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 |
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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. |
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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 – name: 5 Department of Biology, Brandeis University, Waltham, MA 02453, USA; zpranske@brandeis.edu – name: 6 Department of Biology, Baylor University, Waco, TX 76798, USA |
Author_xml | – sequence: 1 givenname: Katherine J surname: Blandin fullname: Blandin, Katherine J organization: Department of Psychology and Neuroscience, Baylor University, Waco, TX 76798, USA – sequence: 2 givenname: David A surname: Narvaiz fullname: Narvaiz, David A organization: Department of Psychology and Neuroscience, Baylor University, Waco, TX 76798, USA – sequence: 3 givenname: Donald Gregory orcidid: 0000-0002-6426-2355 surname: Sullens fullname: Sullens, Donald Gregory organization: Department of Psychology and Neuroscience, Baylor University, Waco, TX 76798, USA – sequence: 4 givenname: Paige D orcidid: 0000-0003-0999-1050 surname: Womble fullname: Womble, Paige D organization: Department of Psychology and Neuroscience, Baylor University, Waco, TX 76798, USA – sequence: 5 givenname: Samantha L surname: Hodges fullname: Hodges, Samantha L organization: Department of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48109, USA – sequence: 6 givenname: Matthew S surname: Binder fullname: Binder, Matthew S organization: Department of Neurosurgery, Yale University School of Medicine, East Haven, CT 06520, USA – sequence: 7 givenname: Amanda orcidid: 0009-0003-1801-6801 surname: Faust fullname: Faust, Amanda organization: Department of Psychology and Neuroscience, Baylor University, Waco, TX 76798, USA – sequence: 8 givenname: Phuoc H surname: Nguyen fullname: Nguyen, Phuoc H organization: Department of Neuroscience, University of Maryland, Baltimore, MD 20742, USA – sequence: 9 givenname: Zachary J orcidid: 0000-0001-9364-622X surname: Pranske fullname: Pranske, Zachary J organization: Department of Biology, Brandeis University, Waltham, MA 02453, USA – sequence: 10 givenname: Joaquin N orcidid: 0000-0001-6874-8718 surname: Lugo fullname: Lugo, Joaquin N organization: Institute of Biomedical Studies, Baylor University, Waco, TX 76798, USA |
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Keywords | epilepsy early life seizures mTOR developmental epilepsy double-hit two-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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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 |
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