Albrakati Ashraf
Department of Human Anatomy, College of Medicine, Taif University, Taif, Saudi Arabia.
Front Vet Sci. 2024 May 2;11:1361792. doi: 10.3389/fvets.2024.1361792. eCollection 2024.
Acetamiprid is a class of neuroactive insecticides widely used to control insect pests. The current study aimed to investigate the potential neuroprotective effects of luteolin against acetamiprid-induced neurotoxicity in the rat cerebral cortex. Four equal groups of adult male rats (10 in each): control, acetamiprid (40 mg/kg for 28 days), luteolin (50 mg/kg for 28 days), and acetamiprid+luteolin cotreatment were used. Acetamiprid was shown to alter the oxidative state by increasing oxidant levels [nitric oxide (NO) and malondialdehyde (MDA)] and decreasing antioxidants [glutathione (GSH), glutathione peroxidase (GPx), glutathione reductase (GR), superoxide dismutase (SOD), and catalase-(CAT)], with increased activity of nuclear factor erythroid 2-related factor 2-(Nrf2). Likewise, acetamiprid increases the inflammatory response, as evidenced by increased interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), and nuclear factor kappa B-(NF-κB). In contrast, the treatment with luteolin brought these markers back to levels close to normal, showing that it protects neurocytes from oxidative damage and the neuroinflammation effects of acetamiprid-induced inflammation. Luteolin also demonstrated a neuroprotective role via the modulation of acetylcholinesterase (AChE) activity in the cerebral cortex tissue. Histopathology showed severe neurodegenerative changes, and apoptotic cells were seen in the acetamiprid-induced cerebral cortex layer, which was evident by increased protein expression levels of Bax and caspase-3 and decreased Bcl-2 levels. Histochemistry confirmed the neuronal degeneration, as proven by the change in neurocyte colour from brown to black when stained with a silver stain. Luteolin may have a neuroprotective effect against biochemical and histopathological changes induced by acetamiprid in the rat cerebral cortex.
啶虫脒是一类广泛用于防治害虫的神经活性杀虫剂。当前研究旨在探讨木犀草素对啶虫脒诱导的大鼠大脑皮层神经毒性的潜在神经保护作用。将成年雄性大鼠分为四组,每组10只:对照组、啶虫脒组(40毫克/千克,持续28天)、木犀草素组(50毫克/千克,持续28天)以及啶虫脒与木犀草素联合治疗组。结果显示,啶虫脒通过增加氧化剂水平[一氧化氮(NO)和丙二醛(MDA)]以及降低抗氧化剂[谷胱甘肽(GSH)、谷胱甘肽过氧化物酶(GPx)、谷胱甘肽还原酶(GR)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)]来改变氧化状态,同时核因子红细胞2相关因子2(Nrf2)的活性增加。同样,啶虫脒会增加炎症反应,白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)和核因子κB(NF-κB)水平升高即为证据。相比之下,木犀草素治疗使这些指标恢复到接近正常水平,表明它能保护神经细胞免受啶虫脒诱导的氧化损伤和神经炎症影响。木犀草素还通过调节大脑皮层组织中的乙酰胆碱酯酶(AChE)活性发挥神经保护作用。组织病理学显示存在严重的神经退行性变化,在啶虫脒诱导的大脑皮层层可见凋亡细胞,这通过Bax和半胱天冬酶-3蛋白表达水平升高以及Bcl-2水平降低得以体现。组织化学证实了神经元变性,用银染色时神经细胞颜色从棕色变为黑色即可证明。木犀草素可能对啶虫脒诱导的大鼠大脑皮层生化和组织病理学变化具有神经保护作用。