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SKF83959 通过别构激活 sigma-1 受体来减轻癫痫潜伏期中的记忆损伤和抑郁样行为。

SKF83959 Attenuates Memory Impairment and Depressive-like Behavior during the Latent Period of Epilepsy via Allosteric Activation of the Sigma-1 Receptor.

机构信息

Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, 209 Tongshan Road, Xuzhou 221004, Jiangsu Province, China.

Department of Pharmacy, The Affiliated Hospital of Xuzhou Medical University, 99 West Huai-hai Road, Xuzhou 221004, Jiangsu Province, China.

出版信息

ACS Chem Neurosci. 2022 Nov 16;13(22):3198-3209. doi: 10.1021/acschemneuro.2c00629. Epub 2022 Nov 4.

DOI:10.1021/acschemneuro.2c00629
PMID:36331871
Abstract

Memory impairment and emotional disorder are two common clinical comorbidities in patients with epilepsy. It is imperative to develop a novel therapeutic agent or a strategy. 6-Chloro-7,8-dihydroxy-3-methyl-1-(3-methylphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine (SKF83959) is a dopamine-1 receptor agonist and sigma-1 receptor allosteric modulator, which displays the neuron-protective and anti-neuroinflammation activity. We examined the effect of SKF83959 on the memory impairment and emotional disorder in the latent period of epilepsy using the mice post-status epilepticus model. We found that SKF83959 ameliorated memory impairment and depressive-like mood, alleviated the neuron damage and the formation of gliosis in hippocampus, suppressed the rise of pro-inflammatory cytokines, including tumor necrosis factor-α and interleukin-1β, and induced nitric oxide synthase in the latent period of epilepsy. Additionally, SKF83959 significantly inhibited the activity of calcineurin and glycogen synthase kinase-3β. All of these protective actions were reversed by BD1047 (a sigma-1 receptor antagonist). In addition, the intra-hippocampus injection of ketoconazole (a dehydroepiandrosterone synthesis inhibitor) also reversed the protective activity of SKF83959. Thus, we concluded that SKF83959 ameliorated the memory impairment and depressive-like mood in epilepsy via allosterically activating the sigma-1 receptor and subsequently inhibiting the calcineurin/glycogen synthase kinase-3β pathway.

摘要

记忆损伤和情绪障碍是癫痫患者的两种常见临床共病。开发新型治疗药物或策略势在必行。6-氯-7,8-二羟基-3-甲基-1-(3-甲基苯基)-2,3,4,5-四氢-1H-3-苯并氮杂䓬(SKF83959)是一种多巴胺-1 受体激动剂和 sigma-1 受体变构调节剂,具有神经元保护和抗神经炎症活性。我们使用癫痫后状态的小鼠模型,研究了 SKF83959 对癫痫潜伏期记忆损伤和情绪障碍的影响。我们发现 SKF83959 改善了记忆损伤和抑郁样情绪,减轻了海马体中的神经元损伤和神经胶质形成,抑制了促炎细胞因子(包括肿瘤坏死因子-α和白细胞介素-1β)的升高,并诱导了一氧化氮合酶在癫痫潜伏期的表达。此外,SKF83959 显著抑制了钙调神经磷酸酶和糖原合成激酶-3β的活性。这些保护作用均被 BD1047(sigma-1 受体拮抗剂)逆转。此外,海马体内注射酮康唑(去氢表雄酮合成抑制剂)也逆转了 SKF83959 的保护作用。因此,我们得出结论,SKF83959 通过变构激活 sigma-1 受体,随后抑制钙调神经磷酸酶/糖原合成激酶-3β通路,改善了癫痫中的记忆损伤和抑郁样情绪。

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