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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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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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. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c270t-86845bc60d9f871c76345437d836bb7ce21a9c5b9a7ded579104678dba727e583</cites><orcidid>0000-0002-5415-2179</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006291X24008696$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38991397$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khan, Jehan Zeb</creatorcontrib><creatorcontrib>Zainab, Syeda Rida</creatorcontrib><creatorcontrib>Rehman, Mujeeb Ur</creatorcontrib><creatorcontrib>Abid, Muhammad</creatorcontrib><creatorcontrib>Mazhar, Muhammad Usama</creatorcontrib><creatorcontrib>Shah, Fawad Ali</creatorcontrib><creatorcontrib>Tipu, Muhammad Khalid</creatorcontrib><title>Chronic stress intensify PTZ-induced seizures by triggering neuroinflammation and oxidative stress</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><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.</description><subject>blood serum</subject><subject>catalase</subject><subject>cortex</subject><subject>cortisol</subject><subject>Cytokines</subject><subject>electric discharges</subject><subject>elevated plus-maze test</subject><subject>enzyme-linked immunosorbent assay</subject><subject>epilepsy</subject><subject>glutathione</subject><subject>hippocampus</subject><subject>immunohistochemistry</subject><subject>inflammation</subject><subject>neurodegenerative diseases</subject><subject>Neuroinflammation</subject><subject>nitric oxide</subject><subject>oxidants</subject><subject>Oxidative stress</subject><subject>people</subject><subject>PTZ-Induced seizures</subject><subject>reactive oxygen species</subject><subject>Restrained stress</subject><subject>tail suspension test</subject><issn>0006-291X</issn><issn>1090-2104</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkU1r3DAQhkVpaLZp_0AORcdevBlZtmRBLmVp0kIgOaRQehH6GG-0rOVEskM3v75adttjcxKDnnlg3peQcwZLBkxcbJbWJresoW6WrAXO-RuyYKCgqhk0b8kCAERVK_bzlLzPeQPAWCPUO3LKO6UYV3JB7OohjTE4mqeEOdMQJ4w59Dt6d_-rCtHPDj3NGF7m8k_tjk4prNeYQlzTiHMaQ-y3ZhjMFMZITfR0_B18mZ7x6PxATnqzzfjx-J6RH1df71ffqpvb6--rLzeVqyVMVSe6prVOgFd9J5mTgjdtw6XvuLBWOqyZUa61ykiPvpWq3Chk562RtcS242fk88H7mManGfOkh5Adbrcm4jhnzVnLheRSwusoFL0sCbGC1gfUpTHnhL1-TGEwaacZ6H0NeqP3Neh9DfpQQ1n6dPTPdkD_b-Vv7gW4PABYAnkOmHR2AWPJOiR0k_Zj-J__D9b5mZk</recordid><startdate>20241015</startdate><enddate>20241015</enddate><creator>Khan, Jehan Zeb</creator><creator>Zainab, Syeda Rida</creator><creator>Rehman, Mujeeb Ur</creator><creator>Abid, Muhammad</creator><creator>Mazhar, Muhammad Usama</creator><creator>Shah, Fawad Ali</creator><creator>Tipu, Muhammad Khalid</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-5415-2179</orcidid></search><sort><creationdate>20241015</creationdate><title>Chronic stress intensify PTZ-induced seizures by triggering neuroinflammation and oxidative stress</title><author>Khan, Jehan Zeb ; Zainab, Syeda Rida ; Rehman, Mujeeb Ur ; Abid, Muhammad ; Mazhar, Muhammad Usama ; Shah, Fawad Ali ; Tipu, Muhammad Khalid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c270t-86845bc60d9f871c76345437d836bb7ce21a9c5b9a7ded579104678dba727e583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>blood serum</topic><topic>catalase</topic><topic>cortex</topic><topic>cortisol</topic><topic>Cytokines</topic><topic>electric discharges</topic><topic>elevated plus-maze test</topic><topic>enzyme-linked immunosorbent assay</topic><topic>epilepsy</topic><topic>glutathione</topic><topic>hippocampus</topic><topic>immunohistochemistry</topic><topic>inflammation</topic><topic>neurodegenerative diseases</topic><topic>Neuroinflammation</topic><topic>nitric oxide</topic><topic>oxidants</topic><topic>Oxidative stress</topic><topic>people</topic><topic>PTZ-Induced seizures</topic><topic>reactive oxygen species</topic><topic>Restrained stress</topic><topic>tail suspension test</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khan, Jehan Zeb</creatorcontrib><creatorcontrib>Zainab, Syeda Rida</creatorcontrib><creatorcontrib>Rehman, Mujeeb Ur</creatorcontrib><creatorcontrib>Abid, Muhammad</creatorcontrib><creatorcontrib>Mazhar, Muhammad Usama</creatorcontrib><creatorcontrib>Shah, Fawad Ali</creatorcontrib><creatorcontrib>Tipu, Muhammad Khalid</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khan, Jehan Zeb</au><au>Zainab, Syeda Rida</au><au>Rehman, Mujeeb Ur</au><au>Abid, Muhammad</au><au>Mazhar, Muhammad Usama</au><au>Shah, Fawad Ali</au><au>Tipu, Muhammad Khalid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronic stress intensify PTZ-induced seizures by triggering neuroinflammation and oxidative stress</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2024-10-15</date><risdate>2024</risdate><volume>729</volume><spage>150333</spage><pages>150333-</pages><artnum>150333</artnum><issn>0006-291X</issn><issn>1090-2104</issn><eissn>1090-2104</eissn><abstract>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.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38991397</pmid><doi>10.1016/j.bbrc.2024.150333</doi><orcidid>https://orcid.org/0000-0002-5415-2179</orcidid></addata></record> |
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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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