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通过转录组分析在分枝珊瑚 Acropora digitifera 中发现的抗癫痫 Kunitz 样肽。

Anti-epileptic Kunitz-like peptides discovered in the branching coral Acropora digitifera through transcriptomic analysis.

机构信息

State Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Macao, China.

Department of Rehabilitation Sciences, The Hong Kong Polytechnic University, Hong Kong, China.

出版信息

Arch Toxicol. 2022 Sep;96(9):2589-2608. doi: 10.1007/s00204-022-03311-4. Epub 2022 May 23.

DOI:10.1007/s00204-022-03311-4
PMID:35604417
Abstract

Approximately 50 million people are suffering from epilepsy worldwide. Corals have been used for treating epilepsy in traditional Chinese medicine, but the mechanism of this treatment is unknown. In this study, we analyzed the transcriptome of the branching coral Acropora digitifera and obtained its Kyoto Encyclopedia of Genes and Genomes (KEGG), EuKaryotic Orthologous Groups (KOG) and Gene Ontology (GO) annotation. Combined with multiple sequence alignment and phylogenetic analysis, we discovered three polypeptides, we named them AdKuz1, AdKuz2 and AdKuz3, from A. digitifera that showed a close relationship to Kunitz-type peptides. Molecular docking and molecular dynamics simulation indicated that AdKuz1 to 3 could interact with GABA receptor but AdKuz2-GABA remained more stable than others. The biological experiments showed that AdKuz1 and AdKuz2 exhibited an anti-inflammatory effect by decreasing the aberrant level of nitric oxide (NO), IL-6, TNF-α and IL-1β induced by LPS in BV-2 cells. In addition, the pentylenetetrazol (PTZ)-induced epileptic effect on zebrafish was remarkably suppressed by AdKuz1 and AdKuz2. AdKuz2 particularly showed superior anti-epileptic effects compared to the other two peptides. Furthermore, AdKuz2 significantly decreased the expression of c-fos and npas4a, which were up-regulated by PTZ treatment. In addition, AdKuz2 reduced the synthesis of glutamate and enhanced the biosynthesis of gamma-aminobutyric acid (GABA). In conclusion, the results indicated that AdKuz2 may affect the synthesis of glutamate and GABA and enhance the activity of the GABA receptor to inhibit the symptoms of epilepsy. We believe, AdKuz2 could be a promising anti-epileptic agent and its mechanism of action should be further investigated.

摘要

全世界约有 5000 万人患有癫痫。珊瑚在传统的中医中被用于治疗癫痫,但这种治疗的机制尚不清楚。在这项研究中,我们分析了分枝珊瑚 Acropora digitifera 的转录组,获得了其京都基因与基因组百科全书(KEGG)、真核同源群(KOG)和基因本体论(GO)注释。结合多序列比对和系统发育分析,我们从 A. digitifera 中发现了三个多肽,我们将它们命名为 AdKuz1、AdKuz2 和 AdKuz3,它们与 Kunitz 型肽密切相关。分子对接和分子动力学模拟表明,AdKuz1 到 3 可以与 GABA 受体相互作用,但 AdKuz2-GABA 比其他的更稳定。生物实验表明,AdKuz1 和 AdKuz2 通过降低 LPS 诱导的 BV-2 细胞中异常水平的一氧化氮(NO)、IL-6、TNF-α 和 IL-1β,表现出抗炎作用。此外,AdKuz1 和 AdKuz2 显著抑制了戊四氮(PTZ)诱导的斑马鱼癫痫效应。AdKuz2 尤其比其他两种肽表现出更好的抗癫痫作用。此外,AdKuz2 显著降低了 c-fos 和 npas4a 的表达,c-fos 和 npas4a 是由 PTZ 处理上调的。此外,AdKuz2 减少了谷氨酸的合成,增强了γ-氨基丁酸(GABA)的生物合成。总之,这些结果表明,AdKuz2 可能通过影响谷氨酸和 GABA 的合成以及增强 GABA 受体的活性来抑制癫痫症状。我们认为,AdKuz2 可能是一种有前途的抗癫痫药物,其作用机制应进一步研究。

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