RESUMEN
Disruption of gamma-amino butyric acid type A receptors (GABAA Rs) synaptic clustering and a decrease in the number of GABAA Rs in the plasma membrane are thought to contribute to alteration of the balance between excitatory and inhibitory neurotransmission, which promotes seizure induction and propagation. The multipass transmembrane protein cleft lip and palate transmembrane protein 1 (Clptm1) controls the forward trafficking of GABAA R, thus decaying miniature inhibitory postsynaptic current (mIPSC) of inhibitory synapses. In this study, using a pentylenetetrazol (PTZ)-induced epilepsy rat model, we found that Clptm1 regulates epileptic seizures by modulating GABAA R-mediated inhibitory synaptic transmission. First, we showed that Clptm1 expression was elevated in the PTZ-induced epileptic rats. Subsequently, we found that downregulation of Clptm1 expression protected against PTZ-induced seizures, which was attributed to an increase in the number of GABAA Rγ2s in the plasma membrane and the amplitude of mIPSC. Taken together, our findings identify a new anti-seizure target that provides a theoretical basis for the development of novel strategies for the prevention and treatment of epilepsy.
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Labio Leporino , Fisura del Paladar , Epilepsia , Animales , Ratas , Epilepsia/inducido químicamente , Epilepsia/genética , Ácido gamma-Aminobutírico , Proteínas de la Membrana/metabolismo , Pentilenotetrazol/toxicidad , Receptores de GABA-A/genética , Receptores de GABA-A/metabolismo , Convulsiones/inducido químicamente , Convulsiones/genética , Transmisión Sináptica/genéticaRESUMEN
Multiple approaches are used to treat acne scars, but some are expensive, ineffective, and cause complications. We aimed to evaluate the efficacy and safety of ultra-pulsed CO2 fractional laser combined with 30% supramolecular salicylic acid in the treatment of acne scars in a prospective split-face control study. Twenty patients with facial symmetrical acne scars were enrolled. One side of face was randomly treated with 30% supramolecular salicylic acid, and two sides were treated with ultra-pulsed CO2 fractional laser. The Echelle d'evaluation clinique des cicatrices d'acne (ECCA) scale was used to evaluate the clinical efficacy before and 3 months after treatment, and a quartile scale was used to self-evaluate the improvement of patients. A visual analog scale was used to record pain scores after each treatment, and side effects and other adverse reactions on the face were recorded. All the patients completed treatment and follow-up. There was statistical difference in ECCA scores of bilateral facial acne scars after three treatments (p < 0.001). ECCA scores on the combined side were lower after three treatments than those on the laser side (p = 0.003). The patient satisfaction quartile scale on the combined side was higher than that on the laser side alone (p = 0.015). Ultra-pulsed CO2 fractional laser combined with 30% supramolecular salicylic acid has better efficacy in the treatment of acne scars than laser alone, and patient self-assessment of combined treatment has a greater degree of improvement in acne scars, and does not increase patient pain scores and related adverse reactions.
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Acné Vulgar , Láseres de Gas , Acné Vulgar/complicaciones , Dióxido de Carbono , Cicatriz/diagnóstico , Cicatriz/etiología , Cicatriz/terapia , Humanos , Láseres de Gas/efectos adversos , Dolor/etiología , Estudios Prospectivos , Ácido Salicílico/efectos adversos , Resultado del TratamientoRESUMEN
Secreted frizzled-related protein 5 (SFRP5) plays a pivotal role in regulating the development of many tissues and organs, however, as an inhibitor of Wnt signaling, the role of SFRP5 in vitiligo remains unknown. Hence, we speculated that SFRP5 might be associated with melanogenesis in melanocytes by regulating Wnt signaling in vitiligo. In this study, we found that SFRP5 was overexpressed in the skin lesions of patients with vitiligo. Compared with that in normal epidermal melanocytes (PIG1), the expression of SFRP5 was increased in vitiligo melanocytes (PIG3V). To investigate the effect of SFRP5 on melanin synthesis, PIG1 cells were infected with recombinant SFRP5 adenovirus (AdSFRP5), and PIG3V cells were infected with recombinant siSFRP5 adenovirus (AdsiSFRP5). The results showed that SFRP5 overexpression inhibited melanin synthesis in PIG1 cells through downregulation of microphthalmia-associated transcription factor (MITF) and its target proteins via suppression of the Wnt/ß-catenin signaling pathway. Accordingly, SFRP5 silencing increased melanin synthesis and activated the Wnt signaling pathway in PIG3V cells. Moreover, SFRP5 overexpression also downregulated the transcriptional activity of T cell factor/lymphoid enhancer factor (TCF/LEF) in PIG1 cells. Furthermore, this inhibitory effect of SFRP5 on melanin synthesis was reversed by treatment with the ß-catenin agonist, SKL2001. The inhibitory action of SFRP5 in pigmentation was further confirmed in vivo using a nude mouse model. Hence, our results indicate that SFRP5 can inhibit melanogenesis in melanocytes. Additionally, our findings showed that SFRP5 plays a vital role in the development of vitiligo, and thus may serve as a potential therapeutic target for vitiligo.
RESUMEN
Lim kinase1 (LIMK1) plays a vital role in dendritic spine morphogenesis and brain function. However, the mechanism of LIMK1 in epilepsy remains unclear. Our study showed that LIMK1 was upregulated in the hippocampal dentate gyrus (DG) of a pentylenetetrazol (PTZ)-kindled epilepsy rat model. Downregulation of LIMK1 reduced susceptibility to seizures in the PTZ-induced rat model, whereas combined LIMK1 knockdown and jasplakinolide treatment increased the duration of stage 4-5 seizures in PTZ-kindled rats. Via in vitro experiments, we explored the possible mechanism of LIMK1 in seizures. LIMK1 was closely related to actin depolymerization and dendritic spine maturation in Mg2+-free treated hippocampal neurons. Additionally, LIMK1 affected actin polymerization by regulating the level of p-cofilin. Mechanistically, our results show that LIMK1 regulates actin-mediated alterations in dendritic spine morphology in epileptic rats, which requires cofilin phosphorylation. Taken together, our results show that LIMK1 is involved in the spatial control of actin dynamics and kinase signaling in seizures, providing new insights into structural plasticity mechanisms in epilepsy.
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Factores Despolimerizantes de la Actina/metabolismo , Actinas/metabolismo , Quinasas Lim/metabolismo , Convulsiones/metabolismo , Convulsiones/fisiopatología , Animales , Hipocampo/metabolismo , Masculino , Neuronas/metabolismo , Fosforilación , Proteínas Quinasas/metabolismo , Ratas Sprague-DawleyRESUMEN
AIMS: Semaphorin7A (Sema7A) plays an important role in the immunoregulation of the brain. In our study, we aimed to investigate the expression patterns of Sema7A in epilepsy and further explore the roles of Sema7A in the regulation of seizure activity and the inflammatory response in PTZ-kindled epileptic rats. METHODS: First, we measured the Sema7A expression levels in patients with temporal lobe epilepsy (TLE) and in rats of a PTZ-kindled epilepsy rat model. Second, to explore the role of Sema7A in the regulation of seizure activity, we conducted epilepsy-related behavioral experiments after knockdown and overexpression of Sema7A in the rat hippocampal dentate gyrus (DG). Possible Sema7A-related brain immune regulators (eg, ERK phosphorylation, IL-6, and TNF-α) were also investigated. Additionally, the growth of mossy fibers was visualized by anterograde tracing using injections of biotinylated dextran amine (BDA) into the DG region. RESULTS: Sema7A expression was markedly upregulated in the brain tissues of TLE patients and rats of the epileptic model after PTZ kindling. After knockdown of Sema7A, seizure activity was suppressed based on the latency to the first epileptic seizure, number of seizures, and duration of seizures. Conversely, overexpression of Sema7A promoted seizures. Overexpression of Sema7A increased the expression levels of the inflammatory cytokines, IL-6 and TNF-α, ERK phosphorylation, and growth of mossy fibers in PTZ-kindled epileptic rats. CONCLUSION: Sema7A is upregulated in the epileptic brain and plays a potential role in the regulation of seizure activity in PTZ-kindled epileptic rats, which may be related to neuroinflammation. Sema7A promotes the inflammatory cytokines TNF-α and IL-6 as well as the growth of mossy fibers through the ERK pathway, suggesting that Sema7A may promote seizures by increasing neuroinflammation and activating pathological neural circuits. Sema7A plays a critical role in epilepsy and could be a potential therapeutic target for this neurological disorder.
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Antígenos CD/genética , Convulsivantes , Pentilenotetrazol , Convulsiones/genética , Semaforinas/genética , Adolescente , Adulto , Animales , Niño , Preescolar , Giro Dentado/metabolismo , Epilepsia del Lóbulo Temporal/genética , Epilepsia del Lóbulo Temporal/fisiopatología , Femenino , Proteínas Ligadas a GPI/genética , Técnicas de Silenciamiento del Gen , Humanos , Interleucina-6/genética , Excitación Neurológica , Sistema de Señalización de MAP Quinasas , Masculino , Fibras Musgosas del Hipocampo/patología , Ratas , Ratas Sprague-Dawley , Convulsiones/inducido químicamente , Convulsiones/psicología , Factor de Necrosis Tumoral alfa/genética , Regulación hacia Arriba , Adulto JovenRESUMEN
Purinergic P2X3 receptors (P2X3Rs) play extensive roles in nerve cells in the central nervous system, particularly in hyperexcitability and calcium (Ca(2+)) influx. However, the role of P2X3Rs in epilepsy has not been previously investigated. To determine the relationship between P2X3Rs and epilepsy, the expression and cellular location of P2X3Rs in patients with intractable temporal lobe epilepsy (TLE) and in a lithium chloride-pilocarpine-induced chronic rat model of epilepsy were assessed. Furthermore, the function of P2X3Rs was assessed in vitro. Real-time quantitative polymerase chain reaction (RT-qPCR) and Western blot analysis were used to evaluate the expression levels of P2X3Rs in brain tissues from TLE patients and an epileptic rat model, whereas immunofluorescence labeling was applied to determine the distribution of target proteins. Whole-cell recording was subsequently performed to identify the influence of P2X3Rs on seizure-like discharges. P2X3Rs were located at the cell bodies and dendrites of neurons with significantly increased expression in the TLE patients and epileptic rat model. In vitro, P2X3R activation accelerated sustained repetitive firing, whereas P2X3R inhibition led to relatively low-frequency discharges. To the best of our knowledge, this is the first study provide evidence that upregulated P2X3R expression exists in both epileptic humans and rats and may aggravate the epileptic state in vitro. Thus, P2X3Rs may represent a novel therapeutic target for antiepileptic drugs.
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Modelos Animales de Enfermedad , Epilepsia del Lóbulo Temporal/metabolismo , Receptores Purinérgicos P2X3/biosíntesis , Regulación hacia Arriba/fisiología , Potenciales de Acción/fisiología , Adolescente , Adulto , Animales , Epilepsia del Lóbulo Temporal/inducido químicamente , Epilepsia del Lóbulo Temporal/fisiopatología , Femenino , Regulación de la Expresión Génica , Humanos , Masculino , Persona de Mediana Edad , Pilocarpina/toxicidad , Ratas , Ratas Sprague-Dawley , Adulto JovenRESUMEN
OBJECTIVE: Drosophila Pumilio (Pum), a homolog of mammalian Pum2, plays an important role in translational regulation in the central nervous system (CNS), particularly for dendrite outgrowth and neuronal excitability. We investigated the expression pattern and cellular distribution of Pum2 in patients with drug-refractory temporal lobe epilepsy (TLE) and rats with lithium chloride-pilocarpine-induced epilepsy. METHODS: Real-time quantitative PCR (RT-qPCR), Western blot, immunohistochemistry, and double-labeled immunofluorescence were utilized to determine the expression level and distribution of Pum2 in temporal neocortex tissues from patients with intractable TLE (n=20) and patients with severe head trauma (n=20) in addition to the hippocampus and adjacent cortex of rats with lithium chloride-pilocarpine-induced TLE and controls. RESULTS: Pum2 was expressed in the cell bodies and dendrites of neurons but did not colocalize with glial fibrillary acidic protein-positive astrocytes or propidium iodide (PI) in nuclei. The expression of Pum2 was significantly reduced in patients and rats with TLE in comparison to controls (P<0.05). CONCLUSION: Pum2 expression was less in patients with TLE and a rodent model of epilepsy, suggesting that decreased expression of Pum2 may be involved in the pathogenesis of TLE.
Asunto(s)
Epilepsia del Lóbulo Temporal/patología , Proteínas de Unión al ARN/metabolismo , Lóbulo Temporal/metabolismo , Adolescente , Adulto , Animales , Astrocitos/metabolismo , Western Blotting , Estudios de Casos y Controles , Dendritas/metabolismo , Modelos Animales de Enfermedad , Epilepsia del Lóbulo Temporal/metabolismo , Femenino , Hipocampo/metabolismo , Humanos , Inmunohistoquímica , Masculino , Neocórtex/metabolismo , Neuronas/metabolismo , Reacción en Cadena de la Polimerasa/métodos , Ratas , Ratas Sprague-Dawley , Lóbulo Temporal/patología , Adulto JovenRESUMEN
This study was aimed to examine whether the Na(+)/K(+) adenosine triphosphatase (Na(+)/K(+)-ATPase) activity in ischemic penumbra is associated with the pathogenesis of ischemia/reperfusion-induced brain injury. An experimental model of cerebral ischemia/reperfusion was made by transient middle cerebral artery occlusion (tMCAO) in rats and the changes of Na(+)/K(+)-ATPase activity in the ischemic penumbra was examined by Enzyme Assay Kit. Extensive infarction was observed in the frontal and parietal cortical and subcortical areas at 6 h, 24 h, 48 h, 3 d and 7 d after tMCAO. Enzyme Assay analyses revealed the activity of Na(+)/K(+)-ATPase was decreased in the ischemic penumbra of model rats after focal cerebral ischemia/reperfusion compared with sham-operated rats, and reduced to its minimum at 48 h, while the infarct volume was enlarged gradually. In addition, accompanied by increased brain water content, apoptosis-related bcl-2 and Bax proteins, apoptotic index and neurologic deficits Longa scores, but fluctuated the ratio of bcl-2/Bax. Correlation analysis showed that the infarct volume, apoptotic index, neurologic deficits Longa scores and brain water content were negatively related with Na(+)/K(+)-ATPase activity, while the ratio of bcl-2/Bax was positively related with Na(+)/K(+)-ATPase activity. Our results suggest that down-regulated Na(+)/K(+)-ATPase activity in ischemic penumbra might be involved in the pathogenesis of cerebral ischemia/reperfusion injury presumably through the imbalance ratio of bcl-2/Bax and neuronal apoptosis, and identify novel target for neuroprotective therapeutic intervention in cerebral ischemic disease.
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Isquemia Encefálica/enzimología , Isquemia Encefálica/patología , Daño por Reperfusión/enzimología , Daño por Reperfusión/patología , ATPasa Intercambiadora de Sodio-Potasio/metabolismo , Animales , Apoptosis/fisiología , Modelos Animales de Enfermedad , Regulación hacia Abajo , Inmunohistoquímica , Etiquetado Corte-Fin in Situ , Masculino , Ratas , Ratas Sprague-DawleyRESUMEN
This research described the heterogeneous reactions of persulfate with different particle sizes of zero-valent iron (including 1 mm-ZVI,150 µm-ZVI,50 nm-ZVI) for degradation of acid orange 7(AO7) , and studied the kinetics and intermediate products of AO7 under these systems. The results demonstrated that these three types of ZVI were efficient in promoting the degradation of AO7, the degradation efficiencies of AO7 were 43% , 97% , and 100% within 90 min respectively, in the 1 mm-ZVI,150 µm-ZVI and 50 nm- ZVI systems, respectively. With the results of kinetic fitting models, the pseudo first-order kinetics exhibited better fitting results in the 1 mm-ZVI,150 µm-ZVI systems, while the second-order kinetics exhibited better fitting results in the 50 nm-ZVI system. And the different ZVI types exhibited difference on the AO7 degradation rate constant, which ranged as 50 nm-ZVI > 150 µm-ZVI > 1 mm-ZVI. The iron corrosion products coating on the ZVI after reaction were composed of α-Fe2 O3 and some Fe3O4 in the 1 mm-ZVI system while that consisted of Fe3O4 and α-Fe2O3, FeOOH respectively, in thel50 µm-ZVI and 50 nm-ZVI systems,. Which were identified by scanning electron microscope (SEM) with energy dispersive spectrometer (EDS) and Raman spectroscopy. Some intermediate products, including 2-naphthalenol, 2-methylphenol, 4-ethyl- 3-methyl-phenol, isoindole- 1,3-dione and phthalic acid et al. were identified by GC/MS measurement. Both UV-vis absorbance spectra and GC/MS determination indicated that there was difference in degradation paths of AO7 between the three systems.
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Compuestos Azo/química , Bencenosulfonatos/química , Hierro/química , Tamaño de la Partícula , Sulfatos/química , Cinética , Modelos TeóricosRESUMEN
Extracellular signal-regulated protein kinase, ERK1/2 is activated by phosphorylation (p-ERK1/2) during environmental stress such as epileptiform discharge. We investigated the role of ERK1/2 in abnormal axon growth and synapse reorganization in cultured neurons displaying epileptiform activity. The cultured neurons displaying epileptiform activity were treated with magnesium-free extracellular fluid for 3h and monitored epileptiform discharges using whole-cell patch clamp. Two study groups, neurons displaying epileptiform activity and the same neurons treated with ERK1/2 inhibitor U0126, were studied at six time points, 0 min, 30 min, 2h, 6h, 12h, and 24h following discharge. The expressions of p-ERK1/2, C-fos, growth-associated protein 43 (GAP-43) and synaptophysin (SYP), as markers of axon growth and synapse reorganization, were investigated by double-label immunofluorescence and western blotting. In the neurons displaying epileptiform activity, p-ERK1/2 was detected immediately following discharge, and expression peaked at 30 min. The expression of C-fos, GAP-43 and SYP followed the same pattern as p-ERK1/2. In the treated group, p-ERK1/2 was inhibited completely, and C-fos, GAP-43 and SYP were reduced. These findings indicate that epileptiform discharge activates ERK1/2 which regulates C-fos in cultured neurons displaying epileptiform activity, and this cascade may upregulate GAP-43 and SYP to contribute to axon growth and synapse reorganization to potentiate epileptic activities.
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Quinasas MAP Reguladas por Señal Extracelular/metabolismo , Proteína GAP-43/metabolismo , Hipocampo/citología , Neuronas/efectos de los fármacos , Sinaptofisina/metabolismo , Regulación hacia Arriba/fisiología , Potenciales de Acción/efectos de los fármacos , Potenciales de Acción/fisiología , Animales , Animales Recién Nacidos , Células Cultivadas , Inhibidores Enzimáticos/farmacología , Magnesio/metabolismo , Ratas , Ratas Wistar , Factores de Tiempo , Regulación hacia Arriba/efectos de los fármacosRESUMEN
OBJECTIVE: To investigate the activation pattern of extracellular signal-regulated kinase 1/2 (ERK1/2) in the hippocampus of mice during pilocarpine-induced status epilepticus (SE) and its relationship with reactive astrogliosis. METHODS: Status epilepticus (SE) models were established by intraperitoneal injection of pilocarpine. The intervention group received the ERK1/2 signaling pathway inhibitor SL327 before the pilocarpine injection. We evaluated the SE model group, the intervention group and the control saline-treated group, at 6 hours and 3 days after initiation of the seizure. Phosphorylated activated ERK1/2 and glial fibrillary acidic protein (GFAP) were labeled with both single-labeling and sequential single-labeling immunohistochemical techniques. RESULTS: Among the pilocarpine-treated (SE model) mice, strong immunohistochemical staining of phospho-ERK1/2 was observed in the neurons and astrocytes of the hippocampus at 6 hours after initiation of SE, whereas staining on the third day of SE was not different from the control saline-treated mice. In the SL327-treated mice (intervention group), SL327 effectively blocked the ERK1/2 activation and little gliosis could be detected at 6 hours and 3 days after initiation of SE; the levels of phospho-ERK1/2 remained low, but the level of gliosis was similar to that of SE mice. CONCLUSION: The ERK1/2 signaling pathway plays an important role in the early stage of reactive astrogliosis in mice with pilocarpine-induced SE.
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Astrocitos/metabolismo , Gliosis/metabolismo , Proteína Quinasa 3 Activada por Mitógenos/metabolismo , Pilocarpina/farmacología , Estado Epiléptico/metabolismo , Animales , Astrocitos/efectos de los fármacos , Astrocitos/patología , Recuento de Células , Proteína Ácida Fibrilar de la Glía/metabolismo , Gliosis/patología , Hipocampo/efectos de los fármacos , Hipocampo/metabolismo , Hipocampo/patología , Inmunohistoquímica , Masculino , Ratones , Fosforilación , Distribución Aleatoria , Transducción de Señal/fisiología , Estado Epiléptico/inducido químicamente , Estado Epiléptico/patología , Factores de TiempoRESUMEN
Epithelial membrane protein-1 (EMP-1), called Tumor-associated membrane protein, is the marker of a drug-resistant tumor and take part in the drug-resistant mechanism of tumor, with the relationship of epidermal growth factor receptor (EGFR). Because there are some similarities between the pathogenesis and the drug resistance mechanism of tumor and the drug resistance mechanisms in epilepsy. EMP1 expression may be connected with the drug-resistance mechanism of epilepsy. We detected EMP-1 by gene scanning and immunohistochemistry staining, comparing the IE group and the control group, and we investigated the relationship between EMP-1 and EGFR by double-label immunofluorescence staining in the IE group. We found expression of EMP-1 mRNA was higher in IE per the gene scanning, EMP-1 immunoreactivity was apparent in neurons of IE patients but not in the control group, and the expression of EMP-1 and EGFR occurred in the same neuron. We confirm EMP-1 is abnormally expressed in IE and suggest the interaction of EGFR and EMP-1 plays a role in the mechanism of drug resistance in epilepsy and may be a new gene for drug resistance.
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Epilepsia/metabolismo , Receptores ErbB/biosíntesis , Neocórtex/metabolismo , Proteínas de Neoplasias/biosíntesis , Receptores de Superficie Celular/biosíntesis , Adolescente , Adulto , Anticonvulsivantes/uso terapéutico , Niño , Resistencia a Medicamentos , Epilepsia/tratamiento farmacológico , Receptores ErbB/metabolismo , Femenino , Humanos , Masculino , Persona de Mediana Edad , Regulación hacia ArribaRESUMEN
We aimed to develop a double-injection model of intracerebral hemorrhage (ICH) in rabbits and to evaluate it as a tool for investigating post-ICH brain injury. Rabbits were injected with 300microL fresh autologous whole blood into the right basal ganglia. Behavioral changes were rated, brain water content (BWC) was measured and brain tissue morphology was also examined. ICH was established in 93.5% of the blood injection group. At 1, 3 and 7 days after ICH, there were significant differences in the total neurological scores (p<0.01) and BWC (p<0.01) between a sham-operated group and the ICH group. These findings suggest that the model produces a persistent neurological deficit, hematoma volume and perihematomal edema and closely mimics human hypertensive basal ganglia ICH; it is a controllable and reproducible hematoma that lends itself to quantitative investigation.
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Hemorragia Cerebral , Modelos Animales de Enfermedad , Animales , Hemorragia de los Ganglios Basales/patología , Hemorragia de los Ganglios Basales/fisiopatología , Conducta Animal , Coagulación Sanguínea/fisiología , Edema Encefálico/etiología , Hemorragia Cerebral/complicaciones , Hemorragia Cerebral/etiología , Hemorragia Cerebral/patología , Estado de Conciencia/fisiología , Inyecciones , Masculino , Actividad Motora/fisiología , Enfermedades del Sistema Nervioso/etiología , Conejos , Factores de TiempoRESUMEN
OBJECTIVE: To investigate the correlation between ERK1/2 cascade and c-fos after hippocampal neuron epileptiform discharge. METHODS: Hippocampal neurons were collected from Wistar rats and cultured in magnesium-free extra-cellular fluid to establish hippocampal neuron epileptiform discharge model. Then the hippocampal neurons were divided into 2 groups: inhibitor group, added with 10 micromol/L U0126, inhibitor of ERK 1/2 pathway, and control group without any treatment, got at 0 min). Using double-label immunofluorescence, laser scanning confocal microscopy was performed to detect the disposition of phosphorylated-ERK1/2(p-ERK1/2) and c-fos in the neurons. Western blotting was used to detect the expression of p-ERK1/2 and c-fos 0 min, 30 min, 2 h, 6 h, 12 h, and 24 h following corresponding treatment RESULTS: Double-label immunofluorescence examination displayed that there was p-ERK1/2 in both the cytoplasm and nucleus, but c-fos in the nucleus only. Western blotting manifested that p-ERK1/2 was observed at each time points in the model group, and the expression pattern of c-fos was the same as p-ERK1/2, which peaked 30 min after treatment. In the inhibitor group, p-ERK1/2 was inhibited completely, and c-fos was decreased obviously. The c-fos expression levels at different time points of the inhibitor group were all significantly lower than those of the model group (all P < 0.01). CONCLUSION: After hippocampal neuron epileptiform discharge, ERK1/2 is activated for a long time, and the expression of c-fos is downregulated by blocking the phosphorylation of ERK1/2.