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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Veröffentlicht in:Brain research 2021-08, Vol.1764, p.147468-147468, Article 147468
Hauptverfasser: Cao, Huifang, Zhang, Lichao, Qu, Zhenzhen, Tian, Shuang, Wang, Zhiyong, Jiang, Yuhang, Hou, Qian, Jia, Lijing, Wang, Weiping
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container_title Brain research
container_volume 1764
creator Cao, Huifang
Zhang, Lichao
Qu, Zhenzhen
Tian, Shuang
Wang, Zhiyong
Jiang, Yuhang
Hou, Qian
Jia, Lijing
Wang, Weiping
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.
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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. 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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><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 &amp; 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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.</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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