Doctoral Program in Biomedical Sciences, Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia.
Department of Pharmacology and Therapeutics, Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia.
Acta Med Acad. 2023 Dec;52(3):169-181. doi: 10.5644/ama2006-124.423.
This study investigated several inflammatory markers' gene and protein expression in status epilepticus (SE) and their correlation with diazepam resistance.
Peripheral blood samples were collected from 18 adult patients with SE in Cipto Mangunkusumo Central Hospital, consisting of 12 diazepam-responsive and six diazepam-resistant samples, within 72 hours of the onset of the seizure. We collected baseline demographic and clinical data from each subject. Peripheral blood mononuclear cells (PBMCs) were isolated, cultured, stimulated with lipopolysaccharide (LPS) 1 mg/ml, and harvested for RNA isolation. The RNA was used to determine the expression of Human Mobility Group Box 1 (HMGB1), Interleukin- 6 (IL-6), IL-10, Toll-like Receptor 4 (TLR4), and Glial fibrillary acidic protein (GFAP). In addition, we performed serum protein assay of HMGB1, IL-6, IL-10, TLR4, and GFAP to compare with gene expression.
We found a significant difference between the responsive and resistant groups for serum HMGB1 and IL-6 concentration. The mRNA expression of HMGB1 and IL-6 was significantly higher in LPS-stimulated samples in the responsive but not in the resistant groups. The ratio of IL-6 to IL-10 showed a significant difference between LPS and control in the responsive group. Diazepam response was significantly correlated with seizure duration and serum protein concentration of HMGB1.
HMGB1 was highly expressed in the resistant group and strongly correlated with diazepam response, and there was a significant increase in HMGB1 mRNA expression in response to LPS stimulation. These findings suggest that targeting HMGB1 may be a promising therapeutic strategy and that HMGB1 levels could be a valuable biomarker for predicting diazepam resistance in SE.
本研究旨在探讨癫痫持续状态(SE)中几种炎症标志物的基因和蛋白表达及其与地西泮耐药的相关性。
收集了 18 例成人 SE 患者的外周血样本,其中 12 例对地西泮有反应,6 例对地西泮耐药,均在发作后 72 小时内采集。我们从每位患者收集了基线人口统计学和临床数据。分离外周血单核细胞(PBMC),培养,用 1mg/ml 的脂多糖(LPS)刺激,收获 RNA 用于分离。用 RNA 来确定人类移动组框 1(HMGB1)、白细胞介素-6(IL-6)、IL-10、Toll 样受体 4(TLR4)和胶质纤维酸性蛋白(GFAP)的表达。此外,我们还进行了血清 HMGB1、IL-6、IL-10、TLR4 和 GFAP 的蛋白测定,以与基因表达进行比较。
我们发现,在有反应组和无反应组之间,血清 HMGB1 和 IL-6 浓度有显著差异。在有反应组而非无反应组中,LPS 刺激的样本中 HMGB1 和 IL-6 的 mRNA 表达显著升高。在有反应组中,IL-6 与 IL-10 的比值在 LPS 和对照之间有显著差异。地西泮反应与癫痫持续时间和血清 HMGB1 蛋白浓度显著相关。
HMGB1 在耐药组中高表达,与地西泮反应强烈相关,LPS 刺激后 HMGB1 mRNA 表达显著增加。这些发现表明,靶向 HMGB1 可能是一种有前途的治疗策略,HMGB1 水平可能是预测 SE 中地西泮耐药的有价值的生物标志物。