Hydrogen inhalation exerts anti-seizure effects by preventing oxidative stress and inflammation in the hippocampus in a rat model of kainic acid-induced seizures

IF 4.4 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Neurochemistry international Pub Date : 2025-02-01 DOI:10.1016/j.neuint.2024.105925
Tzu-Kang Lin , Ming-Shang Pai , Kun-Chieh Yeh , Chi-Feng Hung , Su-Jane Wang
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Abstract

Hydrogen gas (H2) is an antioxidant with demonstrated neuroprotective efficacy. In this study, we administered H2 via inhalation to rats to evaluate its effects on seizures induced by kainic acid (KA) injection and the underlying mechanism. The animals were intraperitoneally injected with KA (15 mg/kg) to induce seizures. H2 was inhaled 2 h once a day for 5 days before KA administration. The seizure activity was evaluated using Racine's convulsion scale and electroencephalography (EEG). Neuronal cell loss, glial cell activation, and the levels of inflammatory cytokines (TNF-α, IL-1β, IL-6, CCL2, and CCL3), reactive oxygen species (ROS) and nuclear factor erythroid 2-related factor 2 (Nrf2) in the hippocampus were assessed. The cerebral blood flow of the rats was also evaluated. The results revealed that KA-treated rats presented increased seizure intensity; increased neuronal loss and astrocyte activation; increased levels of ROS, TNF-α, IL-1β, IL-6, CCL2, and CCL3; and reduced Nrf2 phosphorylation levels. Pretreatment with H2 inhalation significantly attenuated seizure intensity; prevented neuronal loss; decreased microglial and astrocytic activation; decreased ROS, TNF-α, IL-1β, IL-6, CCL2 and CCL3 levels; and increased Nrf2 levels. Inhalation of H2 also prevented the KA-induced decrease in cerebral blood flow. These results suggest that pretreatment with H2 inhalation ameliorates KA-induced seizures and inhibits the inflammatory response and oxidative stress, which protects neurons.
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在kainic酸诱导的大鼠癫痫模型中,氢吸入通过防止海马氧化应激和炎症发挥抗癫痫作用。
氢气(H2)是一种具有神经保护作用的抗氧化剂。本研究通过大鼠吸入H2,观察其对kainic acid (KA)注射液致癫痫发作的影响及其机制。腹腔注射KA (15mg /kg)诱导癫痫发作。在给药前5天,每天1次吸入H2 2 h。采用拉辛惊厥量表和脑电图(EEG)评估癫痫发作活动。评估海马神经元细胞损失、胶质细胞活化、炎症因子(TNF-α、IL-1β、IL-6、CCL2和CCL3)、活性氧(ROS)和核因子红细胞2相关因子2 (Nrf2)水平。并对大鼠的脑血流量进行了评价。结果显示,ka处理大鼠癫痫发作强度增加;神经元损失和星形胶质细胞活化增加;ROS、TNF-α、IL-1β、IL-6、CCL2、CCL3水平升高;降低Nrf2磷酸化水平。H2吸入预处理显著减弱癫痫发作强度;防止神经元丢失;小胶质细胞和星形胶质细胞活性降低;ROS、TNF-α、IL-1β、IL-6、CCL2、CCL3水平降低;Nrf2水平升高。吸入H2也能阻止ka诱导的脑血流量减少。这些结果表明,H2吸入预处理可以改善ka诱导的癫痫发作,抑制炎症反应和氧化应激,从而保护神经元。
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来源期刊
Neurochemistry international
Neurochemistry international 医学-神经科学
CiteScore
8.40
自引率
2.40%
发文量
128
审稿时长
37 days
期刊介绍: Neurochemistry International is devoted to the rapid publication of outstanding original articles and timely reviews in neurochemistry. Manuscripts on a broad range of topics will be considered, including molecular and cellular neurochemistry, neuropharmacology and genetic aspects of CNS function, neuroimmunology, metabolism as well as the neurochemistry of neurological and psychiatric disorders of the CNS.
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