Costet-Mejía Alejandro, Trejo-Tapia Gabriela, Baca-Ibarra Itzel Isaura, Rodríguez-Hernández Aida Araceli, García-Hernández Julio, Camacho-Díaz Brenda Hildeliza, Zamilpa Alejandro
Centro de Desarrollo de Productos Bióticos (CEPROBI), Instituto Politécnico Nacional, Yautepec 62739, Morelos, Mexico.
Centro de Investigación Biomédica del Sur (CIBIS), Instituto Mexicano del Seguro Social (IMSS), Xochitepec 62780, Morelos, Mexico.
Pharmaceuticals (Basel). 2024 Sep 9;17(9):1184. doi: 10.3390/ph17091184.
L'Her Ex. Aiton, presenting antioxidant and anti-inflammatory activities, is traditionally used to treat bruises and headaches and as a healing agent. This study aimed to investigate whether its organic fraction (EAOr) has neuroprotective properties against neuroinflammation in the context of ischemia/reperfusion.
The chemical composition of EAOr was determined using HPLC techniques, and its neuroprotective activities were evaluated in a common carotid-artery ligation model for the induction of ischemia/reperfusion (I/R). The animals were supplemented with EAOR for 15 days. On the last day, the animals were rested for one hour, following which the common carotid-artery ligation procedure was performed to induce I/R. The neurological deficit was evaluated at 24 h after I/R using Bederson's scale, and the relative expression of inflammatory genes and structure of hippocampal neurons were analyzed at 48 h.
The chemical analysis revealed five major compounds in EAOr: gallic acid, rutin, ellagic acid, and glucoside and rhamnoside quercetin. EAOr prevented neurological deficit 24 h after I/R; led to the early activation of the and genes; reduced , , and gene expression; and protected hippocampal neurons.
Our findings demonstrate that EAOr contains polyphenol-type compounds, which could exert a therapeutic effect through the inhibition of neuroinflammation and neuronal death genes, thus maintaining hippocampal neurons.
艾顿草具有抗氧化和抗炎活性,传统上用于治疗瘀伤和头痛,并作为一种愈合剂。本研究旨在探讨其有机组分(EAOr)在缺血/再灌注情况下对神经炎症是否具有神经保护特性。
采用高效液相色谱技术测定EAOr的化学成分,并在颈总动脉结扎模型中评估其对缺血/再灌注(I/R)诱导的神经保护活性。给动物补充EAOR 15天。在最后一天,让动物休息1小时,然后进行颈总动脉结扎手术以诱导I/R。在I/R后24小时使用贝德森量表评估神经功能缺损,并在48小时分析炎症基因的相对表达和海马神经元的结构。
化学分析显示EAOr中有五种主要化合物:没食子酸、芦丁、鞣花酸、糖苷和鼠李糖苷槲皮素。EAOr可预防I/R后24小时的神经功能缺损;导致和基因的早期激活;降低、、和基因表达;并保护海马神经元。
我们的研究结果表明,EAOr含有多酚类化合物,可通过抑制神经炎症和神经元死亡基因发挥治疗作用,从而维持海马神经元。