Evidence map›Paper›PMID 19906875›Full record

ArticleJournal of neurophysiology2010

Involvement of reactive oxygen species in long-term potentiation in the spinal cord dorsal horn.

Kwan Yeop Lee, Kyungsoon Chung, Jin Mo Chung

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
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  7. Spinal antinociceptive effect of the PnTx4(5-5) peptide is possibly mediated by the NMDA autoreceptors.The journal of venomous animals and toxins including tropical diseases · 2024
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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

3 authors at 1 institution in 1 country.

Kwan Yeop LeeDepartment of Neuroscience and Cell Biology, University of Texas Medical Branch, 310 University Blvd., Galveston, TX 77555-1069, USA.
Kyungsoon Chung
Jin Mo Chung
The University of Texas Medical Branch at Galveston · US

Funding

VISCERAL PAINP01NS011255 · NINDS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI HULSEBOSCH, CLAIRE E · 1985 to 2012
$13.6M
Mechanisms of Neuropathic PainR01NS031680 · NINDS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI CHUNG, JIN M · 1994 to 2016
$4.1M
NINDS NIH HHS P01 NS011255NINDS NIH HHS P01 NS-11255NINDS NIH HHS R01 NS031680NINDS NIH HHS R01 NS-31680
6 · The paper itself

Abstract

Recent studies suggest that reactive oxygen species (ROS) are functional messenger molecules in central sensitization, an underlying mechanism of persistent pain. Because spinal cord long-term potentiation (LTP) is the electrophysiological basis of central sensitization, this study investigates the effects of the increased or decreased spinal ROS levels on spinal cord LTP. Spinal cord LTP is induced by either brief, high-frequency stimulation (HFS) of a dorsal root at C-fiber intensity or superfusion of a ROS donor, tert-butyl hydroperoxide (t-BOOH), onto rat spinal cord slice preparations. Field excitatory postsynaptic potentials (fEPSPs) evoked by dorsal root stimulations with either Abeta- or C-fiber intensity are recorded from the superficial dorsal horn. HFS significantly increases the slope of both Abeta- and C-fiber evoked fEPSPs, thus suggesting LTP development. The induction, not the maintenance, of HFS-induced LTP is blocked by a N-methyl-D-aspartate (NMDA) receptor antagonist, D-2-amino-5-phosphonopentanoic acid (D-AP5). Both the induction and maintenance of LTP of Abeta-fiber-evoked fEPSPs are inhibited by a ROS scavenger, either N-tert-butyl-alpha-phenylnitrone or 4-hydroxy-2,2,6,6-tetramethylpiperidine-N-oxyl. A ROS donor, t-BOOH-induced LTP is inhibited by N-tert-butyl-alpha-phenylnitrone but not by D-AP5. Furthermore, HFS-induced LTP and t-BOOH-induced LTP occlude each other. The data suggest that elevated ROS is a downstream event of NMDA receptor activation and an essential step for potentiation of synaptic excitability in the spinal dorsal horn.

Indexed as

2-Amino-5-phosphonovalerateAnimalsCentral Nervous System AgentsCyclic N-OxidesEvoked PotentialsExcitatory Amino Acid AntagonistsExcitatory Postsynaptic PotentialsFree Radical ScavengersIn Vitro TechniquesLong-Term PotentiationMaleNerve Fibers, MyelinatedNerve Fibers, UnmyelinatedPosterior Horn CellsRatsRats, Sprague-Dawley2-Amino-5-phosphonovalerateCentral Nervous System AgentsCyclic N-OxidesExcitatory Amino Acid AntagonistsFree Radical Scavengersphenyl-N-tert-butylnitroneReactive Oxygen SpeciesReceptors, N-Methyl-D-AspartateSpin Labelstempoltert-Butylhydroperoxide

Identifiers

PMID19906875
PMCPMC2807226
OpenAlexW2169057285

What OpenQuestion holds

Textmetadata
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.