Literature DB >> 27378279

The effect of early life status epilepticus on ultrasonic vocalizations in mice.

Conner D Reynolds1, Gregory Smith2, Taylor Jefferson1, Joaquin N Lugo1,2.   

Abstract

OBJECTIVE: Infant crying is a series of innate vocal patterns intended to elicit the attention of adult caregivers for fulfillment of specific needs such as pain, hunger, or hypostimulation. It is one of the earliest forms of observable communication. In neonatal rodents, this behavior has recently been investigated as a potential early behavioral marker of neural deficits in neurodevelopmental disorders. However, few studies have examined the effects of seizures on vocalization behavior during the neonatal period. The purpose of this study is to investigate the effect of a single kainate-induced early life seizure on vocalization behavior in mice. This study also investigates the subsequent effect of seizures on two pathways critical for early neural development and epileptogenesis: the phosphoinositide 3-kinase|serine/threonine kinase|mammalian target of rapamycin (PI3K-Akt-mTOR) and canonical (Wingless-Int Wnt) intracellular signaling pathways.
METHODS: On postnatal day 10, male and female 129SvEvTac mice received a single intraperitoneal injection of kainic acid (2.5 mg/kg) or vehicle injection. The kainate administration resulted in 1-2 h of status epilepticus. On postnatal days 11 and 12, the quantity and duration of isolation-induced ultrasonic vocalizations were recorded. Western blotting analyses were performed using male and female pups on postnatal day 12.
RESULTS: There was significant, male-specific suppression in the quantity and total duration of 50-kHz calls on postnatal day 12 following seizures. The hippocampi of male mice on this postnatal day also revealed male-specific changes in the PI3K-Akt-mTOR intracellular signaling pathway, as well as changes in phosphorylated fragile × mental retardation protein. SIGNIFICANCE: These findings demonstrate that early life seizures can disrupt communication behavior in neonatal mice. Wiley Periodicals, Inc.
© 2016 International League Against Epilepsy.

Entities:  

Keywords:  Epilepsy; Isolation-induced vocalizations; Mammalian target of rapamycin; Neurodevelopmental disorder; Phosphoinositide 3-kinase; Ultrasonic vocalization

Mesh:

Substances:

Year:  2016        PMID: 27378279      PMCID: PMC5335835          DOI: 10.1111/epi.13450

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  34 in total

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5.  Effects of experience and context on 50-kHz vocalizations in rats.

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8.  Comprehensive analysis of ultrasonic vocalizations in a mouse model of fragile X syndrome reveals limited, call type specific deficits.

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9.  The interaction between early life epilepsy and autistic-like behavioral consequences: a role for the mammalian target of rapamycin (mTOR) pathway.

Authors:  Delia M Talos; Hongyu Sun; Xiangping Zhou; Erin C Fitzgerald; Michele C Jackson; Peter M Klein; Victor J Lan; Annelise Joseph; Frances E Jensen
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Authors:  Markus Wöhr; Rainer K W Schwarting
Journal:  PLoS One       Date:  2007-12-26       Impact factor: 3.240

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1.  High seizure load during sensitive periods of development leads to broad shifts in ultrasonic vocalization behavior in neonatal male and female C57BL/6J mice.

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2.  Early-life status epilepticus acutely impacts select quantitative and qualitative features of neonatal vocalization behavior: Spectrographic and temporal characterizations in C57BL/6 mice.

Authors:  Conner D Reynolds; Suzanne O Nolan; Jessica L Huebschman; Samantha L Hodges; Joaquin N Lugo
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3.  A single early-life seizure results in long-term behavioral changes in the adult Fmr1 knockout mouse.

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4.  Rapamycin, but not minocycline, significantly alters ultrasonic vocalization behavior in C57BL/6J pups in a flurothyl seizure model.

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5.  Dataset on sociability, cognitive function, gene and protein expression of molecules involved in social behavior, reward system and synapse function following early-life status epilepticus in Wistar rats.

Authors:  Ana Miriã Pacífico; Samuel P Batista; Fernanda T Ribeiro; Pedro B Dos Santos; Gabriel Bruno Silveira; Bruna Pascarelli Pedrico do Nascimento; Eduardo Dias Junior; Geraldo Henrique L Barbosa; Miriam Oliveira Ribeiro; Sergio Gomes da Silva; Roberta M Cysneiros
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6.  Increased Endocannabinoid Signaling Reduces Social Motivation in Intact Rats and Does Not Affect Animals Submitted to Early-Life Seizures.

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