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Electroacupuncture Reduces Seizure Activity and Enhances GAD 67 and Glutamate Transporter Expression in Kainic Acid Induced Status Epilepticus in Infant Rats

Status epilepticus (SE) is one of the most significant complications in pediatric neurology. Clinical studies have shown positive effects of electroacupuncture (EA) as a therapeutic alternative in the control of partial seizures and secondary generalized clonic seizures. EA promotes the release of n...

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Autores principales: Vega-García, Angelica, Neri-Gómez, Teresa, Buzoianu-Anguiano, Vinnitsa, Guerra-Araiza, Christian, Segura-Uribe, Julia, Feria-Romero, Iris, Orozco-Suarez, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680393/
https://www.ncbi.nlm.nih.gov/pubmed/31252624
http://dx.doi.org/10.3390/bs9070068
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author Vega-García, Angelica
Neri-Gómez, Teresa
Buzoianu-Anguiano, Vinnitsa
Guerra-Araiza, Christian
Segura-Uribe, Julia
Feria-Romero, Iris
Orozco-Suarez, Sandra
author_facet Vega-García, Angelica
Neri-Gómez, Teresa
Buzoianu-Anguiano, Vinnitsa
Guerra-Araiza, Christian
Segura-Uribe, Julia
Feria-Romero, Iris
Orozco-Suarez, Sandra
author_sort Vega-García, Angelica
collection PubMed
description Status epilepticus (SE) is one of the most significant complications in pediatric neurology. Clinical studies have shown positive effects of electroacupuncture (EA) as a therapeutic alternative in the control of partial seizures and secondary generalized clonic seizures. EA promotes the release of neurotransmitters such as GABA and some opioids. The present study aimed to evaluate the anticonvulsive and neuromodulatory effects of Shui Gou DM26 (SG_DM26) acupuncture point electrostimulation on the expression of the glutamate decarboxylase 67 (GAD67) enzyme and the glutamate transporter EAAC1 in an early SE model. At ten postnatal days (10-PD), male rats weighing 22–26 g were divided into 16 groups, including control and treatment groups: Simple stimulation, electrostimulation, anticonvulsant drug treatment, and combined treatment—electrostimulation and pentobarbital (PB). SE was induced with kainic acid (KA), and the following parameters were measured: Motor behavior, and expression of GAD67 and EAAC1. The results suggest an antiepileptic effect derived from SG DM26 point EA. The possible mechanism is most likely the increased production of the inhibitory neurotransmitter GABA, which is observed as an increase in the expression of both GAD67 and EAAC1, as well as the potential synergy between the neuromodulator effects of EA and PB.
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spelling pubmed-66803932019-08-09 Electroacupuncture Reduces Seizure Activity and Enhances GAD 67 and Glutamate Transporter Expression in Kainic Acid Induced Status Epilepticus in Infant Rats Vega-García, Angelica Neri-Gómez, Teresa Buzoianu-Anguiano, Vinnitsa Guerra-Araiza, Christian Segura-Uribe, Julia Feria-Romero, Iris Orozco-Suarez, Sandra Behav Sci (Basel) Article Status epilepticus (SE) is one of the most significant complications in pediatric neurology. Clinical studies have shown positive effects of electroacupuncture (EA) as a therapeutic alternative in the control of partial seizures and secondary generalized clonic seizures. EA promotes the release of neurotransmitters such as GABA and some opioids. The present study aimed to evaluate the anticonvulsive and neuromodulatory effects of Shui Gou DM26 (SG_DM26) acupuncture point electrostimulation on the expression of the glutamate decarboxylase 67 (GAD67) enzyme and the glutamate transporter EAAC1 in an early SE model. At ten postnatal days (10-PD), male rats weighing 22–26 g were divided into 16 groups, including control and treatment groups: Simple stimulation, electrostimulation, anticonvulsant drug treatment, and combined treatment—electrostimulation and pentobarbital (PB). SE was induced with kainic acid (KA), and the following parameters were measured: Motor behavior, and expression of GAD67 and EAAC1. The results suggest an antiepileptic effect derived from SG DM26 point EA. The possible mechanism is most likely the increased production of the inhibitory neurotransmitter GABA, which is observed as an increase in the expression of both GAD67 and EAAC1, as well as the potential synergy between the neuromodulator effects of EA and PB. MDPI 2019-06-27 /pmc/articles/PMC6680393/ /pubmed/31252624 http://dx.doi.org/10.3390/bs9070068 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vega-García, Angelica
Neri-Gómez, Teresa
Buzoianu-Anguiano, Vinnitsa
Guerra-Araiza, Christian
Segura-Uribe, Julia
Feria-Romero, Iris
Orozco-Suarez, Sandra
Electroacupuncture Reduces Seizure Activity and Enhances GAD 67 and Glutamate Transporter Expression in Kainic Acid Induced Status Epilepticus in Infant Rats
title Electroacupuncture Reduces Seizure Activity and Enhances GAD 67 and Glutamate Transporter Expression in Kainic Acid Induced Status Epilepticus in Infant Rats
title_full Electroacupuncture Reduces Seizure Activity and Enhances GAD 67 and Glutamate Transporter Expression in Kainic Acid Induced Status Epilepticus in Infant Rats
title_fullStr Electroacupuncture Reduces Seizure Activity and Enhances GAD 67 and Glutamate Transporter Expression in Kainic Acid Induced Status Epilepticus in Infant Rats
title_full_unstemmed Electroacupuncture Reduces Seizure Activity and Enhances GAD 67 and Glutamate Transporter Expression in Kainic Acid Induced Status Epilepticus in Infant Rats
title_short Electroacupuncture Reduces Seizure Activity and Enhances GAD 67 and Glutamate Transporter Expression in Kainic Acid Induced Status Epilepticus in Infant Rats
title_sort electroacupuncture reduces seizure activity and enhances gad 67 and glutamate transporter expression in kainic acid induced status epilepticus in infant rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680393/
https://www.ncbi.nlm.nih.gov/pubmed/31252624
http://dx.doi.org/10.3390/bs9070068
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