Evidence map›Paper›PMID 30074236›Full record

ArticleThe Journal of physiology2018

A simple decision to move in response to touch reveals basic sensory memory and mechanisms for variable response times.

Stella Koutsikou, Robert Merrison-Hort, Edgar Buhl, Andrea Ferrario, Wen-Chang Li, Roman Borisyuk, Stephen R Soffe, Alan Roberts

Abstract read
In one paragraph

Article in The Journal of physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  5. The early development and physiology ofJournal of neurophysiology · 2021
    Article
  6. Article
  7. Review
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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

8 authors.

Stella KoutsikouSchool of Biological Sciences, University of Bristol, 24 Tyndall Avenue, Bristol, BS8 1TQ, UK.ORCID 0000-0003-2933-3637
Robert Merrison-HortSchool of Computing, Electronics and Mathematics, University of Plymouth, Drake Circus, Plymouth, PL4 8AA, UK.ORCID 0000-0001-8215-7527
Edgar BuhlSchool of Biological Sciences, University of Bristol, 24 Tyndall Avenue, Bristol, BS8 1TQ, UK.ORCID 0000-0003-1274-5870
Andrea FerrarioSchool of Computing, Electronics and Mathematics, University of Plymouth, Drake Circus, Plymouth, PL4 8AA, UK.
Wen-Chang LiSchool of Psychology and Neuroscience, University of St Andrews, 9 South Street, St Andrews, Fife, KY16 9JP, UK.
Roman BorisyukSchool of Computing, Electronics and Mathematics, University of Plymouth, Drake Circus, Plymouth, PL4 8AA, UK.
Stephen R SoffeSchool of Biological Sciences, University of Bristol, 24 Tyndall Avenue, Bristol, BS8 1TQ, UK.
Alan RobertsSchool of Biological Sciences, University of Bristol, 24 Tyndall Avenue, Bristol, BS8 1TQ, UK.

Funding

Biotechnology and the Biological Sciences Research Council BB/L000814/1Biotechnology and the Biological Sciences Research Council BB/L00111X/1Biotechnology and the Biological Sciences Research Council BB/L002353/1
6 · The paper itself

Abstract

key pointsShort-term working memory and decision-making are usually studied in the cerebral cortex; in many models of simple decision making, sensory signals build slowly and noisily to threshold to initiate a motor response after long, variable delays. When touched, hatchling frog tadpoles decide whether to swim; we define the long and variable delays to swimming and use whole-cell recordings to uncover the neurons and processes responsible. Firing in sensory and sensory pathway neurons is short latency, and too brief and invariant to explain these delays, while recordings from hindbrain reticulospinal neurons controlling swimming reveal a prolonged and variable build-up of synaptic excitation which can reach firing threshold and initiate swimming. We propose this excitation provides a sensory memory of the stimulus and may be generated by small reverberatory hindbrain networks. Our results uncover fundamental network mechanisms that allow animals to remember brief sensory stimuli and delay simple motor decisions. ABSTRACT: Many motor responses to sensory input, like locomotion or eye movements, are much slower than reflexes. Can simpler animals provide fundamental answers about the cellular mechanisms for motor decisions? Can we observe the 'accumulation' of excitation to threshold proposed to underlie decision making elsewhere? We explore how somatosensory touch stimulation leads to the decision to swim in hatchling Xenopus tadpoles. Delays measured to swimming in behaving and immobilised tadpoles are long and variable. Activity in their extensively studied sensory and sensory pathway neurons is too short-lived to explain these response delays. Instead, whole-cell recordings from the hindbrain reticulospinal neurons that drive swimming show that these receive prolonged, variable synaptic excitation lasting for nearly a second following a brief stimulus. They fire and initiate swimming when this excitation reaches threshold. Analysis of the summation of excitation requires us to propose extended firing in currently undefined presynaptic hindbrain neurons. Simple models show that a small excitatory recurrent-network inserted in the sensory pathway can mimic this process. We suggest that such a network may generate slow, variable summation of excitation to threshold. This excitation provides a simple memory of the sensory stimulus. It allows temporal and spatial integration of sensory inputs and explains the long, variable delays to swimming. The process resembles the 'accumulation' of excitation proposed for cortical circuits in mammals. We conclude that fundamental elements of sensory memory and decision making are present in the brainstem at a surprisingly early stage in development.

Indexed as

AnimalsElectrophysiological PhenomenaExcitatory Postsynaptic PotentialsLarvaMemoryModels, BiologicalNeuronsPatch-Clamp TechniquesReaction TimeSwimmingTouchVideo RecordingXenopus laevisDecision-makingLocomotionReticulospinal neuronsSomatosensoryXenopus laevis

Identifiers

PMID30074236
PMCPMC6292811

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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.