Evidence map›Paper›PMID 33935636›Full record

ReviewFrontiers in neuroscience2021

Neuroimmune Mechanisms as Novel Treatment Targets for Substance Use Disorders and Associated Comorbidities.

Mark D Namba, Jonna M Leyrer-Jackson, Erin K Nagy, M Foster Olive, Janet L Neisewander

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Mark D NambaSchool of Life Sciences, Arizona State University, Tempe, AZ, United States.
Jonna M Leyrer-JacksonDepartment of Psychology, Arizona State University, Tempe, AZ, United States.
Erin K NagyDepartment of Psychology, Arizona State University, Tempe, AZ, United States.
M Foster OliveDepartment of Psychology, Arizona State University, Tempe, AZ, United States.
Janet L NeisewanderSchool of Life Sciences, Arizona State University, Tempe, AZ, United States.
Arizona State University · US

Funding

Characterization and reversal of neurocognitive dysfunction produced by long-term synthetic cathinone useR01DA043172 · NIDA · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI OLIVE, M. FOSTER · 2017 to 2021
$1.9M
Brain endorphin targets of low dose alcoholR01AA025590 · NIAAA · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI OLIVE, M. FOSTER · 2016 to 2020
$1.8M
The role of pro-opiomelanocortin neuronal circuitry in mediating ethanol consumptionF32AA027962 · NIAAA · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI JACKSON, JONNA M · 2019 to 2021
$195k
NIAAA NIH HHS F32 AA027962NIAAA NIH HHS R01 AA025590NIDA NIH HHS R01 DA043172
6 · The paper itself

Abstract

Recent studies examining the neurobiology of substance abuse have revealed a significant role of neuroimmune signaling as a mechanism through which drugs of abuse induce aberrant changes in synaptic plasticity and contribute to substance abuse-related behaviors. Immune signaling within the brain and the periphery critically regulates homeostasis of the nervous system. Perturbations in immune signaling can induce neuroinflammation or immunosuppression, which dysregulate nervous system function including neural processes associated with substance use disorders (SUDs). In this review, we discuss the literature that demonstrates a role of neuroimmune signaling in regulating learning, memory, and synaptic plasticity, emphasizing specific cytokine signaling within the central nervous system. We then highlight recent preclinical studies, within the last 5 years when possible, that have identified immune mechanisms within the brain and the periphery associated with addiction-related behaviors. Findings thus far underscore the need for future investigations into the clinical potential of immunopharmacology as a novel approach toward treating SUDs. Considering the high prevalence rate of comorbidities among those with SUDs, we also discuss neuroimmune mechanisms of common comorbidities associated with SUDs and highlight potentially novel treatment targets for these comorbid conditions. We argue that immunopharmacology represents a novel frontier in the development of new pharmacotherapies that promote long-term abstinence from drug use and minimize the detrimental impact of SUD comorbidities on patient health and treatment outcomes.

Indexed as

addictionchronic painHIVMDDneuroinflammationPTSD

Identifiers

PMID33935636
PMCPMC8082184
OpenAlexW3153566969

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.