A Hosny Sara, M Abdelmenem Alshaymaa, Azouz Taha, S Kamar Samaa, M ShamsEldeen Asmaa, A El-Shafei Asmaa
Histology Department, Faculty of Medicine, Cairo University, Manial, Cairo, Egypt.
Histology Department, Faculty of Medicine, Fayoum University, Egypt.
Acta Histochem Cytochem. 2023 Oct 31;56(5):77-86. doi: 10.1267/ahc.23-00027. Epub 2023 Oct 4.
Autism is a neurodevelopmental disorder that impairs communication and social interaction. This study investigated the possible beneficial effects of erythropoietin (EPO) on experimental autistic-like behaviors induced by propionic acid (PPA). Twenty-four rats were distributed into three groups: (i) control; (ii) PPA_Gp: daily injected subcutaneously with PPA for five consecutive days; PPA+EPO-Gp: injected with PPA, then received intraperitoneal injection of EPO once daily for two weeks. Behavioral changes in the rats were assessed. Specimens from the cerebellar hemispheres were subjected to histological and ultrastructure examination, immunohistochemistry for glial fibrillary acidic protein (GFAP) and calbindin-D28K, and biochemical analysis for glutathione peroxidase (GSH-Px), malondialdehyde (MDA), gamma amino-butyric acid (GABA), and serotonin. PPA-Gp showed significant behavioral impairment, with a significant depletion in GSH-px, GABA, and serotonin and a significant increase in MDA. Histological examination revealed reduced Purkinje cell count with ultrastructural degeneration, irregularly arranged nerve fibers in the molecular layer, astrogliosis, and significantly decreased calbindin-immunostaining compared to the control. EPO protected cerebellar structure, increased Purkinje cell count, improved neuronal morphology, reduced PPA-induced autistic-like features, alleviated neuronal oxidative stress, increased intercellular antioxidant levels, and suppressed inflammation. EPO provided significant protection against PPA-induced autistic features in rats, with structural preservation of Purkinje cells.
自闭症是一种损害沟通和社交互动的神经发育障碍。本研究调查了促红细胞生成素(EPO)对丙酸(PPA)诱导的实验性自闭症样行为可能产生的有益影响。将24只大鼠分为三组:(i)对照组;(ii)PPA组:连续五天每天皮下注射PPA;PPA+EPO组:注射PPA后,每天腹腔注射一次EPO,持续两周。评估大鼠的行为变化。对小脑半球的标本进行组织学和超微结构检查、胶质纤维酸性蛋白(GFAP)和钙结合蛋白-D28K的免疫组织化学检查,以及谷胱甘肽过氧化物酶(GSH-Px)、丙二醛(MDA)、γ-氨基丁酸(GABA)和血清素的生化分析。PPA组表现出明显的行为损害,GSH-px、GABA和血清素显著减少,MDA显著增加。组织学检查显示,与对照组相比,浦肯野细胞数量减少,超微结构退化,分子层神经纤维排列不规则,星形胶质细胞增生,钙结合蛋白免疫染色显著降低。EPO保护小脑结构,增加浦肯野细胞数量,改善神经元形态,减少PPA诱导的自闭症样特征,减轻神经元氧化应激,提高细胞间抗氧化水平,并抑制炎症。EPO对大鼠PPA诱导的自闭症特征提供了显著保护,浦肯野细胞结构得以保留。