Evidence map›Paper›PMID 26361221›Full record

ArticlePloS one2015

Exaggerated Nighttime Sleep and Defective Sleep Homeostasis in a Drosophila Knock-In Model of Human Epilepsy.

Emily Petruccelli, Patrick Lansdon, Toshihiro Kitamoto

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Voltage Gated Ion Channels and Sleep.The Journal of membrane biology · 2024
    Review
  4. Article
  5. Frontiers in molecular neuroscience · 2023
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. 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

3 authors at 1 institution in 1 country.

Emily PetruccelliInterdisciplinary Program in Genetics, University of Iowa, Iowa City, IA, United States of America.
Patrick LansdonInterdisciplinary Program in Genetics, University of Iowa, Iowa City, IA, United States of America.
Toshihiro KitamotoInterdisciplinary Program in Genetics, University of Iowa, Iowa City, IA, United States of America; Department of Anesthesia, Carver College of Medicine, University of Iowa, Iowa City, IA, United States of America.
University of Iowa · US

Funding

Interdisciplinary Training Program in Pain ResearchT32NS045549 · NINDS · UNIVERSITY OF IOWA · PI KATHLEEN A SLUKA, Yuriy M Usachev · 2004 to 2026
$3.7M
Studies of genes involved in the lithium responsive neurological processesR01MH085081 · NIMH · UNIVERSITY OF IOWA · PI KITAMOTO, TOSHIHIRO · 2009 to 2013
$1.6M
GPCR-mediated nongenomic steroid actions in control of alcohol-induced behaviorF31AA021625 · NIAAA · UNIVERSITY OF IOWA · PI PETRUCCELLI, EMILY · 2012 to 2014
$86k
NIAAA NIH HHS F31 AA021625NIAAA NIH HHS F31AA021625NIMH NIH HHS R01 MH085081NINDS NIH HHS T32 NS045549NINDS NIH HHS T32NS045549
6 · The paper itself

Abstract

Despite an established link between epilepsy and sleep behavior, it remains unclear how specific epileptogenic mutations affect sleep and subsequently influence seizure susceptibility. Recently, Sun et al. (2012) created a fly knock-in model of human generalized epilepsy with febrile seizures plus (GEFS+), a wide-spectrum disorder characterized by fever-associated seizing in childhood and lifelong affliction. GEFS+ flies carry a disease-causing mutation in their voltage-gated sodium channel (VGSC) gene and display semidominant heat-induced seizing, likely due to reduced GABAergic inhibitory activity at high temperature. Here, we show that at room temperature the GEFS+ mutation dominantly modifies sleep, with mutants exhibiting rapid sleep onset at dusk and increased nighttime sleep as compared to controls. These characteristics of GEFS+ sleep were observed regardless of sex, mating status, and genetic background. GEFS+ mutant sleep phenotypes were more resistant to pharmacologic reduction of GABA transmission by carbamazepine (CBZ) than controls, and were mitigated by reducing GABAA receptor expression specifically in wake-promoting pigment dispersing factor (PDF) neurons. These findings are consistent with increased GABAergic transmission to PDF neurons being mainly responsible for the enhanced nighttime sleep of GEFS+ mutants. Additionally, analyses under other light conditions suggested that the GEFS+ mutation led to reduced buffering of behavioral responses to light on and off stimuli, which contributed to characteristic GEFS+ sleep phenotypes. We further found that GEFS+ mutants had normal circadian rhythms in free-running dark conditions. Interestingly, the mutants lacked a homeostatic rebound following mechanical sleep deprivation, and whereas deprivation treatment increased heat-induced seizure susceptibility in control flies, it unexpectedly reduced seizure activity in GEFS+ mutants. Our study has revealed the sleep architecture of a Drosophila VGSC mutant that harbors a human GEFS+ mutation, and provided unique insight into the relationship between sleep and epilepsy.

Indexed as

HomeostasisPhotoperiodSleep DeprivationAnimalsAnimals, Genetically ModifiedCircadian RhythmDisease Models, AnimalDisease SusceptibilityDrosophila ProteinsEpilepsyEpilepsy, GeneralizedFemalegamma-Aminobutyric AcidHumansMaleMutationDrosophila Proteinsgamma-Aminobutyric AcidRdl protein, DrosophilaReceptors, GABA-A

Identifiers

PMID26361221
PMCPMC4567262
OpenAlexW2179655127

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.