Evidence map›Paper›PMID 41057264›Full record

ArticleeNeuro2025

The Ventral Pallidum Innervates a Distinct Subset of Midbrain Dopamine Neurons.

Olivia J Yang, Hannah B Elam, Kayla Lilly, Alexandra M McCoy, Valeriia Klepikova, Stephanie M Perez, Daniel J Lodge

Abstract read
In one paragraph

Article in eNeuro, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Olivia J YangDepartment of Pharmacology and Center for Biomedical Neuroscience, University of Texas Health Science Center, San Antonio, Texas 78229 yango@livemail.uthscsa.edu.ORCID https://orcid.org/0000-0002-9564-417X
Hannah B ElamDepartment of Pharmacology and Center for Biomedical Neuroscience, University of Texas Health Science Center, San Antonio, Texas 78229.
Kayla LillyDepartment of Pharmacology and Center for Biomedical Neuroscience, University of Texas Health Science Center, San Antonio, Texas 78229.
Alexandra M McCoyDepartment of Pharmacology and Center for Biomedical Neuroscience, University of Texas Health Science Center, San Antonio, Texas 78229.ORCID https://orcid.org/0000-0002-8449-7717
Valeriia KlepikovaDepartment of Pharmacology and Center for Biomedical Neuroscience, University of Texas Health Science Center, San Antonio, Texas 78229.ORCID https://orcid.org/0009-0005-9276-7851
Stephanie M PerezDepartment of Pharmacology and Center for Biomedical Neuroscience, University of Texas Health Science Center, San Antonio, Texas 78229.ORCID https://orcid.org/0000-0002-3258-4456
Daniel J LodgeDepartment of Pharmacology and Center for Biomedical Neuroscience, University of Texas Health Science Center, San Antonio, Texas 78229.ORCID https://orcid.org/0000-0002-6772-1748

Funding

Integrated Graduate Training Program in Neuroscience, UTHSCSAT32NS082145 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI David A Morilak · 2013 to 2026
$1.5M
Aberrant dopamine system function in a rodent model of perimenopause: relevance to psychosisR01AG076030 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Daniel Lodge, Stephanie Marie Perez · 2023 to 2026
$1.3M
Examining orexinergic modulation of the paraventricular nucleus of the thalamus as a novel therapeutic for PTSD and comorbid psychosisF31MH127890 · NIMH · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ELAM, HANNAH · 2022 to 2023
$43k
BLRD VA I01 BX004646BLRD VA I01 BX004693NIA NIH HHS R01 AG076030NIMH NIH HHS F31 MH127890NINDS NIH HHS T32 NS082145
6 · The paper itself

Abstract

Aberrant dopamine transmission is a hallmark of several psychiatric disorders. Dopamine neurons in the ventral tegmental area (VTA) display distinct activity states that are regulated by discrete afferent inputs. For example, burst firing requires excitatory input from the mesopontine tegmentum, while dopamine neuron population activity, defined as the number of spontaneously active dopamine neurons, is thought to be dependent on inhibitory drive from the ventral pallidum (VP). Rodent models used to study psychiatric disorders, such as psychosis, consistently exhibit elevated dopamine neuron population activity, due to decreased tonic inhibition from the VP. However, it remains unclear whether the VP can modulate all dopamine neurons or if only a specific subset of VTA dopamine neurons receive innervation from the VP to be recruited as required. This knowledge is critical for understanding dopamine regulation in normal and pathological conditions. Here, we used in vivo electrophysiology in male and female rats to record VTA dopamine neurons inhibited by electrical stimulation of the VP. Specifically, VP stimulation inhibited ∼22% of spontaneously active dopamine neurons; however, activation of the ventral hippocampus, a modulator of VTA population activity, increased the proportion to ∼48%. This increase suggests that VP selectively modulates a subset of dopamine neurons that can be recruited by afferent activation. Anterograde monosynaptic tracing revealed that approximately half of the VTA dopamine neurons receive input from the VP. Taken together, we demonstrate that a subset of VTA dopamine neurons receives monosynaptic input from the VP, providing valuable information regarding the regulation of VTA neuron activity.

Indexed as

Basal ForebrainDopaminergic NeuronsVentral Tegmental AreaAction PotentialsAnimalsElectric StimulationFemaleHippocampusMaleNeural PathwaysRatsRats, Sprague-Dawleydopaminepsychiatric disordersschizophreniaventral pallidum

Identifiers

PMID41057264
PMCPMC12559842

What OpenQuestion holds

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LicenceCC BY
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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.