Imam Aminu, Ajibola Oluwadamilola Eunice, Akorede Aalimah Akinosho, Ijomone Omamuyovwi Meashack, Ajao Moyosore Salihu
Department of Anatomy, College of Health Sciences, University of Ilorin, Ilorin, 240003, Nigeria.
Department of Biology, Illinois State University, Normal, IL, 61761, USA.
BMC Neurosci. 2025 Jul 30;26(1):48. doi: 10.1186/s12868-025-00967-3.
Epilepsy is characterized by recurrent seizures and neurological consequences, which may be associated with impaired myelin and glial integrity, and exacerbated by environmental neurotoxicants. Environmental neurotoxicants, such as Cypermethrin (CPM), may heighten these impairments, worsening seizure outcomes. This study investigates the effects of Cypermethrin (CPM) on Pentylenetetrazole (PTZ)-induced seizures and the Vitamin E (Vit E) and valproate (VAP) co-interventions on myelin and glial integrity.
Histochemical and immunohistochemical analyses for hematoxylin and eosin (H&E), myelin basic protein (MBP), ionized calcium-binding adaptor molecule 1 (IBA1), glial fibrillary acidic protein (GFAP), and oligodendrocyte transcription factor 2 (OLIG-2) were conducted on cerebral white matter and corpus callosum tissues. The density of stained cells and immunoreactivity obtained with ImageJ was subjected to one-way analysis of variance.
Immunohistochemistry revealed that cypermethrin exposure in PTZ-induced seizure rats led to marked neuronal, oligodendroglial, and myelin loss, accompanied by substantial glial activation in both cerebral white matter and corpus callosum. Interventional ingestions of VAP and Vit E, especially when combined, substantially reduced both microglial activation and reactive astrogliosis, thereby consequently preventing oligodendrocyte and neuronal loss, thus preserving both cerebral white matter and callosal myelin.
These findings highlight the potential of pyrethroid insecticides to exacerbate the neurological consequences of epilepsy, specifically causing myelin damage via glial activation. Also, the putative therapeutic synergy of antioxidant supplementation in epilepsy and neurotoxicity management was obvious.
癫痫的特征是反复发作的癫痫发作和神经学后果,这可能与髓鞘和神经胶质完整性受损有关,并会因环境神经毒物而加剧。环境神经毒物,如氯氰菊酯(CPM),可能会加剧这些损伤,使癫痫发作的后果恶化。本研究调查了氯氰菊酯(CPM)对戊四氮(PTZ)诱导的癫痫发作的影响,以及维生素E(Vit E)和丙戊酸盐(VAP)联合干预对髓鞘和神经胶质完整性的影响。
对脑白质和胼胝体组织进行苏木精和伊红(H&E)、髓鞘碱性蛋白(MBP)、离子钙结合衔接分子1(IBA1)、胶质纤维酸性蛋白(GFAP)和少突胶质细胞转录因子2(OLIG-2)的组织化学和免疫组织化学分析。使用ImageJ获得的染色细胞密度和免疫反应性进行单因素方差分析。
免疫组织化学显示,在PTZ诱导的癫痫大鼠中暴露于氯氰菊酯会导致明显的神经元、少突胶质细胞和髓鞘损失,同时脑白质和胼胝体中都有大量的神经胶质激活。VAP和Vit E的干预性摄入,特别是联合使用时,可大幅减少小胶质细胞激活和反应性星形胶质细胞增生,从而防止少突胶质细胞和神经元损失,从而保护脑白质和胼胝体髓鞘。
这些发现突出了拟除虫菊酯类杀虫剂加剧癫痫神经学后果的可能性,特别是通过神经胶质激活导致髓鞘损伤。此外,补充抗氧化剂在癫痫和神经毒性管理中的假定治疗协同作用是明显的。