The protective effect of hydroxylated fullerene pretreatment on pilocarpine-induced status epilepticus
•Hydroxylated fullerenes (HFs) has a protective effect against epileptic seizures.•HFs shows superior antioxidant capacity.•HFs shows dose-dependent antioxidant activities in epileptic rats.•Nrf2-ARE signaling pathway is involved in the neuroprotection of HFs. Status epilepticus (SE) is a neurologic...
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description | •Hydroxylated fullerenes (HFs) has a protective effect against epileptic seizures.•HFs shows superior antioxidant capacity.•HFs shows dose-dependent antioxidant activities in epileptic rats.•Nrf2-ARE signaling pathway is involved in the neuroprotection of HFs.
Status epilepticus (SE) is a neurological emergency. The pathological hallmark of neuronal damage after epileptic seizures could be the chain reaction of oxygen free radicals. Hydroxylated fullerenes (HFs) are novel and effective free radical scavengers, which play an important role in various neurological diseases. However, whether they have a protective effect against epileptic seizures remains elusive. Our study explores the effect of pretreatment with HFs in different doses (0.5, 5, and 10 mg/kg) on SEmodels induced by pilocarpine (PILO). The results suggest that HFs have a protective effect on SE in a dose-dependent manner. HFs significantly reduce the incidence of SE, prolong the latency to SE, reduce the malondialdehyde (MDA) levels, and increase the glutathione (GSH) and superoxide dismutase (SOD) levels. In addition, HFs significantly raise the expression of B-cell lymphoma-2 (Bcl-2) and reduce the expression of Bcl-2-associated X protein (Bax). We found that expressions of nuclear NF-E2-related factor 2 (nNrf2), heme oxygenase-1 (HO-1) and NADPH: quinone oxidoreductase-1 (NQO1) were upregulated 24 h after the onset of SE, but the increase was not enough to combat oxidative stress damage, nor to attenuate lipid peroxidation and apoptosis. The expressions of these proteins in HFs pretreatment groups increased more significantly than those in the epilepsy (EP) group, which effectively reduced lipid peroxidation and apoptosis in the hippocampus. In summary, these findings highlight that HFs pretreatment has a protective effect against PILO-induced SE in rats. It may relieve oxidative stress damage by activating the Nrf2-ARE signaling pathway. It provides evidence that fullerene derivatives may have therapeutic potential for epileptic seizures. |
doi_str_mv | 10.1016/j.brainres.2021.147468 |
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Status epilepticus (SE) is a neurological emergency. The pathological hallmark of neuronal damage after epileptic seizures could be the chain reaction of oxygen free radicals. Hydroxylated fullerenes (HFs) are novel and effective free radical scavengers, which play an important role in various neurological diseases. However, whether they have a protective effect against epileptic seizures remains elusive. Our study explores the effect of pretreatment with HFs in different doses (0.5, 5, and 10 mg/kg) on SEmodels induced by pilocarpine (PILO). The results suggest that HFs have a protective effect on SE in a dose-dependent manner. HFs significantly reduce the incidence of SE, prolong the latency to SE, reduce the malondialdehyde (MDA) levels, and increase the glutathione (GSH) and superoxide dismutase (SOD) levels. In addition, HFs significantly raise the expression of B-cell lymphoma-2 (Bcl-2) and reduce the expression of Bcl-2-associated X protein (Bax). We found that expressions of nuclear NF-E2-related factor 2 (nNrf2), heme oxygenase-1 (HO-1) and NADPH: quinone oxidoreductase-1 (NQO1) were upregulated 24 h after the onset of SE, but the increase was not enough to combat oxidative stress damage, nor to attenuate lipid peroxidation and apoptosis. The expressions of these proteins in HFs pretreatment groups increased more significantly than those in the epilepsy (EP) group, which effectively reduced lipid peroxidation and apoptosis in the hippocampus. In summary, these findings highlight that HFs pretreatment has a protective effect against PILO-induced SE in rats. It may relieve oxidative stress damage by activating the Nrf2-ARE signaling pathway. It provides evidence that fullerene derivatives may have therapeutic potential for epileptic seizures.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2021.147468</identifier><identifier>PMID: 33831409</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Antioxidants - metabolism ; Apoptosis - drug effects ; Dose-Response Relationship, Drug ; Fullerenes - therapeutic use ; Gene Expression Regulation - drug effects ; Glutathione - metabolism ; Hydroxylated fullerenes ; Hydroxylation ; Lipid Peroxidation - drug effects ; Male ; Neuroprotective Agents - therapeutic use ; NF-E2-Related Factor 2 - drug effects ; Nrf2-ARE signaling pathway ; Oxidative stress ; Oxidative Stress - drug effects ; Oxidative Stress - genetics ; Pilocarpine ; Rats ; Rats, Sprague-Dawley ; Status epilepticus ; Status Epilepticus - chemically induced ; Status Epilepticus - genetics ; Status Epilepticus - prevention & control ; Superoxide Dismutase-1 - biosynthesis ; Superoxide Dismutase-1 - genetics</subject><ispartof>Brain research, 2021-08, Vol.1764, p.147468-147468, Article 147468</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2021 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-c3db2806d0c25a3daaba02391d6736e2a2df7ada4b0fb72a13b399d0f559548f3</citedby><cites>FETCH-LOGICAL-c368t-c3db2806d0c25a3daaba02391d6736e2a2df7ada4b0fb72a13b399d0f559548f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006899321003255$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33831409$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cao, Huifang</creatorcontrib><creatorcontrib>Zhang, Lichao</creatorcontrib><creatorcontrib>Qu, Zhenzhen</creatorcontrib><creatorcontrib>Tian, Shuang</creatorcontrib><creatorcontrib>Wang, Zhiyong</creatorcontrib><creatorcontrib>Jiang, Yuhang</creatorcontrib><creatorcontrib>Hou, Qian</creatorcontrib><creatorcontrib>Jia, Lijing</creatorcontrib><creatorcontrib>Wang, Weiping</creatorcontrib><title>The protective effect of hydroxylated fullerene pretreatment on pilocarpine-induced status epilepticus</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>•Hydroxylated fullerenes (HFs) has a protective effect against epileptic seizures.•HFs shows superior antioxidant capacity.•HFs shows dose-dependent antioxidant activities in epileptic rats.•Nrf2-ARE signaling pathway is involved in the neuroprotection of HFs.
Status epilepticus (SE) is a neurological emergency. The pathological hallmark of neuronal damage after epileptic seizures could be the chain reaction of oxygen free radicals. Hydroxylated fullerenes (HFs) are novel and effective free radical scavengers, which play an important role in various neurological diseases. However, whether they have a protective effect against epileptic seizures remains elusive. Our study explores the effect of pretreatment with HFs in different doses (0.5, 5, and 10 mg/kg) on SEmodels induced by pilocarpine (PILO). The results suggest that HFs have a protective effect on SE in a dose-dependent manner. HFs significantly reduce the incidence of SE, prolong the latency to SE, reduce the malondialdehyde (MDA) levels, and increase the glutathione (GSH) and superoxide dismutase (SOD) levels. In addition, HFs significantly raise the expression of B-cell lymphoma-2 (Bcl-2) and reduce the expression of Bcl-2-associated X protein (Bax). We found that expressions of nuclear NF-E2-related factor 2 (nNrf2), heme oxygenase-1 (HO-1) and NADPH: quinone oxidoreductase-1 (NQO1) were upregulated 24 h after the onset of SE, but the increase was not enough to combat oxidative stress damage, nor to attenuate lipid peroxidation and apoptosis. The expressions of these proteins in HFs pretreatment groups increased more significantly than those in the epilepsy (EP) group, which effectively reduced lipid peroxidation and apoptosis in the hippocampus. In summary, these findings highlight that HFs pretreatment has a protective effect against PILO-induced SE in rats. It may relieve oxidative stress damage by activating the Nrf2-ARE signaling pathway. It provides evidence that fullerene derivatives may have therapeutic potential for epileptic seizures.</description><subject>Animals</subject><subject>Antioxidants - metabolism</subject><subject>Apoptosis - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Fullerenes - therapeutic use</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Glutathione - metabolism</subject><subject>Hydroxylated fullerenes</subject><subject>Hydroxylation</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Male</subject><subject>Neuroprotective Agents - therapeutic use</subject><subject>NF-E2-Related Factor 2 - drug effects</subject><subject>Nrf2-ARE signaling pathway</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Oxidative Stress - genetics</subject><subject>Pilocarpine</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Status epilepticus</subject><subject>Status Epilepticus - chemically induced</subject><subject>Status Epilepticus - genetics</subject><subject>Status Epilepticus - prevention & control</subject><subject>Superoxide Dismutase-1 - biosynthesis</subject><subject>Superoxide Dismutase-1 - genetics</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EoqXwC1WWbBL8SJxkB0K8pEpsytpy7LHqKi9sp6J_j6u2bNnYHvnMXM1BaElwRjDhD9uscdL2DnxGMSUZycucVxdoTqqSppzm-BLNMcY8reqazdCN99tYMlbjazRjrGIkx_UcmfUGktENAVSwO0jAmPhKBpNs9toNP_tWBtCJmdoWHPQHFoIDGTroI9Yno20HJd1oe0htrycVaR9kmHwC8Q_GYNXkb9GVka2Hu9O9QF-vL-vn93T1-fbx_LRKFeNViKduaIW5xooWkmkpG4kpq4nmJeNAJdWmlFrmDTZNSSVhDatrjU1R1EVeGbZA98e5caXvCXwQnfUK2lb2MExe0IIQyipekIjyI6rc4L0DI0ZnO-n2gmBxcCy24uxYHByLo-PYuDxlTE0H-q_tLDUCj0cA4qY7C054ZaGPZqyLcoUe7H8Zv7Qtk8E</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Cao, Huifang</creator><creator>Zhang, Lichao</creator><creator>Qu, Zhenzhen</creator><creator>Tian, Shuang</creator><creator>Wang, Zhiyong</creator><creator>Jiang, Yuhang</creator><creator>Hou, Qian</creator><creator>Jia, Lijing</creator><creator>Wang, Weiping</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20210801</creationdate><title>The protective effect of hydroxylated fullerene pretreatment on pilocarpine-induced status epilepticus</title><author>Cao, Huifang ; Zhang, Lichao ; Qu, Zhenzhen ; Tian, Shuang ; Wang, Zhiyong ; Jiang, Yuhang ; Hou, Qian ; Jia, Lijing ; Wang, Weiping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-c3db2806d0c25a3daaba02391d6736e2a2df7ada4b0fb72a13b399d0f559548f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Antioxidants - metabolism</topic><topic>Apoptosis - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Fullerenes - therapeutic use</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Glutathione - metabolism</topic><topic>Hydroxylated fullerenes</topic><topic>Hydroxylation</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Male</topic><topic>Neuroprotective Agents - therapeutic use</topic><topic>NF-E2-Related Factor 2 - drug effects</topic><topic>Nrf2-ARE signaling pathway</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Oxidative Stress - genetics</topic><topic>Pilocarpine</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Status epilepticus</topic><topic>Status Epilepticus - chemically induced</topic><topic>Status Epilepticus - genetics</topic><topic>Status Epilepticus - prevention & control</topic><topic>Superoxide Dismutase-1 - biosynthesis</topic><topic>Superoxide Dismutase-1 - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cao, Huifang</creatorcontrib><creatorcontrib>Zhang, Lichao</creatorcontrib><creatorcontrib>Qu, Zhenzhen</creatorcontrib><creatorcontrib>Tian, Shuang</creatorcontrib><creatorcontrib>Wang, Zhiyong</creatorcontrib><creatorcontrib>Jiang, Yuhang</creatorcontrib><creatorcontrib>Hou, Qian</creatorcontrib><creatorcontrib>Jia, Lijing</creatorcontrib><creatorcontrib>Wang, Weiping</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cao, Huifang</au><au>Zhang, Lichao</au><au>Qu, Zhenzhen</au><au>Tian, Shuang</au><au>Wang, Zhiyong</au><au>Jiang, Yuhang</au><au>Hou, Qian</au><au>Jia, Lijing</au><au>Wang, Weiping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The protective effect of hydroxylated fullerene pretreatment on pilocarpine-induced status epilepticus</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2021-08-01</date><risdate>2021</risdate><volume>1764</volume><spage>147468</spage><epage>147468</epage><pages>147468-147468</pages><artnum>147468</artnum><issn>0006-8993</issn><eissn>1872-6240</eissn><abstract>•Hydroxylated fullerenes (HFs) has a protective effect against epileptic seizures.•HFs shows superior antioxidant capacity.•HFs shows dose-dependent antioxidant activities in epileptic rats.•Nrf2-ARE signaling pathway is involved in the neuroprotection of HFs.
Status epilepticus (SE) is a neurological emergency. The pathological hallmark of neuronal damage after epileptic seizures could be the chain reaction of oxygen free radicals. Hydroxylated fullerenes (HFs) are novel and effective free radical scavengers, which play an important role in various neurological diseases. However, whether they have a protective effect against epileptic seizures remains elusive. Our study explores the effect of pretreatment with HFs in different doses (0.5, 5, and 10 mg/kg) on SEmodels induced by pilocarpine (PILO). The results suggest that HFs have a protective effect on SE in a dose-dependent manner. HFs significantly reduce the incidence of SE, prolong the latency to SE, reduce the malondialdehyde (MDA) levels, and increase the glutathione (GSH) and superoxide dismutase (SOD) levels. In addition, HFs significantly raise the expression of B-cell lymphoma-2 (Bcl-2) and reduce the expression of Bcl-2-associated X protein (Bax). We found that expressions of nuclear NF-E2-related factor 2 (nNrf2), heme oxygenase-1 (HO-1) and NADPH: quinone oxidoreductase-1 (NQO1) were upregulated 24 h after the onset of SE, but the increase was not enough to combat oxidative stress damage, nor to attenuate lipid peroxidation and apoptosis. The expressions of these proteins in HFs pretreatment groups increased more significantly than those in the epilepsy (EP) group, which effectively reduced lipid peroxidation and apoptosis in the hippocampus. In summary, these findings highlight that HFs pretreatment has a protective effect against PILO-induced SE in rats. It may relieve oxidative stress damage by activating the Nrf2-ARE signaling pathway. It provides evidence that fullerene derivatives may have therapeutic potential for epileptic seizures.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>33831409</pmid><doi>10.1016/j.brainres.2021.147468</doi><tpages>1</tpages></addata></record> |
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subjects | Animals Antioxidants - metabolism Apoptosis - drug effects Dose-Response Relationship, Drug Fullerenes - therapeutic use Gene Expression Regulation - drug effects Glutathione - metabolism Hydroxylated fullerenes Hydroxylation Lipid Peroxidation - drug effects Male Neuroprotective Agents - therapeutic use NF-E2-Related Factor 2 - drug effects Nrf2-ARE signaling pathway Oxidative stress Oxidative Stress - drug effects Oxidative Stress - genetics Pilocarpine Rats Rats, Sprague-Dawley Status epilepticus Status Epilepticus - chemically induced Status Epilepticus - genetics Status Epilepticus - prevention & control Superoxide Dismutase-1 - biosynthesis Superoxide Dismutase-1 - genetics |
title | The protective effect of hydroxylated fullerene pretreatment on pilocarpine-induced status epilepticus |
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