Nakul R. Raval, Kelly Smart, Gustavo A. Angarita, Rachel Miller, Yiyun Huang, John H. Krystal, Richard E. Carson, Kelly P. Cosgrove, Stephanie S. O'Malley, Ansel T. Hillmer
{"title":"用代谢性谷氨酸受体5正电子发射断层扫描测量急性酒精诱导的变化","authors":"Nakul R. Raval, Kelly Smart, Gustavo A. Angarita, Rachel Miller, Yiyun Huang, John H. Krystal, Richard E. Carson, Kelly P. Cosgrove, Stephanie S. O'Malley, Ansel T. Hillmer","doi":"10.1111/adb.70031","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Alcohol consumption at clinically relevant doses alters brain glutamate release. However, few techniques exist to measure these changes in humans. The metabotropic glutamate receptor 5 (mGluR5) PET radioligand [<sup>11</sup>C]ABP688 is sensitive to acute alcohol in rodents, possibly mediated by alcohol effects on glutamate release. This study aimed to determine the sensitivity of [<sup>11</sup>C]ABP688 PET to an acute alcohol challenge in humans.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Eight social drinkers (25–42 years; 5 females) with a recent drinking occasion achieving a blood alcohol level (BAL) > 80 mg/dL were recruited. All participants underwent a 90-min dynamic baseline [<sup>11</sup>C]ABP688 PET scan. Two weeks later (range: 7–29 days), participants completed an oral laboratory alcohol challenge over 30 min, targeting a BAL of 60 mg/dL. Immediately after the challenge, a second [<sup>11</sup>C]ABP688 PET scan was performed. Non-displaceable binding potential (<i>BP</i><sub>ND</sub>; indicative of mGluR5 availability) and <i>R</i><sub>1</sub> (indicative of relative blood flow) were estimated using the simplified reference tissue model with the cerebellum as the reference region. Blood samples were taken throughout the scanning procedure to measure the BAL.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Seven participants (4 females) completed the study. The mean peak BAL achieved was 61 ± 18 mg/dL. Acute alcohol significantly decreased [<sup>11</sup>C]ABP688 <i>BP</i><sub>ND</sub>, <i>F</i>(1, 42) = 17.05, <i>p</i> < 0.001, Cohen's <i>d</i> = 0.32–0.60, and increased [<sup>11</sup>C]ABP688 <i>R</i><sub>1</sub>, <i>F</i>(1, 42) = 6.67, <i>p</i> = 0.013, Cohen's <i>d</i> = 0.32–0.48, across brain regions. Exploratory analysis showed a positive relationship between alcohol-induced % change in [<sup>11</sup>C]ABP688 <i>R</i><sub>1</sub> in cortical regions and peak BAL (Spearman rho = 0.78 [frontal cortex] and 0.85 [temporal cortex] = 0.024 and 0.011).</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>This proof-of-concept study demonstrates that [<sup>11</sup>C]ABP688 PET imaging is sensitive to the effects of acute alcohol consumption. The observed decrease in mGluR5 availability aligns with preclinical data potentially indicating acute increased extracellular glutamate concentrations following ethanol dosing. This imaging tool could be useful for future investigations into the acute effects of alcohol on the brain during abstinence and withdrawal.</p>\n </section>\n </div>","PeriodicalId":7289,"journal":{"name":"Addiction Biology","volume":"30 5","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/adb.70031","citationCount":"0","resultStr":"{\"title\":\"Acute Alcohol-Induced Changes Measured With Metabotropic Glutamate Receptor 5 Positron Emission Tomography\",\"authors\":\"Nakul R. Raval, Kelly Smart, Gustavo A. Angarita, Rachel Miller, Yiyun Huang, John H. Krystal, Richard E. Carson, Kelly P. Cosgrove, Stephanie S. O'Malley, Ansel T. Hillmer\",\"doi\":\"10.1111/adb.70031\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Alcohol consumption at clinically relevant doses alters brain glutamate release. However, few techniques exist to measure these changes in humans. The metabotropic glutamate receptor 5 (mGluR5) PET radioligand [<sup>11</sup>C]ABP688 is sensitive to acute alcohol in rodents, possibly mediated by alcohol effects on glutamate release. This study aimed to determine the sensitivity of [<sup>11</sup>C]ABP688 PET to an acute alcohol challenge in humans.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Eight social drinkers (25–42 years; 5 females) with a recent drinking occasion achieving a blood alcohol level (BAL) > 80 mg/dL were recruited. All participants underwent a 90-min dynamic baseline [<sup>11</sup>C]ABP688 PET scan. Two weeks later (range: 7–29 days), participants completed an oral laboratory alcohol challenge over 30 min, targeting a BAL of 60 mg/dL. Immediately after the challenge, a second [<sup>11</sup>C]ABP688 PET scan was performed. Non-displaceable binding potential (<i>BP</i><sub>ND</sub>; indicative of mGluR5 availability) and <i>R</i><sub>1</sub> (indicative of relative blood flow) were estimated using the simplified reference tissue model with the cerebellum as the reference region. Blood samples were taken throughout the scanning procedure to measure the BAL.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Seven participants (4 females) completed the study. The mean peak BAL achieved was 61 ± 18 mg/dL. Acute alcohol significantly decreased [<sup>11</sup>C]ABP688 <i>BP</i><sub>ND</sub>, <i>F</i>(1, 42) = 17.05, <i>p</i> < 0.001, Cohen's <i>d</i> = 0.32–0.60, and increased [<sup>11</sup>C]ABP688 <i>R</i><sub>1</sub>, <i>F</i>(1, 42) = 6.67, <i>p</i> = 0.013, Cohen's <i>d</i> = 0.32–0.48, across brain regions. Exploratory analysis showed a positive relationship between alcohol-induced % change in [<sup>11</sup>C]ABP688 <i>R</i><sub>1</sub> in cortical regions and peak BAL (Spearman rho = 0.78 [frontal cortex] and 0.85 [temporal cortex] = 0.024 and 0.011).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>This proof-of-concept study demonstrates that [<sup>11</sup>C]ABP688 PET imaging is sensitive to the effects of acute alcohol consumption. The observed decrease in mGluR5 availability aligns with preclinical data potentially indicating acute increased extracellular glutamate concentrations following ethanol dosing. This imaging tool could be useful for future investigations into the acute effects of alcohol on the brain during abstinence and withdrawal.</p>\\n </section>\\n </div>\",\"PeriodicalId\":7289,\"journal\":{\"name\":\"Addiction Biology\",\"volume\":\"30 5\",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/adb.70031\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Addiction Biology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/adb.70031\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Addiction Biology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/adb.70031","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Alcohol consumption at clinically relevant doses alters brain glutamate release. However, few techniques exist to measure these changes in humans. The metabotropic glutamate receptor 5 (mGluR5) PET radioligand [11C]ABP688 is sensitive to acute alcohol in rodents, possibly mediated by alcohol effects on glutamate release. This study aimed to determine the sensitivity of [11C]ABP688 PET to an acute alcohol challenge in humans.
Methods
Eight social drinkers (25–42 years; 5 females) with a recent drinking occasion achieving a blood alcohol level (BAL) > 80 mg/dL were recruited. All participants underwent a 90-min dynamic baseline [11C]ABP688 PET scan. Two weeks later (range: 7–29 days), participants completed an oral laboratory alcohol challenge over 30 min, targeting a BAL of 60 mg/dL. Immediately after the challenge, a second [11C]ABP688 PET scan was performed. Non-displaceable binding potential (BPND; indicative of mGluR5 availability) and R1 (indicative of relative blood flow) were estimated using the simplified reference tissue model with the cerebellum as the reference region. Blood samples were taken throughout the scanning procedure to measure the BAL.
Results
Seven participants (4 females) completed the study. The mean peak BAL achieved was 61 ± 18 mg/dL. Acute alcohol significantly decreased [11C]ABP688 BPND, F(1, 42) = 17.05, p < 0.001, Cohen's d = 0.32–0.60, and increased [11C]ABP688 R1, F(1, 42) = 6.67, p = 0.013, Cohen's d = 0.32–0.48, across brain regions. Exploratory analysis showed a positive relationship between alcohol-induced % change in [11C]ABP688 R1 in cortical regions and peak BAL (Spearman rho = 0.78 [frontal cortex] and 0.85 [temporal cortex] = 0.024 and 0.011).
Conclusions
This proof-of-concept study demonstrates that [11C]ABP688 PET imaging is sensitive to the effects of acute alcohol consumption. The observed decrease in mGluR5 availability aligns with preclinical data potentially indicating acute increased extracellular glutamate concentrations following ethanol dosing. This imaging tool could be useful for future investigations into the acute effects of alcohol on the brain during abstinence and withdrawal.
期刊介绍：
Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields.
Addiction Biology includes peer-reviewed original research reports and reviews.
Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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