Evidence map›Paper›PMID 38596834›Full record

ArticleJournal of neurophysiology2024

Comparison of unitary synaptic currents generated by indirect and direct pathway neurons of the mouse striatum.

James A Jones, Jacob Peña, Rostislav I Likhotvorik, Brandon I Garcia-Castañeda, Charles J Wilson

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of neurophysiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

5 authors at 2 institutions in 1 country.

James A JonesDepartment of Neuroscience, Developmental and Regenerative Biology, University of Texas at San Antonio, San Antonio, Texas, United States.ORCID 0000-0001-9836-466X
Jacob PeñaDepartment of Neuroscience, Developmental and Regenerative Biology, University of Texas at San Antonio, San Antonio, Texas, United States.
Rostislav I LikhotvorikDepartment of Neuroscience, Developmental and Regenerative Biology, University of Texas at San Antonio, San Antonio, Texas, United States.ORCID 0000-0001-6218-3832
Brandon I Garcia-CastañedaDepartment of Neuroscience, Developmental and Regenerative Biology, University of Texas at San Antonio, San Antonio, Texas, United States.ORCID 0009-0008-8580-744X
Charles J WilsonDepartment of Neuroscience, Developmental and Regenerative Biology, University of Texas at San Antonio, San Antonio, Texas, United States.ORCID 0000-0002-9004-2145
The University of Texas at San Antonio · USOregon Health & Science University · US

Funding

UTSA RISE Research Training ProgramR25GM060655 · NIGMS · UNIVERSITY OF TEXAS SAN ANTONIO · PI BAREA-RODRIGUEZ, EDWIN J · 2000 to 2022
$21.6M
UTSA Maximizing Access to Research Careers Research Training Program - Admin SupplementT34GM007717 · NIGMS · UNIVERSITY OF TEXAS SAN ANTONIO · PI BAREA-RODRIGUEZ, EDWIN J · 1985 to 2021
$9.5M
Oscillations and Resonance in Basal Ganglia CircuitsR35NS097185 · NINDS · UNIVERSITY OF TEXAS SAN ANTONIO · PI WILSON, CHARLES J · 2017 to 2024
$5.3M
MARC at the University of Texas at San AntonioT34GM145507 · NIGMS · UNIVERSITY OF TEXAS SAN ANTONIO · PI BAREA-RODRIGUEZ, EDWIN J, CASSILL, AARON · 2022 to 2024
$1.5M
Neuron heterogeneity and network dynamic control of synaptic responses in the external globus pallidusF31NS127499 · NINDS · UNIVERSITY OF TEXAS SAN ANTONIO · PI JONES, JAMES · 2022 to 2023
$56k
HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) NS097185HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) NS127499NIGMS NIH HHS R25 GM060655NIGMS NIH HHS T34 GM007717NIGMS NIH HHS T34 GM145507NINDS NIH HHS F31 NS127499NINDS NIH HHS R35 NS097185
6 · The paper itself

Abstract

Two subtypes of striatal spiny projection neurons, iSPNs and dSPNs, whose axons form the "indirect" and "direct" pathways of the basal ganglia, respectively, both make synaptic connections in the external globus pallidus (GPe) but are usually found to have different effects on behavior. Activation of the terminal fields of iSPNs or dSPNs generated compound currents in almost all GPe neurons. To determine whether iSPNs and dSPNs have the same or different effects on pallidal neurons, we studied the unitary synaptic currents generated in GPe neurons by action potentials in single striatal neurons. We used optogenetic excitation to elicit repetitive firing in a small number of nearby SPNs, producing sparse barrages of inhibitory postsynaptic currents (IPSCs) in GPe neurons. From these barrages, we isolated sequences of IPSCs with similar time courses and amplitudes, which presumably arose from the same SPN. There was no difference between the amplitudes of unitary IPSCs generated by the indirect and direct pathways. Most unitary IPSCs were small, but a subset from each pathway were much larger. To determine the effects of these unitary synaptic currents on the action potential firing of GPe neurons, we drove SPNs to fire as before and recorded the membrane potential of GPe neurons. Large unitary potentials from iSPNs and dSPNs perturbed the spike timing of GPe neurons in a similar way. Most SPN-GPe neuron pairs are weakly connected, but a subset of pairs in both pathways are strongly connected.

Indexed as

Inhibitory Postsynaptic PotentialsNeuronsOptogeneticsAction PotentialsAnimalsCorpus StriatumFemaleGlobus PallidusMaleMiceMice, Inbred C57BLNeural PathwaysSynapsesbasal gangliadirect pathwayexternal globus pallidusindirect pathwaystriatum

Identifiers

PMID38596834
PMCPMC11381124
OpenAlexW4394686094

What Socratic 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 Socratic graph.