Evidence map›Paper›PMID 35316955›Full record

ArticleFrontiers in behavioral neuroscience2022

Leptin Protects Against the Development and Expression of Cocaine Addiction-Like Behavior in Heterogeneous Stock Rats.

Lieselot L G Carrette, Cristina Corral, Brent Boomhower, Molly Brennan, Caitlin Crook, Clara Ortez, Kokila Shankar, Sierra Simpson, Lisa Maturin, Leah C Solberg Woods and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 18 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

13 authors at 3 institutions in 1 country.

Lieselot L G CarretteDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Cristina CorralDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Brent BoomhowerDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Molly BrennanDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Caitlin CrookDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Clara OrtezDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Kokila ShankarDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Sierra SimpsonDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Lisa MaturinDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Leah C Solberg WoodsDepartment of Internal Medicine, Section on Molecular Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
Abraham A PalmerDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Giordano de GuglielmoDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
Olivier GeorgeDepartment of Psychiatry, University of California, San Diego, La Jolla, CA, United States.
University of California, San Diego · USScripps Research Institute · USWake Forest University · US

Funding

Sequencing CoreP50DA037844 · NIDA · UNIVERSITY OF CHICAGO · PI PALMER, ABRAHAM A · 2014 to 2023
$27.4M
NIDA NIH HHS P50 DA037844
6 · The paper itself

Abstract

Cocaine affects food intake, metabolism and bodyweight. It has been hypothesized that feeding hormones like leptin play a role in this process. Preclinical studies have shown a mutually inhibitory relationship between leptin and cocaine, with leptin also decreasing the rewarding effects of cocaine intake. But prior studies have used relatively small sample sizes and did not investigate individual differences in genetically heterogeneous populations. Here, we examined whether the role of individual differences in bodyweight and blood leptin level are associated with high or low vulnerability to addiction-like behaviors using data from 306 heterogeneous stock rats given extended access to intravenous self-administration of cocaine and 120 blood samples from 60 of these animals, that were stored in the Cocaine Biobank. Finally, we tested a separate cohort to evaluate the causal effect of exogenous leptin administration on cocaine seeking. Bodyweight was reduced due to cocaine self-administration in males during withdrawal and abstinence, but was increased in females during abstinence. However, bodyweight was not correlated with addiction-like behavior vulnerability. Blood leptin levels after ∼6 weeks of cocaine self-administration did not correlate with addiction-like behaviors, however, baseline blood leptin levels before any access to cocaine negatively predicted addiction-like behaviors 6 weeks later. Finally, leptin administration in a separate cohort of 59 animals reduced cocaine seeking in acute withdrawal and after 7 weeks of protracted abstinence. These results demonstrate that high blood leptin level before access to cocaine may be a protective factor against the development of cocaine addiction-like behavior and that exogenous leptin reduces the motivation to take and seek cocaine. On the other hand, these results also show that blood leptin level and bodyweight changes in current users are not relevant biomarkers for addiction-like behaviors.

Indexed as

bodyweighthormonesoutbred strainspsychostimulantsubstance-related disorders

Identifiers

PMID35316955
PMCPMC8934439
OpenAlexW4221025432

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.