Evidence map›Paper›PMID 33965398›Full record

ReviewNeuropharmacology2021

Contributions of neuroimmune and gut-brain signaling to vulnerability of developing substance use disorders.

Kelsey E Lucerne, Aya Osman, Katherine R Meckel, Drew D Kiraly

Abstract readReview
In one paragraph

Review in Neuropharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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  10. Microbial short-chain fatty acids regulate drug seeking and transcriptional control in a model of cocaine seeking.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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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

4 authors.

Kelsey E LucerneNash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Aya OsmanFriedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Katherine R MeckelNash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Drew D KiralyNash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address: drew.kiraly@mssm.edu.

Funding

Targeting the host metabolome to reverse drug-induced epigenetic changesDP1DA051551 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KIRALY, DREW · 2020 to 2024
$2.8M
Dissecting the role of granulocyte-colony stimulating factor in cocaine-mediated behavioral plasticityK08DA044308 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KIRALY, DREW · 2017 to 2021
$938k
Interneuron and Network Synchrony in Alzheimer's DiseaseR03NS111493 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SHUMAN, TRISTAN · 2019 to 2020
$506k
Neuroimmune modulation of neuronal function during cocaine conditioningR21DA049568 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KIRALY, DREW, SHUMAN, TRISTAN · 2019 to 2020
$466k
NIDA NIH HHS DP1 DA051551NIDA NIH HHS K08 DA044308NIDA NIH HHS R21 DA049568NINDS NIH HHS R03 NS111493
6 · The paper itself

Abstract

Epidemiology and clinical research indicate that only a subset of people who are exposed to drugs of abuse will go on to develop a substance use disorder. Numerous factors impact individual susceptibility to developing a substance use disorder, including intrinsic biological factors, environmental factors, and interpersonal/social factors. Given the extensive morbidity and mortality that is wrought as a consequence of substance use disorders, a substantial body of research has focused on understanding the risk factors that mediate the shift from initial drug use to pathological drug use. Understanding these risk factors provides a clear path for the development of risk mitigation strategies to help reduce the burden of substance use disorders in the population. Here we will review the rapidly growing body of literature that examines the importance of interactions between the peripheral immune system, the gut microbiome, and the central nervous system (CNS) in mediating the transition to pathological drug use. While these systems had long been viewed as distinct, there is growing evidence that there is bidirectional communication between both the immune system and the gut microbiome that drive changes in neural and behavioral plasticity relevant to substance use disorders. Further, both of these systems are highly sensitive to environmental perturbations and are implicated in numerous neuropsychiatric conditions. While the field of study examining these interactions in substance use disorders is in its relative infancy, clarifying the relationship between gut-immune-brain signaling and substance use disorders has potential to improve our understanding of individual propensity to developing addiction and yield important insight into potential treatment options.

Indexed as

Behavior, AddictiveBrainBrain-Gut AxisDysbiosisGastrointestinal MicrobiomeHumansNeuroimmunomodulationSubstance-Related DisordersCytokineMicrobiomeNeuroimmuneOpioidStimulantSubstance use disorder

Identifiers

PMID33965398
PMCPMC8220934

What OpenQuestion holds

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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.