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.
Journal article
Exaggerated Nighttime Sleep and Defective Sleep Homeostasis in a Drosophila Knock-In Model of Human Epilepsy
PLoS One, Vol.10(9), p.0137758
09/11/2015
DOI: 10.1371/journal.pone.0137758
PMCID: PMC4567262
PMID: 26361221
Abstract
Details
- Title: Subtitle
- Exaggerated Nighttime Sleep and Defective Sleep Homeostasis in a Drosophila Knock-In Model of Human Epilepsy
- Creators
- Emily Petruccelli - University of IowaPatrick Lansdon - University of IowaToshihiro Kitamoto - University of Iowa
- Resource Type
- Journal article
- Publication Details
- PLoS One, Vol.10(9), p.0137758
- DOI
- 10.1371/journal.pone.0137758
- PMID
- 26361221
- PMCID
- PMC4567262
- ISSN
- 1932-6203
- eISSN
- 1932-6203
- Copyright
- © 2015 Petruccelli et al.
- Grant note
- Funding provided by National Institutes of Health (http://www.nih.gov/), Iowa Center for Research by Undergraduates (http://www.uiowa.edu/icru/), NIAAA F31AA021625 (EP), NINDS T32NS045549 (PL), NIMH R01 MH085081 (TK). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
- Language
- English
- Date published
- 09/11/2015
- Academic Unit
- Anesthesia; Neuroscience and Pharmacology; Interdisciplinary Graduate Program in Genetics
- Record Identifier
- 9983557487402771
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