Evidence map›Paper›PMID 40478894›Full record

ArticlePloS one2025

Cocaine self-administration attenuates brain glucose metabolism and functional connectivity in rats.

Christopher Rowan, Colin Hanna, Munawwar Sajjad, Rutao Yao, Alireza Sharafsha, Kai-Uwe Lewandrowski, Kenneth Blum, Albert Pinhasov, Panayotis K Thanos

Erratum issuedAbstract read
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Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Christopher RowanBehavioral Neuropharmacology and Neuroimaging Laboratory on Addictions, Clinical Research Institute on Addictions, Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biosciences, State University of New York at Buffalo, Buffalo, New York, United States of America.
Colin HannaBehavioral Neuropharmacology and Neuroimaging Laboratory on Addictions, Clinical Research Institute on Addictions, Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biosciences, State University of New York at Buffalo, Buffalo, New York, United States of America.
Munawwar SajjadDepartment of Nuclear Medicine, University at Buffalo, Buffalo, United States of America.
Rutao YaoDepartment of Nuclear Medicine, University at Buffalo, Buffalo, United States of America.
Alireza SharafshaCellular and Molecular Research Center, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran.ORCID 0000-0001-8048-9587
Kai-Uwe LewandrowskiDepartment of Orthopaedics, Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0001-7842-2914
Kenneth BlumCenter for Sports, Exercise, and Mental Health, Western University Health Sciences, Pomona, California, United States of America.
Albert PinhasovDepartment of Molecular Biology, Adelson School of Medicine, Ariel University, Ariel, Israel.ORCID 0000-0001-8116-4565
Panayotis K ThanosBehavioral Neuropharmacology and Neuroimaging Laboratory on Addictions, Clinical Research Institute on Addictions, Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biosciences, State University of New York at Buffalo, Buffalo, New York, United States of America.ORCID 0000-0001-9784-731X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCocaine abuse and Cocaine Use Disorder (CUD) is an increasingly urgent public health issue leading to major health risks often resulting in a decreased lifespan and quality of life. Previous human research has described brain function of cocaine addicts however the amount of cocaine use, duration of use, and exclusion of using other drugs (i.e., nicotine and alcohol) have all been difficult to control. One unanswered question is related to how does cocaine affect both brain glucose metabolism and functional connectivity?.

methodsThe present study examined using positron emission tomography (PET) imaging and the glucose analog [18F]-Fluorodeoxyglucose (18F-FDG), brain glucose metabolism (BGluM) and functional connectivity in male rats (N = 6) that self-administered cocaine compared to baseline control scans in the same animals prior to cocaine exposure.

resultsOur Results showed that Cocaine Self-Administration (CSA) caused significant BGluM decreases in several brain regions including posterior thalamic nuclei, Claustrum (Cl); Solitary nucleus, Presubiculum (PrS); Caudate Putamen (CPu); Anterior hypothalamic area (AHA); Ventral pallidum (VP); and amygdala. Activation (increased BGluM) was observed in the primary somatosensory cortex. These regions are associated with memory, spatial navigation, visual processing and saliency along with other somatosensory and motor functions, as well as regulatory autonomic function (cardiovascular) and hormonal response.

conclusionThis brain functional connectivity mapping illustrated a brain circuit composed of brain regions that are either a part of or connect with the mesolimbic reward pathway that is mediated by dopamine. When this circuit is dysregulated, it is believed to be associated with substance use disorders and reward dysregulation which have recently been described as attributes of preaddiction.

Indexed as

BrainCocaineGlucoseAnimalsCocaine-Related DisordersFluorodeoxyglucose F18MalePositron-Emission TomographyRatsRats, Sprague-DawleySelf AdministrationCocaineFluorodeoxyglucose F18Glucose

Identifiers

PMID40478894
PMCPMC12143558

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Registered trials

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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.