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A Selective Histamine H4 Receptor Antagonist, JNJ7777120, Role on glutamate Transporter Activity in Chronic Depression
Glutamate release and reuptake play a key role in the pathophysiology of depression. glutamatergic nerves in the hippocampus region are modulated by histaminergic afferents. Excessive accumulation of glutamate in the synaptic area causes degeneration of neuron cells. The H4 receptor is defined as th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880293/ https://www.ncbi.nlm.nih.gov/pubmed/35207733 http://dx.doi.org/10.3390/jpm12020246 |
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author | Yeni, Yesim Cakir, Zeynep Hacimuftuoglu, Ahmet Taghizadehghalehjoughi, Ali Okkay, Ufuk Genc, Sidika Yildirim, Serkan Saglam, Yavuz Selim Calina, Daniela Tsatsakis, Aristidis Docea, Anca Oana |
author_facet | Yeni, Yesim Cakir, Zeynep Hacimuftuoglu, Ahmet Taghizadehghalehjoughi, Ali Okkay, Ufuk Genc, Sidika Yildirim, Serkan Saglam, Yavuz Selim Calina, Daniela Tsatsakis, Aristidis Docea, Anca Oana |
author_sort | Yeni, Yesim |
collection | PubMed |
description | Glutamate release and reuptake play a key role in the pathophysiology of depression. glutamatergic nerves in the hippocampus region are modulated by histaminergic afferents. Excessive accumulation of glutamate in the synaptic area causes degeneration of neuron cells. The H4 receptor is defined as the main immune system histamine receptor with a pro-inflammatory role. To understand the role of this receptor, the drug JNJ7777120 was used to reveal the chronic depression-glutamate relationship. We have important findings showing that the H4 antagonist increases the glutamate transporters’ instantaneous activity. In our experiment, it has been shown that blocking the H4 receptor leads to increased neuron cell viability and improvement in behavioral ability due to glutamate. Therefore, JNJ can be used to prevent neurotoxicity, inhibit membrane phospholipase activation and free radical formation, and minimize membrane disruption. In line with our findings, results have been obtained that indicate that JNJ will contribute to the effective prevention and treatment of depression. |
format | Online Article Text |
id | pubmed-8880293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88802932022-02-26 A Selective Histamine H4 Receptor Antagonist, JNJ7777120, Role on glutamate Transporter Activity in Chronic Depression Yeni, Yesim Cakir, Zeynep Hacimuftuoglu, Ahmet Taghizadehghalehjoughi, Ali Okkay, Ufuk Genc, Sidika Yildirim, Serkan Saglam, Yavuz Selim Calina, Daniela Tsatsakis, Aristidis Docea, Anca Oana J Pers Med Article Glutamate release and reuptake play a key role in the pathophysiology of depression. glutamatergic nerves in the hippocampus region are modulated by histaminergic afferents. Excessive accumulation of glutamate in the synaptic area causes degeneration of neuron cells. The H4 receptor is defined as the main immune system histamine receptor with a pro-inflammatory role. To understand the role of this receptor, the drug JNJ7777120 was used to reveal the chronic depression-glutamate relationship. We have important findings showing that the H4 antagonist increases the glutamate transporters’ instantaneous activity. In our experiment, it has been shown that blocking the H4 receptor leads to increased neuron cell viability and improvement in behavioral ability due to glutamate. Therefore, JNJ can be used to prevent neurotoxicity, inhibit membrane phospholipase activation and free radical formation, and minimize membrane disruption. In line with our findings, results have been obtained that indicate that JNJ will contribute to the effective prevention and treatment of depression. MDPI 2022-02-09 /pmc/articles/PMC8880293/ /pubmed/35207733 http://dx.doi.org/10.3390/jpm12020246 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yeni, Yesim Cakir, Zeynep Hacimuftuoglu, Ahmet Taghizadehghalehjoughi, Ali Okkay, Ufuk Genc, Sidika Yildirim, Serkan Saglam, Yavuz Selim Calina, Daniela Tsatsakis, Aristidis Docea, Anca Oana A Selective Histamine H4 Receptor Antagonist, JNJ7777120, Role on glutamate Transporter Activity in Chronic Depression |
title | A Selective Histamine H4 Receptor Antagonist, JNJ7777120, Role on glutamate Transporter Activity in Chronic Depression |
title_full | A Selective Histamine H4 Receptor Antagonist, JNJ7777120, Role on glutamate Transporter Activity in Chronic Depression |
title_fullStr | A Selective Histamine H4 Receptor Antagonist, JNJ7777120, Role on glutamate Transporter Activity in Chronic Depression |
title_full_unstemmed | A Selective Histamine H4 Receptor Antagonist, JNJ7777120, Role on glutamate Transporter Activity in Chronic Depression |
title_short | A Selective Histamine H4 Receptor Antagonist, JNJ7777120, Role on glutamate Transporter Activity in Chronic Depression |
title_sort | selective histamine h4 receptor antagonist, jnj7777120, role on glutamate transporter activity in chronic depression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880293/ https://www.ncbi.nlm.nih.gov/pubmed/35207733 http://dx.doi.org/10.3390/jpm12020246 |
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