intensity changes in GM required less EtOH exposure than was necessary to produce changes in WM. Within WM, an unexpected, potentially age dependent, enhanced sensitivity to EtOH in light drinkers relative to heavy drinkers was observed. In vivo magnetic resonance spectroscopy (MRS) has previously been used to directly monitor brain ethanol (EtOH). It has been proposed that the EtOH methyl 1H resonance intensity is larger in EtOH-tolerant individuals than in sensitive individuals. To characterize the relationship between long-term EtOH exposure and the brain EtOH MRS intensity, we present data from a longitudinal experiment conducted using nonhuman primate subjects. In vivo MRS was used to measure the gray matter (GM) and white matter (WM) EtOH methyl 1H MRS intensity in 18 adult male rhesus macaques at 4 time points throughout the course of a chronic drinking experiment. Time points were prior to EtOH drinking, following a 3-month EtOH induction procedure, and following 6, and 12 subsequent months of 22 h/d of "open access" to EtOH (4% w/v) and water. The EtOH methyl 1H MRS intensity, which we observed to be independent of age over the range examined, increased with chronic EtOH exposure in GM and WM. In GM, MRS intensity increased from naive level following the EtOH induction period (90 g/kg cumulative EtOH intake). In WM, MRS intensity was not significantly different from the EtOH-naive state until after 6 months of 22-hour free access (110 to 850 g/kg cumulative intake range). The WM MRS intensity in the EtOH-naive state was positively correlated with future drinking, and the increase in WM MRS intensity was negatively correlated with the amount of EtOH consumed throughout the experiment. Chronic exposure to EtOH is associated with brain changes that result in differential increases in EtOH MRS intensity in GM and WM. The EtOH-naive WM MRS intensity pattern is consistent with its previously proposed relationship to innate tolerance to the intoxicating effects of EtOH. EtOH-dependent MRS intensity changes in GM required less EtOH exposure than was necessary to produce changes in WM. Within WM, an unexpected, potentially age dependent, enhanced sensitivity to EtOH in light drinkers relative to heavy drinkers was observed. In vivo magnetic resonance spectroscopy (MRS) has previously been used to directly monitor brain ethanol (EtOH). It has been proposed that the EtOH methyl ¹H resonance intensity is larger in EtOH-tolerant individuals than in sensitive individuals. To characterize the relationship between long-term EtOH exposure and the brain EtOH MRS intensity, we present data from a longitudinal experiment conducted using nonhuman primate subjects.BACKGROUNDIn vivo magnetic resonance spectroscopy (MRS) has previously been used to directly monitor brain ethanol (EtOH). It has been proposed that the EtOH methyl ¹H resonance intensity is larger in EtOH-tolerant individuals than in sensitive individuals. To characterize the relationship between long-term EtOH exposure and the brain EtOH MRS intensity, we present data from a longitudinal experiment conducted using nonhuman primate subjects.In vivo MRS was used to measure the gray matter (GM) and white matter (WM) EtOH methyl ¹H MRS intensity in 18 adult male rhesus macaques at 4 time points throughout the course of a chronic drinking experiment. Time points were prior to EtOH drinking, following a 3-month EtOH induction procedure, and following 6, and 12 subsequent months of 22 h/d of "open access" to EtOH (4% w/v) and water.METHODSIn vivo MRS was used to measure the gray matter (GM) and white matter (WM) EtOH methyl ¹H MRS intensity in 18 adult male rhesus macaques at 4 time points throughout the course of a chronic drinking experiment. Time points were prior to EtOH drinking, following a 3-month EtOH induction procedure, and following 6, and 12 subsequent months of 22 h/d of "open access" to EtOH (4% w/v) and water.The EtOH methyl ¹H MRS intensity, which we observed to be independent of age over the range examined, increased with chronic EtOH exposure in GM and WM. In GM, MRS intensity increased from naïve level following the EtOH induction period (90 g/kg cumulative EtOH intake). In WM, MRS intensity was not significantly different from the EtOH-naïve state until after 6 months of 22-hour free access (110 to 850 g/kg cumulative intake range). The WM MRS intensity in the EtOH-naïve state was positively correlated with future drinking, and the increase in WM MRS intensity was negatively correlated with the amount of EtOH consumed throughout the experiment.RESULTSThe EtOH methyl ¹H MRS intensity, which we observed to be independent of age over the range examined, increased with chronic EtOH exposure in GM and WM. In GM, MRS intensity increased from naïve level following the EtOH induction period (90 g/kg cumulative EtOH intake). In WM, MRS intensity was not significantly different from the EtOH-naïve state until after 6 months of 22-hour free access (110 to 850 g/kg cumulative intake range). The WM MRS intensity in the EtOH-naïve state was positively correlated with future drinking, and the increase in WM MRS intensity was negatively correlated with the amount of EtOH consumed throughout the experiment.Chronic exposure to EtOH is associated with brain changes that result in differential increases in EtOH MRS intensity in GM and WM. The EtOH-naïve WM MRS intensity pattern is consistent with its previously proposed relationship to innate tolerance to the intoxicating effects of EtOH. EtOH-dependent MRS intensity changes in GM required less EtOH exposure than was necessary to produce changes in WM. Within WM, an unexpected, potentially age dependent, enhanced sensitivity to EtOH in light drinkers relative to heavy drinkers was observed.CONCLUSIONSChronic exposure to EtOH is associated with brain changes that result in differential increases in EtOH MRS intensity in GM and WM. The EtOH-naïve WM MRS intensity pattern is consistent with its previously proposed relationship to innate tolerance to the intoxicating effects of EtOH. EtOH-dependent MRS intensity changes in GM required less EtOH exposure than was necessary to produce changes in WM. Within WM, an unexpected, potentially age dependent, enhanced sensitivity to EtOH in light drinkers relative to heavy drinkers was observed. |
Author | Flory, Graham S. Rau, Andrew R. Park, Byung Grant, Kathleen A. Shaw, Jessica Kroenke, Christopher D. |
Author_xml | – sequence: 1 givenname: Christopher D. surname: Kroenke fullname: Kroenke, Christopher D. email: kroenkec@ohsu.edu organization: Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Portland, Oregon – sequence: 2 givenname: Graham S. surname: Flory fullname: Flory, Graham S. organization: Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Oregon, Portland – sequence: 3 givenname: Byung surname: Park fullname: Park, Byung organization: Biostatistics Division, Department of Public Health and Preventive Medicine, Oregon Health & Science University, Portland, Oregon – sequence: 4 givenname: Jessica surname: Shaw fullname: Shaw, Jessica organization: Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Oregon, Portland – sequence: 5 givenname: Andrew R. surname: Rau fullname: Rau, Andrew R. organization: Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Oregon, Portland – sequence: 6 givenname: Kathleen A. surname: Grant fullname: Grant, Kathleen A. organization: Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Portland, Oregon |
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Keywords | Self-Administration Ethanol Magnetic Resonance Spectroscopy Gray Matter Nonhuman Primate |
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References | Govindaraju V, Meyerhoff DJ, Maudsley AA, Vermathen M, Weiner MW (1997) Effects of brain membranes on 1H nuclear magnetic resonance signal intensity of ethanol in vitro. Alcohol Alcohol 32:671-681. Chiu TM, Mendelson JH, Sholar MB, Mutschler NH, Wines JD, Hesselbrock VM, Mello NK (2004) Brain alcohol detectability in human subjects with and without a paternal history of alcoholism. J Stud Alcohol 65:16-21. Pfefferbaum A, Lim KO, Zipursky RB, Mathalon DH, Rosenbloom MJ, Lane B, Ha CN, Sullivan EV (1992) Brain gray and white matter volume loss accelerates with aging in chronic alcoholics: a quantitative MRI study. Alcohol Clin Exp Res 16:1078-1089. Bendszus M, Weijers HG, Wiesbeck G, Warmuth-Metz M, Bartsch AJ, Engels S, Boning J, Solymosi L (2001) Sequential MR imaging and proton MR spectroscopy in patients who underwent recent detoxification for chronic alcoholism: correlation with clinical and neuropsychological data. AJNR Am J Neuroradiol 22:1926-1932. Hetherington HP, Mason GF, Pan JW, Ponder SL, Vaughan JT, Twieg DB, Pohost GM (1994) Evaluation of cerebral gray and white matter metabolite differences by spectroscopic imaging at 4.1T. Magn Reson Med 32:565-571. Khanna JM, Le AD, LeBlanc AE, Shah G (1985) Initial sensitivity versus acquired tolerance to ethanol in rats selectively bred for ethanol sensitivity. Psychopharmacology 86:302-306. Spielman DM, Glover GH, Macovski A, Pfefferbaum A (1993) Magnetic resonance spectroscopic imaging of ethanol in the human brain: a feasibility study. Alcohol Clin Exp Res 17:1072-1077. Fein G, Meyerhoff DJ (2000) Ethanol in human brain by magnetic resonance spectroscopy: correlation with blood and breath levels, relaxation, and magnetization transfer. Alcohol Clin Exp Res 24:1227-1235. Lebel C, Walker L, Leemans A, Phillips L, Beaulieu C (2008) Microstructural maturation of the human brain from childhood to adulthood. NeuroImage 40:1044-1055. Hanstock CC, Rothman DL, Shulman RG, Novotny EJ Jr, Petroff OA, Prichard JW (1990) Measurement of ethanol in the human brain using NMR spectroscopy. J Stud Alcohol 51:104-107. Raichle ME, Eichling JO, Straatmann MG, Welch MJ, Larson KB, Ter-Pogossian MM (1976) Blood-brain barrier permeability of 11C-labeled alcohols and 15O-labeled water. Am J Physiol 230:543-552. Chiu TM, Mendelson JH, Woods BT, Teoh SK, Levisohn L, Mello NK (1994) In vivo proton magnetic resonance spectroscopy detection of human alcohol tolerance. Magn Reson Med 32:511-516. Zahr NM, Mayer D, Vinco S, Orduna J, Luong R, Sullivan EV, Pfefferbaum A (2009) In vivo evidence for alcohol-induced neurochemical changes in rat brain without protracted withdrawal, pronounced thiamine deficiency, or severe liver damage. Neuropsychopharmacology 34:1427-1442. Li TK (2000) Pharmacogenetics of responses to alcohol and genes that influence alcohol drinking. J Stud Alcohol 61:5-12. Vivian JA, Green HL, Young JE, Majerksy LS, Thomas BW, Shively CA, Tobin JR, Nader MA, Grant KA (2001) Induction and maintenance of ethanol self-administration in cynomolgus monkeys (Macaca fascicularis): long-term characterization of sex and individual differences. Alcohol Clin Exp Res 25:1087-1097. Meyerhoff DJ, Blumenfeld R, Truran D, Lindgren J, Flenniken D, Cardenas V, Chao LL, Rothlind J, Studholme C, Weiner MW (2004) Effects of heavy drinking, binge drinking, and family history of alcoholism on regional brain metabolites. Alcohol Clin Exp Res 28:650-661. Schweinsburg BC, Alhassoon OM, Taylor MJ, Gonzalez R, Videen JS, Brown GG, Patterson TL, Grant I (2003) Effects of alcoholism and gender on brain metabolism. Am J Psychiatry 160:1180-1183. Quertemont E, Green HL, Grant KA (2003) Brain ethanol concentrations and ethanol discrimination in rats: effects of dose and time. Psychopharmacology 168:262-270. Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Series B 57:289-300. Cuzon Carlson VC, Seabold GK, Helms CM, Garg N, Odagiri M, Rau AR, Daunais J, Alvarez VA, Lovinger DM, Grant KA (2011) Synaptic and morphological neuroadaptations in the putamen associated with long-term, relapsing alcohol drinking in primates. Neuropsychopharmacology 36:2513-2528. Kochunov P, Williamson DE, Lancaster J, Fox P, Cornell J, Blangero J, Glahn DC (2012) Fractional anisotropy of water diffusion in cerebral white matter across the lifespan. Neurobiol Aging 33:9-20. Schuckit MA (2000) Biological phenotypes associated with individuals at high risk for developing alcohol-related disorders. Part 2. Addict Biol 5:23-36. Gomez R, Behar KL, Watzl J, Weinzimer SA, Bulanski B, Sanacora G, Koretski J, Guidone E, Jiang L, Petrakis IL, Pittman B, Krystal JH, Mason GF (2012) Intravenous ethanol infusion decreases human cortical gamma-aminobutyric acid and N-acetylaspartate as measured with proton magnetic resonance spectroscopy at 4 Tesla. Biol Psychiatry 71:239-246. Pietrzykowski AZ, Treistman SN (2008) The molecular basis of tolerance. Alcohol Res Health 31:298-309. Meyerhoff DJ, Rooney WD, Tokumitsu T, Weiner MW (1996) Evidence of multiple ethanol pools in the brain: an in vivo proton magnetization transfer study. Alcohol Clin Exp Res 20:1283-1288. Grant KA, Leng X, Green HL, Szeliga KT, Rogers LS, Gonzales SW (2008) Drinking typography established by scheduled induction predicts chronic heavy drinking in a monkey model of ethanol self-administration. Alcohol Clin Exp Res 32:1824-1838. Adalsteinsson E, Sullivan EV, Mayer D, Pfefferbaum A (2006) In vivo quantification of ethanol kinetics in rat brain. Neuropsychopharmacology 31:2683-2691. Andersen AH, Zhang Z, Zhang M, Gash DM, Avison MJ (1999) Age-associated changes in rhesus CNS composition identified by MRI. Brain Res 829:90-98. Hetherington HP, Telang FW, Pan JW, Sammi MK, Schuhlein D, Molina PE, Volkow ND (1999) Spectroscopic imaging of the uptake kinetics of human brain ethanol. Magn Reson Med 42:1019-1026. Mugler JP 3rd, Brookeman JR (1990) Three-dimensional magnetization-prepared rapid gradient-echo imaging (3D MP RAGE). Magn Reson Med 15:152-157. Taraschi TF, Ellingson JS, Wu A, Zimmerman R, Rubin E (1986) Membrane tolerance to ethanol is rapidly lost after withdrawal: a model for studies of membrane adaptation. Proc Natl Acad Sci USA 83:3669-3673. Flory GS, O'Malley J, Grant KA, Park B, Kroenke CD (2010) Quantification of ethanol methyl (1)H magnetic resonance signal intensity following intravenous ethanol administration in primate brain. Methods 50:189-198. Hetherington HP, Pan JW, Mason GF, Adams D, Vaughn MJ, Twieg DB, Pohost GM (1996) Quantitative 1H spectroscopic imaging of human brain at 4.1 T using image segmentation. Magn Reson Med 36:21-29. Schuckit MA (1994) Low level of response to alcohol as a predictor of future alcoholism. Am J Psychiatry 151:184-189. Moxon LN, Rose SE, Haseler LJ, Galloway GJ, Brereton IM, Bore P, Doddrell DM (1991) The visibility of the 1H NMR signal of ethanol in the dog brain. Magn Reson Med 19:340-348. Mason G, Bendszus M, Meyerhoff D, Hetherington H, Schweinsburg B, Ross B, Taylor M, Krystal J (2005) Magnetic resonance spectroscopic studies of alcoholism: from heavy drinking to alcohol dependence and back again. Alcohol Clin Exp Res 29:150-158. Rooney WD, Johnson G, Li X, Cohen ER, Kim SG, Ugurbil K, Springer CS Jr (2007) Magnetic field and tissue dependencies of human brain longitudinal 1H2O relaxation in vivo. Magn Reson Med 57:308-318. Ellingson JS, Taraschi TF, Wu A, Zimmerman R, Rubin E (1988) Cardiolipin from ethanol-fed rats confers tolerance to ethanol in liver mitochondrial membranes. Proc Natl Acad Sci USA 85:3353-3357. Kaufman MJ, Chiu TM, Mendelson JH, Woods BT, Teoh SK, Eros-Sarnyai M, Mercer G, Mello NK (1996) Brain alcohol detectability increase with repeated administration in humans: a proton spectroscopy study. Magn Reson Med 35:435-440. Harris RA, Trudell JR, Mihic SJ (2008) Ethanol's molecular targets. Sci Signal 1:re7. Petroff OA, Novotny EJ, Ogino T, Avison M, Prichard JW (1990) In vivo measurements of ethanol concentration in rabbit brain by 1H magnetic resonance spectroscopy. J Neurochem 54:1188-1195. Sammi MK, Pan JW, Telang FW, Schuhlein D, Molina PE, Volkow ND, Springer CS, Hetherington HP (2000) Measurements of human brain ethanol T2 by spectroscopic imaging at 4T. Magn Reson Med 44:35-40. Kaufman MJ, Chiu TM, Mendelson JH, Woods BT, Mello NK, Lukas SE, Fivel PA, Wighton LG (1994) In vivo proton magnetic resonance spectroscopy of alcohol in rhesus monkey brain. Magn Reson Imaging 12:1245-1253. Grant KA (1994) Emerging neurochemical concepts in the actions of ethanol at ligand-gated ion channels. Behav Pharmacol 5:383-404. Yuan C, O'Connell RJ, Wilson A, Pietrzykowski AZ, Treistman SN (2008) Acute alcohol tolerance is intrinsic to the BKCa protein, but is modulated by the lipid environment. J Biol Chem 283:5090-5098. Mendelson JH, Woods BT, Chiu TM, Mello NK, Lukas SE, Teoh SK, Sintavanarong P, Cochin J, Hopkins MA, Dobrosielski M (1990) In vivo proton magnetic resonance spectroscopy of alcohol in human brain. Alcohol 7:443-447. 1999; 829 2004; 65 1990; 51 1991; 19 1990; 54 2006; 31 1990; 15 2000; 5 2000; 24 2004; 28 1995; 57 2000; 44 1994; 151 2007 2008; 32 1999; 42 1971 2011; 36 1992; 16 2008; 31 2001; 22 2008; 1 1996; 36 1996; 35 1985; 86 2012; 33 2005; 29 2001; 25 2007; 57 2008; 283 2009; 34 2012; 71 1976; 230 1993; 17 1986; 83 1997; 32 1994; 12 2000; 61 2003; 160 1988; 85 2008; 40 2003; 168 1994; 5 1990; 7 1996; 20 1994; 32 2010; 50 |
References_xml | – reference: Ellingson JS, Taraschi TF, Wu A, Zimmerman R, Rubin E (1988) Cardiolipin from ethanol-fed rats confers tolerance to ethanol in liver mitochondrial membranes. Proc Natl Acad Sci USA 85:3353-3357. – reference: Khanna JM, Le AD, LeBlanc AE, Shah G (1985) Initial sensitivity versus acquired tolerance to ethanol in rats selectively bred for ethanol sensitivity. Psychopharmacology 86:302-306. – reference: Mendelson JH, Woods BT, Chiu TM, Mello NK, Lukas SE, Teoh SK, Sintavanarong P, Cochin J, Hopkins MA, Dobrosielski M (1990) In vivo proton magnetic resonance spectroscopy of alcohol in human brain. Alcohol 7:443-447. – reference: Pietrzykowski AZ, Treistman SN (2008) The molecular basis of tolerance. Alcohol Res Health 31:298-309. – reference: Meyerhoff DJ, Blumenfeld R, Truran D, Lindgren J, Flenniken D, Cardenas V, Chao LL, Rothlind J, Studholme C, Weiner MW (2004) Effects of heavy drinking, binge drinking, and family history of alcoholism on regional brain metabolites. Alcohol Clin Exp Res 28:650-661. – reference: Vivian JA, Green HL, Young JE, Majerksy LS, Thomas BW, Shively CA, Tobin JR, Nader MA, Grant KA (2001) Induction and maintenance of ethanol self-administration in cynomolgus monkeys (Macaca fascicularis): long-term characterization of sex and individual differences. Alcohol Clin Exp Res 25:1087-1097. – reference: Lebel C, Walker L, Leemans A, Phillips L, Beaulieu C (2008) Microstructural maturation of the human brain from childhood to adulthood. NeuroImage 40:1044-1055. – reference: Petroff OA, Novotny EJ, Ogino T, Avison M, Prichard JW (1990) In vivo measurements of ethanol concentration in rabbit brain by 1H magnetic resonance spectroscopy. J Neurochem 54:1188-1195. – reference: Bendszus M, Weijers HG, Wiesbeck G, Warmuth-Metz M, Bartsch AJ, Engels S, Boning J, Solymosi L (2001) Sequential MR imaging and proton MR spectroscopy in patients who underwent recent detoxification for chronic alcoholism: correlation with clinical and neuropsychological data. AJNR Am J Neuroradiol 22:1926-1932. – reference: Andersen AH, Zhang Z, Zhang M, Gash DM, Avison MJ (1999) Age-associated changes in rhesus CNS composition identified by MRI. Brain Res 829:90-98. – reference: Zahr NM, Mayer D, Vinco S, Orduna J, Luong R, Sullivan EV, Pfefferbaum A (2009) In vivo evidence for alcohol-induced neurochemical changes in rat brain without protracted withdrawal, pronounced thiamine deficiency, or severe liver damage. Neuropsychopharmacology 34:1427-1442. – reference: Gomez R, Behar KL, Watzl J, Weinzimer SA, Bulanski B, Sanacora G, Koretski J, Guidone E, Jiang L, Petrakis IL, Pittman B, Krystal JH, Mason GF (2012) Intravenous ethanol infusion decreases human cortical gamma-aminobutyric acid and N-acetylaspartate as measured with proton magnetic resonance spectroscopy at 4 Tesla. Biol Psychiatry 71:239-246. – reference: Adalsteinsson E, Sullivan EV, Mayer D, Pfefferbaum A (2006) In vivo quantification of ethanol kinetics in rat brain. Neuropsychopharmacology 31:2683-2691. – reference: Chiu TM, Mendelson JH, Sholar MB, Mutschler NH, Wines JD, Hesselbrock VM, Mello NK (2004) Brain alcohol detectability in human subjects with and without a paternal history of alcoholism. J Stud Alcohol 65:16-21. – reference: Quertemont E, Green HL, Grant KA (2003) Brain ethanol concentrations and ethanol discrimination in rats: effects of dose and time. Psychopharmacology 168:262-270. – reference: Li TK (2000) Pharmacogenetics of responses to alcohol and genes that influence alcohol drinking. J Stud Alcohol 61:5-12. – reference: Kaufman MJ, Chiu TM, Mendelson JH, Woods BT, Mello NK, Lukas SE, Fivel PA, Wighton LG (1994) In vivo proton magnetic resonance spectroscopy of alcohol in rhesus monkey brain. Magn Reson Imaging 12:1245-1253. – reference: Mason G, Bendszus M, Meyerhoff D, Hetherington H, Schweinsburg B, Ross B, Taylor M, Krystal J (2005) Magnetic resonance spectroscopic studies of alcoholism: from heavy drinking to alcohol dependence and back again. Alcohol Clin Exp Res 29:150-158. – reference: Harris RA, Trudell JR, Mihic SJ (2008) Ethanol's molecular targets. Sci Signal 1:re7. – reference: Taraschi TF, Ellingson JS, Wu A, Zimmerman R, Rubin E (1986) Membrane tolerance to ethanol is rapidly lost after withdrawal: a model for studies of membrane adaptation. Proc Natl Acad Sci USA 83:3669-3673. – reference: Raichle ME, Eichling JO, Straatmann MG, Welch MJ, Larson KB, Ter-Pogossian MM (1976) Blood-brain barrier permeability of 11C-labeled alcohols and 15O-labeled water. Am J Physiol 230:543-552. – reference: Meyerhoff DJ, Rooney WD, Tokumitsu T, Weiner MW (1996) Evidence of multiple ethanol pools in the brain: an in vivo proton magnetization transfer study. Alcohol Clin Exp Res 20:1283-1288. – reference: Fein G, Meyerhoff DJ (2000) Ethanol in human brain by magnetic resonance spectroscopy: correlation with blood and breath levels, relaxation, and magnetization transfer. Alcohol Clin Exp Res 24:1227-1235. – reference: Grant KA, Leng X, Green HL, Szeliga KT, Rogers LS, Gonzales SW (2008) Drinking typography established by scheduled induction predicts chronic heavy drinking in a monkey model of ethanol self-administration. Alcohol Clin Exp Res 32:1824-1838. – reference: Kochunov P, Williamson DE, Lancaster J, Fox P, Cornell J, Blangero J, Glahn DC (2012) Fractional anisotropy of water diffusion in cerebral white matter across the lifespan. Neurobiol Aging 33:9-20. – reference: Hanstock CC, Rothman DL, Shulman RG, Novotny EJ Jr, Petroff OA, Prichard JW (1990) Measurement of ethanol in the human brain using NMR spectroscopy. J Stud Alcohol 51:104-107. – reference: Mugler JP 3rd, Brookeman JR (1990) Three-dimensional magnetization-prepared rapid gradient-echo imaging (3D MP RAGE). Magn Reson Med 15:152-157. – reference: Schuckit MA (2000) Biological phenotypes associated with individuals at high risk for developing alcohol-related disorders. Part 2. Addict Biol 5:23-36. – reference: Hetherington HP, Mason GF, Pan JW, Ponder SL, Vaughan JT, Twieg DB, Pohost GM (1994) Evaluation of cerebral gray and white matter metabolite differences by spectroscopic imaging at 4.1T. Magn Reson Med 32:565-571. – reference: Pfefferbaum A, Lim KO, Zipursky RB, Mathalon DH, Rosenbloom MJ, Lane B, Ha CN, Sullivan EV (1992) Brain gray and white matter volume loss accelerates with aging in chronic alcoholics: a quantitative MRI study. Alcohol Clin Exp Res 16:1078-1089. – reference: Schuckit MA (1994) Low level of response to alcohol as a predictor of future alcoholism. Am J Psychiatry 151:184-189. – reference: Schweinsburg BC, Alhassoon OM, Taylor MJ, Gonzalez R, Videen JS, Brown GG, Patterson TL, Grant I (2003) Effects of alcoholism and gender on brain metabolism. Am J Psychiatry 160:1180-1183. – reference: Cuzon Carlson VC, Seabold GK, Helms CM, Garg N, Odagiri M, Rau AR, Daunais J, Alvarez VA, Lovinger DM, Grant KA (2011) Synaptic and morphological neuroadaptations in the putamen associated with long-term, relapsing alcohol drinking in primates. Neuropsychopharmacology 36:2513-2528. – reference: Hetherington HP, Pan JW, Mason GF, Adams D, Vaughn MJ, Twieg DB, Pohost GM (1996) Quantitative 1H spectroscopic imaging of human brain at 4.1 T using image segmentation. Magn Reson Med 36:21-29. – reference: Chiu TM, Mendelson JH, Woods BT, Teoh SK, Levisohn L, Mello NK (1994) In vivo proton magnetic resonance spectroscopy detection of human alcohol tolerance. Magn Reson Med 32:511-516. – reference: Flory GS, O'Malley J, Grant KA, Park B, Kroenke CD (2010) Quantification of ethanol methyl (1)H magnetic resonance signal intensity following intravenous ethanol administration in primate brain. Methods 50:189-198. – reference: Grant KA (1994) Emerging neurochemical concepts in the actions of ethanol at ligand-gated ion channels. Behav Pharmacol 5:383-404. – reference: Sammi MK, Pan JW, Telang FW, Schuhlein D, Molina PE, Volkow ND, Springer CS, Hetherington HP (2000) Measurements of human brain ethanol T2 by spectroscopic imaging at 4T. Magn Reson Med 44:35-40. – reference: Kaufman MJ, Chiu TM, Mendelson JH, Woods BT, Teoh SK, Eros-Sarnyai M, Mercer G, Mello NK (1996) Brain alcohol detectability increase with repeated administration in humans: a proton spectroscopy study. Magn Reson Med 35:435-440. – reference: Govindaraju V, Meyerhoff DJ, Maudsley AA, Vermathen M, Weiner MW (1997) Effects of brain membranes on 1H nuclear magnetic resonance signal intensity of ethanol in vitro. Alcohol Alcohol 32:671-681. – reference: Moxon LN, Rose SE, Haseler LJ, Galloway GJ, Brereton IM, Bore P, Doddrell DM (1991) The visibility of the 1H NMR signal of ethanol in the dog brain. Magn Reson Med 19:340-348. – reference: Yuan C, O'Connell RJ, Wilson A, Pietrzykowski AZ, Treistman SN (2008) Acute alcohol tolerance is intrinsic to the BKCa protein, but is modulated by the lipid environment. J Biol Chem 283:5090-5098. – reference: Rooney WD, Johnson G, Li X, Cohen ER, Kim SG, Ugurbil K, Springer CS Jr (2007) Magnetic field and tissue dependencies of human brain longitudinal 1H2O relaxation in vivo. Magn Reson Med 57:308-318. – reference: Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Series B 57:289-300. – reference: Hetherington HP, Telang FW, Pan JW, Sammi MK, Schuhlein D, Molina PE, Volkow ND (1999) Spectroscopic imaging of the uptake kinetics of human brain ethanol. Magn Reson Med 42:1019-1026. – reference: Spielman DM, Glover GH, Macovski A, Pfefferbaum A (1993) Magnetic resonance spectroscopic imaging of ethanol in the human brain: a feasibility study. Alcohol Clin Exp Res 17:1072-1077. – volume: 85 start-page: 3353 year: 1988 end-page: 3357 article-title: Cardiolipin from ethanol‐fed rats confers tolerance to ethanol in liver mitochondrial membranes publication-title: Proc Natl Acad Sci USA – volume: 54 start-page: 1188 year: 1990 end-page: 1195 article-title: In vivo measurements of ethanol concentration in rabbit brain by 1H magnetic resonance spectroscopy publication-title: J Neurochem – volume: 71 start-page: 239 year: 2012 end-page: 246 article-title: Intravenous ethanol infusion decreases human cortical gamma‐aminobutyric acid and N‐acetylaspartate as measured with proton magnetic resonance spectroscopy at 4 Tesla publication-title: Biol Psychiatry – volume: 7 start-page: 443 year: 1990 end-page: 447 article-title: In vivo proton magnetic resonance spectroscopy of alcohol in human brain publication-title: Alcohol – volume: 32 start-page: 1824 year: 2008 end-page: 1838 article-title: Drinking typography established by scheduled induction predicts chronic heavy drinking in a monkey model of ethanol self‐administration publication-title: Alcohol Clin Exp Res – volume: 17 start-page: 1072 year: 1993 end-page: 1077 article-title: Magnetic resonance spectroscopic imaging of ethanol in the human brain: a feasibility study publication-title: Alcohol Clin Exp Res – volume: 25 start-page: 1087 year: 2001 end-page: 1097 article-title: Induction and maintenance of ethanol self‐administration in cynomolgus monkeys ( ): long‐term characterization of sex and individual differences publication-title: Alcohol Clin Exp Res – volume: 15 start-page: 152 year: 1990 end-page: 157 article-title: Three‐dimensional magnetization‐prepared rapid gradient‐echo imaging (3D MP RAGE) publication-title: Magn Reson Med – volume: 16 start-page: 1078 year: 1992 end-page: 1089 article-title: Brain gray and white matter volume loss accelerates with aging in chronic alcoholics: a quantitative MRI study publication-title: Alcohol Clin Exp Res – volume: 32 start-page: 511 year: 1994 end-page: 516 article-title: In vivo proton magnetic resonance spectroscopy detection of human alcohol tolerance publication-title: Magn Reson Med – volume: 50 start-page: 189 year: 2010 end-page: 198 article-title: Quantification of ethanol methyl (1)H magnetic resonance signal intensity following intravenous ethanol administration in primate brain publication-title: Methods – volume: 12 start-page: 1245 year: 1994 end-page: 1253 article-title: In vivo proton magnetic resonance spectroscopy of alcohol in rhesus monkey brain publication-title: Magn Reson Imaging – volume: 31 start-page: 298 year: 2008 end-page: 309 article-title: The molecular basis of tolerance publication-title: Alcohol Res Health – year: 2007 – volume: 20 start-page: 1283 year: 1996 end-page: 1288 article-title: Evidence of multiple ethanol pools in the brain: an in vivo proton magnetization transfer study publication-title: Alcohol Clin Exp Res – volume: 24 start-page: 1227 year: 2000 end-page: 1235 article-title: Ethanol in human brain by magnetic resonance spectroscopy: correlation with blood and breath levels, relaxation, and magnetization transfer publication-title: Alcohol Clin Exp Res – volume: 33 start-page: 9 year: 2012 end-page: 20 article-title: Fractional anisotropy of water diffusion in cerebral white matter across the lifespan publication-title: Neurobiol Aging – volume: 57 start-page: 289 year: 1995 end-page: 300 article-title: Controlling the false discovery rate: a practical and powerful approach to multiple testing publication-title: J R Stat Soc Series B – volume: 40 start-page: 1044 year: 2008 end-page: 1055 article-title: Microstructural maturation of the human brain from childhood to adulthood publication-title: NeuroImage – volume: 168 start-page: 262 year: 2003 end-page: 270 article-title: Brain ethanol concentrations and ethanol discrimination in rats: effects of dose and time publication-title: Psychopharmacology – volume: 5 start-page: 23 year: 2000 end-page: 36 article-title: Biological phenotypes associated with individuals at high risk for developing alcohol‐related disorders. Part 2 publication-title: Addict Biol – volume: 160 start-page: 1180 year: 2003 end-page: 1183 article-title: Effects of alcoholism and gender on brain metabolism publication-title: Am J Psychiatry – volume: 829 start-page: 90 year: 1999 end-page: 98 article-title: Age‐associated changes in rhesus CNS composition identified by MRI publication-title: Brain Res – volume: 5 start-page: 383 year: 1994 end-page: 404 article-title: Emerging neurochemical concepts in the actions of ethanol at ligand‐gated ion channels publication-title: Behav Pharmacol – volume: 36 start-page: 21 year: 1996 end-page: 29 article-title: Quantitative 1H spectroscopic imaging of human brain at 4.1 T using image segmentation publication-title: Magn Reson Med – volume: 283 start-page: 5090 year: 2008 end-page: 5098 article-title: Acute alcohol tolerance is intrinsic to the BKCa protein, but is modulated by the lipid environment publication-title: J Biol Chem – volume: 29 start-page: 150 year: 2005 end-page: 158 article-title: Magnetic resonance spectroscopic studies of alcoholism: from heavy drinking to alcohol dependence and back again publication-title: Alcohol Clin Exp Res – volume: 35 start-page: 435 year: 1996 end-page: 440 article-title: Brain alcohol detectability increase with repeated administration in humans: a proton spectroscopy study publication-title: Magn Reson Med – volume: 34 start-page: 1427 year: 2009 end-page: 1442 article-title: In vivo evidence for alcohol‐induced neurochemical changes in rat brain without protracted withdrawal, pronounced thiamine deficiency, or severe liver damage publication-title: Neuropsychopharmacology – start-page: 1 year: 1971 end-page: 62 – volume: 61 start-page: 5 year: 2000 end-page: 12 article-title: Pharmacogenetics of responses to alcohol and genes that influence alcohol drinking publication-title: J Stud Alcohol – volume: 44 start-page: 35 year: 2000 end-page: 40 article-title: Measurements of human brain ethanol T2 by spectroscopic imaging at 4T publication-title: Magn Reson Med – volume: 19 start-page: 340 year: 1991 end-page: 348 article-title: The visibility of the 1H NMR signal of ethanol in the dog brain publication-title: Magn Reson Med – volume: 32 start-page: 565 year: 1994 end-page: 571 article-title: Evaluation of cerebral gray and white matter metabolite differences by spectroscopic imaging at 4.1T publication-title: Magn Reson Med – volume: 57 start-page: 308 year: 2007 end-page: 318 article-title: Magnetic field and tissue dependencies of human brain longitudinal 1H O relaxation in vivo publication-title: Magn Reson Med – volume: 22 start-page: 1926 year: 2001 end-page: 1932 article-title: Sequential MR imaging and proton MR spectroscopy in patients who underwent recent detoxification for chronic alcoholism: correlation with clinical and neuropsychological data publication-title: AJNR Am J Neuroradiol – volume: 65 start-page: 16 year: 2004 end-page: 21 article-title: Brain alcohol detectability in human subjects with and without a paternal history of alcoholism publication-title: J Stud Alcohol – volume: 151 start-page: 184 year: 1994 end-page: 189 article-title: Low level of response to alcohol as a predictor of future alcoholism publication-title: Am J Psychiatry – volume: 83 start-page: 3669 year: 1986 end-page: 3673 article-title: Membrane tolerance to ethanol is rapidly lost after withdrawal: a model for studies of membrane adaptation publication-title: Proc Natl Acad Sci USA – volume: 32 start-page: 671 year: 1997 end-page: 681 article-title: Effects of brain membranes on 1H nuclear magnetic resonance signal intensity of ethanol in vitro publication-title: Alcohol Alcohol – volume: 42 start-page: 1019 year: 1999 end-page: 1026 article-title: Spectroscopic imaging of the uptake kinetics of human brain ethanol publication-title: Magn Reson Med – volume: 36 start-page: 2513 year: 2011 end-page: 2528 article-title: Synaptic and morphological neuroadaptations in the putamen associated with long‐term, relapsing alcohol drinking in primates publication-title: Neuropsychopharmacology – volume: 31 start-page: 2683 year: 2006 end-page: 2691 article-title: In vivo quantification of ethanol kinetics in rat brain publication-title: Neuropsychopharmacology – volume: 1 start-page: re7 year: 2008 article-title: Ethanol's molecular targets publication-title: Sci Signal – volume: 86 start-page: 302 year: 1985 end-page: 306 article-title: Initial sensitivity versus acquired tolerance to ethanol in rats selectively bred for ethanol sensitivity publication-title: Psychopharmacology – volume: 28 start-page: 650 year: 2004 end-page: 661 article-title: Effects of heavy drinking, binge drinking, and family history of alcoholism on regional brain metabolites publication-title: Alcohol Clin Exp Res – volume: 51 start-page: 104 year: 1990 end-page: 107 article-title: Measurement of ethanol in the human brain using NMR spectroscopy publication-title: J Stud Alcohol – volume: 230 start-page: 543 year: 1976 end-page: 552 article-title: Blood‐brain barrier permeability of 11C‐labeled alcohols and 15O‐labeled water publication-title: Am J Physiol |
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In vivo magnetic resonance spectroscopy (MRS) has previously been used to directly monitor brain ethanol (EtOH). It has been proposed that the EtOH... In vivo magnetic resonance spectroscopy (MRS) has previously been used to directly monitor brain ethanol (EtOH). It has been proposed that the EtOH methyl ¹H... In vivo magnetic resonance spectroscopy (MRS) has previously been used to directly monitor brain ethanol (EtOH). It has been proposed that the EtOH methyl 1H... |
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SubjectTerms | Age Alcohol Drinking - metabolism Alcohol-Related Disorders - etiology Animals Brain - drug effects Brain - metabolism Central Nervous System Depressants - metabolism Central Nervous System Depressants - pharmacology Chronic Disease Ethanol Ethanol - metabolism Ethanol - pharmacology Gray Matter Hydrogen Macaca mulatta Magnetic Resonance Spectroscopy Male Nonhuman Primate Self-Administration |
Title | Chronic Ethanol (EtOH) Consumption Differentially Alters Gray and White Matter EtOH Methyl 1H Magnetic Resonance Intensity in the Primate Brain |
URI | https://api.istex.fr/ark:/67375/WNG-ZL1442GC-Q/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1111%2Facer.12097 https://www.ncbi.nlm.nih.gov/pubmed/23550738 https://www.proquest.com/docview/1417531366 https://www.proquest.com/docview/1430862410 |
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