Evidence map›Paper›PMID 42049514›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2026

Mechanisms and Cell Type-Dependence of Non-Hebbian Long-Term Potentiation at Primary Afferent Synapses in the Mouse Spinal Superficial Dorsal Horn.

Jie Li, Mark L Baccei

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2026. 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

2 authors.

Jie LiPain Research Center, Department of Anesthesiology, University of Cincinnati Medical Center, Cincinnati, Ohio 45267.
Mark L BacceiPain Research Center, Department of Anesthesiology, University of Cincinnati Medical Center, Cincinnati, Ohio 45267 mark.baccei@uc.edu.ORCID https://orcid.org/0000-0003-3337-7480

Funding

Neuromodulatory regulation of synaptic plasticity in spinal nociceptive circuitsR37NS122141 · NINDS · UNIVERSITY OF CINCINNATI · PI Mark L Baccei · 2022 to 2026
$2.8M
NINDS NIH HHS R37 NS122141
6 · The paper itself

Abstract

Sensory synapses onto ascending spinal projection neurons in the superficial dorsal horn (SDH) can exhibit non-Hebbian plasticity, such as when the firing of primary afferent neurons alone is sufficient to induce long-term potentiation (LTP), following neonatal tissue damage or D1/D5 dopamine receptor activation. However, whether non-Hebbian LTP can be induced at sensory synapses in the absence of tissue injury or exogenous neuromodulatory signaling, the molecular mechanisms underlying this form of synaptic plasticity, and the degree to which non-Hebbian LTP occurs in a cell type-dependent manner within the SDH remain unclear. Here, non-Hebbian plasticity at primary afferent synapses onto lamina I spinoparabrachial neurons, GABAergic (VGAT+) interneurons, and putative glutamatergic (VGAT-) interneurons was examined using ex vivo patch-clamp recordings from the adult mouse SDH of both sexes. Prolonged low-frequency activation of primary afferent inputs evoked non-Hebbian LTP in ascending projection neurons, which reflected an increased probability of presynaptic glutamate release. While the non-Hebbian LTP occurred independently of postsynaptic depolarization, postsynaptic Ca

Indexed as

Long-Term PotentiationNeurons, AfferentPosterior Horn CellsSpinal Cord Dorsal HornSynapsesAnimalsFemaleInterneuronsMaleMiceMice, Inbred C57BLglutamateLTPnociceptionspinal cordspinoparabrachial neuronsynaptic plasticity

Identifiers

PMID42049514
PMCPMC13159437

What OpenQuestion holds

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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.