Evidence map›Paper›PMID 32078631›Full record

ArticlePLoS biology2020

A wake-active locomotion circuit depolarizes a sleep-active neuron to switch on sleep.

Elisabeth Maluck, Inka Busack, Judith Besseling, Florentin Masurat, Michal Turek, Karl Emanuel Busch, Henrik Bringmann

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Science advances · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Sleep Analysis in AdultThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  9. Article
  10. Melatonin promotes sleep by activating the BK channel inProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  11. Behavioral States.Genetics · 2020
    Review
  12. Worms sleep: a perspective.Journal of neurogenetics
    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

7 authors at 3 institutions in 2 countries.

Elisabeth MaluckMax Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Inka BusackMax Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Judith BesselingMax Planck Institute for Biophysical Chemistry, Göttingen, Germany.ORCID 0000-0001-6879-2700
Florentin MasuratMax Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Michal TurekMax Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Karl Emanuel BuschUniversity of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0001-7886-3226
Henrik BringmannMax Planck Institute for Biophysical Chemistry, Göttingen, Germany.ORCID 0000-0002-7689-8617
Max Planck Institute for Biophysical Chemistry · DEPhilipps University of Marburg · DEUniversity of Edinburgh · GB

Funding

Medical Research Council MR/N004574/1
6 · The paper itself

Abstract

Sleep-active neurons depolarize during sleep to suppress wakefulness circuits. Wake-active wake-promoting neurons in turn shut down sleep-active neurons, thus forming a bipartite flip-flop switch. However, how sleep is switched on is unclear because it is not known how wakefulness is translated into sleep-active neuron depolarization when the system is set to sleep. Using optogenetics in Caenorhabditis elegans, we solved the presynaptic circuit for depolarization of the sleep-active RIS neuron during developmentally regulated sleep, also known as lethargus. Surprisingly, we found that RIS activation requires neurons that have known roles in wakefulness and locomotion behavior. The RIM interneurons-which are active during and can induce reverse locomotion-play a complex role and can act as inhibitors of RIS when they are strongly depolarized and as activators of RIS when they are modestly depolarized. The PVC command interneurons, which are known to promote forward locomotion during wakefulness, act as major activators of RIS. The properties of these locomotion neurons are modulated during lethargus. The RIMs become less excitable. The PVCs become resistant to inhibition and have an increased capacity to activate RIS. Separate activation of neither the PVCs nor the RIMs appears to be sufficient for sleep induction; instead, our data suggest that they act in concert to activate RIS. Forward and reverse circuit activity is normally mutually exclusive. Our data suggest that RIS may be activated at the transition between forward and reverse locomotion states, perhaps when both forward (PVC) and reverse (including RIM) circuit activity overlap. While RIS is not strongly activated outside of lethargus, altered activity of the locomotion interneurons during lethargus favors strong RIS activation and thus sleep. The control of sleep-active neurons by locomotion circuits suggests that sleep control may have evolved from locomotion control. The flip-flop sleep switch in C. elegans thus requires an additional component, wake-active sleep-promoting neurons that translate wakefulness into the depolarization of a sleep-active neuron when the worm is sleepy. Wake-active sleep-promoting circuits may also be required for sleep state switching in other animals, including in mammals.

Indexed as

AnimalsArousalBehavior, AnimalCaenorhabditis elegansCaenorhabditis elegans ProteinsCalciumHomeostasisInterneuronsLarvaLocomotionNeural PathwaysNeuronsOptogeneticsSleep StagesWakefulnessCaenorhabditis elegans ProteinsCalcium

Identifiers

PMID32078631
PMCPMC7053779
OpenAlexW3008498562

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.