Evidence map›Paper›PMID 39300273›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2025

Role of serotonin neurons in the dorsal raphe nucleus in heroin self-administration and punishment.

Chen Li, Nicholas S McCloskey, Saadet Inan, Lynn G Kirby

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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.

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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.

Chen LiCenter for Substance Abuse Research, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.ORCID http://orcid.org/0009-0001-0671-3904
Nicholas S McCloskeyCenter for Substance Abuse Research, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Saadet InanCenter for Substance Abuse Research, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Lynn G KirbyCenter for Substance Abuse Research, Lewis Katz School of Medicine at Temple University, Philadelphia, USA. lkirby@temple.edu.ORCID http://orcid.org/0000-0001-5684-6716

Funding

Pilot Projects Core (PPC)P30DA013429 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI SCOTT M. RAWLS · 2000 to 2026
$34.6M
Regulation of 5-HT circuits by CRF and GABA in opioid addiction and stress-induced relapseR01DA045771 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI KIRBY, LYNN G · 2019 to 2023
$1.9M
NIDA NIH HHS P30 DA013429NIDA NIH HHS R01 DA045771U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) DA045771
6 · The paper itself

Abstract

One hallmark of substance use disorder is continued drug use despite negative consequences. When drug-taking behavior is punished with aversive stimuli, i.e. footshock, rats can also be categorized into punishment-resistant or compulsive vs. punishment-sensitive or non-compulsive phenotypes. The serotonin (5-hydroxytryptamine, 5-HT) system modulates responses to both reward and punishment. The goal of the current study was to examine punishment phenotypes in heroin self-administration and to determine the role of dorsal raphe nucleus (DRN) 5-HT neurons in both basal and punished heroin self-administration. First, rats were exposed to punished heroin self-administration and neuronal excitability of DRN 5-HT neurons was compared between punishment-resistant and punishment-sensitive phenotypes using ex vivo electrophysiology. Second, DRN 5-HT neuronal activity was manipulated in vivo during basal and punished heroin self-administration using chemogenetic tools in a Tph2-iCre rat line. While rats separated into punishment-resistant and punishment-sensitive phenotypes for punished heroin self-administration, DRN 5-HT neuronal excitability did not differ between the phenotypes. While chemogenetic inhibition of DRN 5-HT neurons was without effect, chemogenetic activation of DRN 5-HT neurons increased both basal and punished heroin self-administration selectively in punishment-resistant animals. Additionally, the responsiveness to chemogenetic activation of DRN 5-HT neurons in basal self-administration and motivation for heroin in progressive ratio each predicted resistance to punishment. Therefore, our data support the role for the DRN 5-HT system in compulsive heroin self-administration.

Indexed as

Dorsal Raphe NucleusHeroinNarcoticsPunishmentSerotonergic NeuronsAnimalsMaleRatsRats, TransgenicSelf AdministrationTryptophan HydroxylaseHeroinNarcoticstph2 protein, ratTryptophan Hydroxylase

Identifiers

PMID39300273
PMCPMC11735851

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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.