A Two-Hit Approach Inducing Flurothyl Seizures in Fmr1 Knockout Mice Impacts Anxiety and Repetitive Behaviors

Fragile X Syndrome (FXS) is the leading monogenetic cause of autism spectrum disorder (ASD) and is associated with seizures. We examined the impact of repeated seizures on the behavioral and molecular changes in male Fmr1 knockout (KO) mice and wild-type (WT) mice. Seizures were induced by administe...

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Published in:Brain sciences Vol. 14; no. 9; p. 892
Main Authors: Blandin, Katherine J, Narvaiz, David A, Sullens, Donald Gregory, Womble, Paige D, Hodges, Samantha L, Binder, Matthew S, Faust, Amanda, Nguyen, Phuoc H, Pranske, Zachary J, Lugo, Joaquin N
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Abstract Fragile X Syndrome (FXS) is the leading monogenetic cause of autism spectrum disorder (ASD) and is associated with seizures. We examined the impact of repeated seizures on the behavioral and molecular changes in male Fmr1 knockout (KO) mice and wild-type (WT) mice. Seizures were induced by administering three flurothyl seizures per day across postnatal days (PD) 7-11, for a total of 15 seizures. In adulthood, mice were tested in a battery of behavioral tasks to assess long-term behavioral deficits. The two-hit impact of a Fmr1 knockout and seizures resulted in decreased anxiety-like behavior in the elevated plus maze test and a longer latency to their first nose poke (repetitive behavior). Seizures resulted in decreased activity, decreased repetitive behavior (grooming and rearings), and decreased social behavior, while they also increased habituation to auditory stimuli and increased freezing in delayed fear conditioning in both KO and control mice. KO mice displayed increased repetitive behavior in the open field task (clockwise revolutions) and repeated nose pokes, and decreased anxiety in the open field test. No differences in mTOR signaling were found. These findings further illuminate the long-term effects of synergistic impact of two hits on the developing brain.
AbstractList Background: Fragile X Syndrome (FXS) is the leading monogenetic cause of autism spectrum disorder (ASD) and is associated with seizures. We examined the impact of repeated seizures on the behavioral and molecular changes in male Fmr1 knockout (KO) mice and wild-type (WT) mice. Methods: Seizures were induced by administering three flurothyl seizures per day across postnatal days (PD) 7–11, for a total of 15 seizures. In adulthood, mice were tested in a battery of behavioral tasks to assess long-term behavioral deficits. Results: The two-hit impact of a Fmr1 knockout and seizures resulted in decreased anxiety-like behavior in the elevated plus maze test and a longer latency to their first nose poke (repetitive behavior). Seizures resulted in decreased activity, decreased repetitive behavior (grooming and rearings), and decreased social behavior, while they also increased habituation to auditory stimuli and increased freezing in delayed fear conditioning in both KO and control mice. KO mice displayed increased repetitive behavior in the open field task (clockwise revolutions) and repeated nose pokes, and decreased anxiety in the open field test. No differences in mTOR signaling were found. Conclusions: These findings further illuminate the long-term effects of synergistic impact of two hits on the developing brain.
Fragile X Syndrome (FXS) is the leading monogenetic cause of autism spectrum disorder (ASD) and is associated with seizures. We examined the impact of repeated seizures on the behavioral and molecular changes in male Fmr1 knockout (KO) mice and wild-type (WT) mice. Seizures were induced by administering three flurothyl seizures per day across postnatal days (PD) 7-11, for a total of 15 seizures. In adulthood, mice were tested in a battery of behavioral tasks to assess long-term behavioral deficits. The two-hit impact of a Fmr1 knockout and seizures resulted in decreased anxiety-like behavior in the elevated plus maze test and a longer latency to their first nose poke (repetitive behavior). Seizures resulted in decreased activity, decreased repetitive behavior (grooming and rearings), and decreased social behavior, while they also increased habituation to auditory stimuli and increased freezing in delayed fear conditioning in both KO and control mice. KO mice displayed increased repetitive behavior in the open field task (clockwise revolutions) and repeated nose pokes, and decreased anxiety in the open field test. No differences in mTOR signaling were found. These findings further illuminate the long-term effects of synergistic impact of two hits on the developing brain.
Fragile X Syndrome (FXS) is the leading monogenetic cause of autism spectrum disorder (ASD) and is associated with seizures. We examined the impact of repeated seizures on the behavioral and molecular changes in male Fmr1 knockout (KO) mice and wild-type (WT) mice.BACKGROUNDFragile X Syndrome (FXS) is the leading monogenetic cause of autism spectrum disorder (ASD) and is associated with seizures. We examined the impact of repeated seizures on the behavioral and molecular changes in male Fmr1 knockout (KO) mice and wild-type (WT) mice.Seizures were induced by administering three flurothyl seizures per day across postnatal days (PD) 7-11, for a total of 15 seizures. In adulthood, mice were tested in a battery of behavioral tasks to assess long-term behavioral deficits.METHODSSeizures were induced by administering three flurothyl seizures per day across postnatal days (PD) 7-11, for a total of 15 seizures. In adulthood, mice were tested in a battery of behavioral tasks to assess long-term behavioral deficits.The two-hit impact of a Fmr1 knockout and seizures resulted in decreased anxiety-like behavior in the elevated plus maze test and a longer latency to their first nose poke (repetitive behavior). Seizures resulted in decreased activity, decreased repetitive behavior (grooming and rearings), and decreased social behavior, while they also increased habituation to auditory stimuli and increased freezing in delayed fear conditioning in both KO and control mice. KO mice displayed increased repetitive behavior in the open field task (clockwise revolutions) and repeated nose pokes, and decreased anxiety in the open field test. No differences in mTOR signaling were found.RESULTSThe two-hit impact of a Fmr1 knockout and seizures resulted in decreased anxiety-like behavior in the elevated plus maze test and a longer latency to their first nose poke (repetitive behavior). Seizures resulted in decreased activity, decreased repetitive behavior (grooming and rearings), and decreased social behavior, while they also increased habituation to auditory stimuli and increased freezing in delayed fear conditioning in both KO and control mice. KO mice displayed increased repetitive behavior in the open field task (clockwise revolutions) and repeated nose pokes, and decreased anxiety in the open field test. No differences in mTOR signaling were found.These findings further illuminate the long-term effects of synergistic impact of two hits on the developing brain.CONCLUSIONSThese findings further illuminate the long-term effects of synergistic impact of two hits on the developing brain.
Audience Academic
Author Binder, Matthew S
Womble, Paige D
Hodges, Samantha L
Lugo, Joaquin N
Narvaiz, David A
Sullens, Donald Gregory
Faust, Amanda
Blandin, Katherine J
Pranske, Zachary J
Nguyen, Phuoc H
AuthorAffiliation 4 Department of Neuroscience, University of Maryland, Baltimore, MD 20742, USA; phuoc.nguyen@som.umaryland.edu
3 Department of Neurosurgery, Yale University School of Medicine, East Haven, CT 06520, USA; mbinder@trinity.edu
2 Department of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48109, USA; hodgessamantha6@gmail.com
7 Institute of Biomedical Studies, Baylor University, Waco, TX 76798, USA
6 Department of Biology, Baylor University, Waco, TX 76798, USA
5 Department of Biology, Brandeis University, Waltham, MA 02453, USA; zpranske@brandeis.edu
1 Department of Psychology and Neuroscience, Baylor University, Waco, TX 76798, USA; katie_blandin1@baylor.edu (K.J.B.); david_narvaiz1@baylor.edu (D.A.N.); paigedeannwomble@gmail.com (P.D.W.)
AuthorAffiliation_xml – name: 7 Institute of Biomedical Studies, Baylor University, Waco, TX 76798, USA
– name: 1 Department of Psychology and Neuroscience, Baylor University, Waco, TX 76798, USA; katie_blandin1@baylor.edu (K.J.B.); david_narvaiz1@baylor.edu (D.A.N.); paigedeannwomble@gmail.com (P.D.W.)
– name: 4 Department of Neuroscience, University of Maryland, Baltimore, MD 20742, USA; phuoc.nguyen@som.umaryland.edu
– name: 2 Department of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48109, USA; hodgessamantha6@gmail.com
– name: 3 Department of Neurosurgery, Yale University School of Medicine, East Haven, CT 06520, USA; mbinder@trinity.edu
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developmental epilepsy
double-hit
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Snippet Fragile X Syndrome (FXS) is the leading monogenetic cause of autism spectrum disorder (ASD) and is associated with seizures. We examined the impact of repeated...
Background: Fragile X Syndrome (FXS) is the leading monogenetic cause of autism spectrum disorder (ASD) and is associated with seizures. We examined the impact...
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StartPage 892
SubjectTerms Anxiety
Auditory stimuli
Autism
Behavior
Convulsions & seizures
developmental epilepsy
double-hit
early life seizures
Epilepsy
Ethylenediaminetetraacetic acid
Fear conditioning
Flurothyl
FMR1 protein
Fragile X syndrome
Grooming
Habituation
Hyperactivity
Intellectual disabilities
Kinases
Laboratory animals
Latency
Long-term effects
mTOR
Nose
Open-field behavior
Seizures
Seizures (Medicine)
Social aspects
Social behavior
Tonic immobility
TOR protein
two-hit
X chromosomes
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Title A Two-Hit Approach Inducing Flurothyl Seizures in Fmr1 Knockout Mice Impacts Anxiety and Repetitive Behaviors
URI https://www.ncbi.nlm.nih.gov/pubmed/39335388
https://www.proquest.com/docview/3110383896
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Volume 14
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