Evidence map›Paper›PMID 29163075›Full record

ReviewFrontiers in systems neuroscience2017

Pauses in Striatal Cholinergic Interneurons: What is Revealed by Their Common Themes and Variations?

Yan-Feng Zhang, Stephanie J Cragg

Abstract readReview
In one paragraph

Review in Frontiers in systems neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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  17. Striatal Cholinergic Signaling in Time and Space.Molecules (Basel, Switzerland) · 2022
    Review
  18. Article
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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

2 authors.

Yan-Feng ZhangDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Stephanie J CraggDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.

Funding

Medical Research Council G0700932Medical Research Council MR/J004324/1Medical Research Council MR/K013866/1Parkinson's UK G-0803Parkinson's UK G-0808Parkinson's UK G-1103Parkinson's UK G-1305Parkinson's UK G-1504Parkinson's UK H-1003Parkinson's UK J-0901
6 · The paper itself

Abstract

Striatal cholinergic interneurons, the so-called tonically active neurons (TANs), pause their firing in response to sensory cues and rewards during classical conditioning and instrumental tasks. The respective pause responses observed can demonstrate many commonalities, such as constant latency and duration, synchronous occurrence in a population of cells, and coincidence with phasic activities of midbrain dopamine neurons (DANs) that signal reward predictions and errors. Pauses can however also show divergent properties. Pause latencies and durations can differ in a given TAN between appetitive vs. aversive outcomes in classical conditioning, initial excitation can be present or absent, and a second pause can variably follow a rebound. Despite more than 20 years of study, the functions of these pause responses are still elusive. Our understanding of pause function is hindered by an incomplete understanding of how pauses are generated. In this mini-review article, we compare pause types, as well as current key hypotheses for inputs underlying pauses that include dopamine-induced inhibition through D

Indexed as

cholinergic interneuroncortexdopaminepause responsestriatumthalamustonically active neuron

Identifiers

PMID29163075
PMCPMC5670143

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.