Evidence map›Paper›PMID 25698759›Full record

Trial reportThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Alcohol decreases baseline brain glucose metabolism more in heavy drinkers than controls but has no effect on stimulation-induced metabolic increases.

Nora D Volkow, Gene-Jack Wang, Ehsan Shokri Kojori, Joanna S Fowler, Helene Benveniste, Dardo Tomasi

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.1field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 60 citations in OpenAlex.

  1. Trial
  2. Observational
  3. A ketogenic diet reduces hepatic alcohol metabolism and alcohol consumption in rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Does compulsion explain addiction?Addiction biology · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Neuroimmunometabolism: A New Pathological Nexus Underlying Neurodegenerative Disorders.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Review
  14. EANM procedure guidelines for brain PET imaging using [European journal of nuclear medicine and molecular imaging · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Nora D VolkowNational Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland 20892, nvolkow@nida.nih.gov.
Gene-Jack WangNational Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland 20892.
Ehsan Shokri KojoriNational Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland 20892.
Joanna S FowlerBiosciences Department, Brookhaven National Laboratory, Upton, New York 11973-5000, and.
Helene BenvenisteDepartment of Anesthesiology, Stony Brook Medicine, Stony Brook, New York 11794.ORCID http://orcid.org/0000-0002-2887-6667
Dardo TomasiNational Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland 20892.
National Institute on Alcohol Abuse and Alcoholism · USBrookhaven National Laboratory · USStony Brook Medicine · US

Funding

Neurobiology of Substance Abuse and AddictionZIAAA000550 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI VOLKOW, NORA D. · 2009 to 2025
$115.1M
Intramural NIH HHS
6 · The paper itself

Abstract

During alcohol intoxication, the human brain increases metabolism of acetate and decreases metabolism of glucose as energy substrate. Here we hypothesized that chronic heavy drinking facilitates this energy substrate shift both for baseline and stimulation conditions. To test this hypothesis, we compared the effects of alcohol intoxication (0.75 g/kg alcohol vs placebo) on brain glucose metabolism during video stimulation (VS) versus when given with no stimulation (NS), in 25 heavy drinkers (HDs) and 23 healthy controls, each of whom underwent four PET-(18)FDG scans. We showed that resting whole-brain glucose metabolism (placebo-NS) was lower in HD than controls (13%, p = 0.04); that alcohol (compared with placebo) decreased metabolism more in HD (20 ± 13%) than controls (9 ± 11%, p = 0.005) and in proportion to daily alcohol consumption (r = 0.36, p = 0.01) but found that alcohol did not reduce the metabolic increases in visual cortex from VS in either group. Instead, VS reduced alcohol-induced decreases in whole-brain glucose metabolism (10 ± 12%) compared with NS in both groups (15 ± 13%, p = 0.04), consistent with stimulation-related glucose metabolism enhancement. These findings corroborate our hypothesis that heavy alcohol consumption facilitates use of alternative energy substrates (i.e., acetate) for resting activity during intoxication, which might persist through early sobriety, but indicate that glucose is still favored as energy substrate during brain stimulation. Our findings are consistent with reduced reliance on glucose as the main energy substrate for resting brain metabolism during intoxication (presumably shifting to acetate or other ketones) and a priming of this shift in HDs, which might make them vulnerable to energy deficits during withdrawal.

Indexed as

AdultAlcohol DrinkingAlcoholic IntoxicationBlood PressureBrainBrain MappingCentral Nervous System DepressantsEthanolFemaleFluorodeoxyglucose F18GlucoseHeart RateHumansMalePhotic StimulationPositron-Emission TomographyCentral Nervous System DepressantsEthanolFluorodeoxyglucose F18Glucoseacetate metabolismalcoholismglial metabolismglycolysispositron emission tomography

Identifiers

PMID25698759
PMCPMC4331638
OpenAlexW2044104531

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.