Chronic stress intensify PTZ-induced seizures by triggering neuroinflammation and oxidative stress

Epilepsy is a paroxysmal abnormal hypersynchronous electrical discharge characterized by recurrent seizures. It affects more than 50 million people worldwide. Stress is the leading cause of neurodegeneration and can produce seizures that may lead to or aggravate epilepsy. Inflammation plays a vital...

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Veröffentlicht in:Biochemical and biophysical research communications 2024-10, Vol.729, p.150333, Article 150333
Hauptverfasser: Khan, Jehan Zeb, Zainab, Syeda Rida, Rehman, Mujeeb Ur, Abid, Muhammad, Mazhar, Muhammad Usama, Shah, Fawad Ali, Tipu, Muhammad Khalid
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container_title Biochemical and biophysical research communications
container_volume 729
creator Khan, Jehan Zeb
Zainab, Syeda Rida
Rehman, Mujeeb Ur
Abid, Muhammad
Mazhar, Muhammad Usama
Shah, Fawad Ali
Tipu, Muhammad Khalid
description Epilepsy is a paroxysmal abnormal hypersynchronous electrical discharge characterized by recurrent seizures. It affects more than 50 million people worldwide. Stress is the leading cause of neurodegeneration and can produce seizures that may lead to or aggravate epilepsy. Inflammation plays a vital role in epilepsy by modulating oxidative stress, and levels of neuroinflammatory cytokines including NF-κB, TNF-α, and IL-1β. Stress-induced changes in behavior were evaluated in mice by employing behavioral assessment tests such as an elevated plus maze, light-dark box, open field test, tail suspension test, Y-maze, novel object recognition test, and Morris water maze in pentylenetetrazole (PTZ) kindled mice. Behavioral changes in all these paradigms including seizure score, latency, and frequency showed an increase in symptoms in PTZ (35 mg/kg) induced seizures in stressed mice (RS-PTZ) as compared to PTZ, Stress, and normal animals. The Enzyme-linked immunosorbent assay (ELISA) results confirmed increased in serum cortisol levels. Histological examinations showed neurodegenerative changes in the hippocampus and cortex regions. The spectrophotometric evaluation showed an increase in oxidative stress by decreasing antioxidant production i.e. reduced glutathione, glutathione -s- transferase, and catalase (CAT), and increasing oxidant levels such as maloaldehyde and nitric oxide. Immunohistochemistry results showed increased expression of NF-κB, TNF-α, and IL-1β in the cortex and hippocampus of mice brains. Results from the study conclude that stress increases the likelihood of eliciting an epileptic attack by increasing the level of reactive oxygen species and neuroinflammation. •Chronic stress is an important factor in the exacerbation of epilepsy.•Chronic stress decrease seizure threshold and increases seizure susceptibility.•Neuroinflammation and oxidative stress are the main triggers to affect brain function.•NF-κB triggers the production of inflammatory cytokines e.g. TNF-α and IL-1β.
doi_str_mv 10.1016/j.bbrc.2024.150333
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It affects more than 50 million people worldwide. Stress is the leading cause of neurodegeneration and can produce seizures that may lead to or aggravate epilepsy. Inflammation plays a vital role in epilepsy by modulating oxidative stress, and levels of neuroinflammatory cytokines including NF-κB, TNF-α, and IL-1β. Stress-induced changes in behavior were evaluated in mice by employing behavioral assessment tests such as an elevated plus maze, light-dark box, open field test, tail suspension test, Y-maze, novel object recognition test, and Morris water maze in pentylenetetrazole (PTZ) kindled mice. Behavioral changes in all these paradigms including seizure score, latency, and frequency showed an increase in symptoms in PTZ (35 mg/kg) induced seizures in stressed mice (RS-PTZ) as compared to PTZ, Stress, and normal animals. The Enzyme-linked immunosorbent assay (ELISA) results confirmed increased in serum cortisol levels. Histological examinations showed neurodegenerative changes in the hippocampus and cortex regions. The spectrophotometric evaluation showed an increase in oxidative stress by decreasing antioxidant production i.e. reduced glutathione, glutathione -s- transferase, and catalase (CAT), and increasing oxidant levels such as maloaldehyde and nitric oxide. Immunohistochemistry results showed increased expression of NF-κB, TNF-α, and IL-1β in the cortex and hippocampus of mice brains. Results from the study conclude that stress increases the likelihood of eliciting an epileptic attack by increasing the level of reactive oxygen species and neuroinflammation. •Chronic stress is an important factor in the exacerbation of epilepsy.•Chronic stress decrease seizure threshold and increases seizure susceptibility.•Neuroinflammation and oxidative stress are the main triggers to affect brain function.•NF-κB triggers the production of inflammatory cytokines e.g. TNF-α and IL-1β.</description><identifier>ISSN: 0006-291X</identifier><identifier>ISSN: 1090-2104</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2024.150333</identifier><identifier>PMID: 38991397</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>blood serum ; catalase ; cortex ; cortisol ; Cytokines ; electric discharges ; elevated plus-maze test ; enzyme-linked immunosorbent assay ; epilepsy ; glutathione ; hippocampus ; immunohistochemistry ; inflammation ; neurodegenerative diseases ; Neuroinflammation ; nitric oxide ; oxidants ; Oxidative stress ; people ; PTZ-Induced seizures ; reactive oxygen species ; Restrained stress ; tail suspension test</subject><ispartof>Biochemical and biophysical research communications, 2024-10, Vol.729, p.150333, Article 150333</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. 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Histological examinations showed neurodegenerative changes in the hippocampus and cortex regions. The spectrophotometric evaluation showed an increase in oxidative stress by decreasing antioxidant production i.e. reduced glutathione, glutathione -s- transferase, and catalase (CAT), and increasing oxidant levels such as maloaldehyde and nitric oxide. Immunohistochemistry results showed increased expression of NF-κB, TNF-α, and IL-1β in the cortex and hippocampus of mice brains. 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subjects blood serum
catalase
cortex
cortisol
Cytokines
electric discharges
elevated plus-maze test
enzyme-linked immunosorbent assay
epilepsy
glutathione
hippocampus
immunohistochemistry
inflammation
neurodegenerative diseases
Neuroinflammation
nitric oxide
oxidants
Oxidative stress
people
PTZ-Induced seizures
reactive oxygen species
Restrained stress
tail suspension test
title Chronic stress intensify PTZ-induced seizures by triggering neuroinflammation and oxidative stress
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