Department of Clinical Pathology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef 62511, Egypt.
Department of Animal and Poultry Management and Wealth Development, Faculty of Veterinary Medicine,Beni-Suef University, Beni-Suef 62511, Egypt.
Ecotoxicol Environ Saf. 2021 Feb;209:111820. doi: 10.1016/j.ecoenv.2020.111820. Epub 2020 Dec 29.
The objective of this study was to investigate the influence of deltamethrin (DLM)on brain function and to find whether DLM-induced neurotoxicity is prevented by the treatment with cinnamon oil. Four groups of ten Wistar albino male rats each were used. Group I (control) received saline only. Group II received cinnamon oil alone at 0.5 mg/kg B.W. intraperitonally, whereas Group III received orally DLM alone at 6 mg/kg B.W. Groups IV was treated with cinnamon oil plus DLM for 21 days to induce neurotoxicity. Rat behaviour, brain acetylcholine esterase (AChE), serotonin, oxidative stress profile were assessed. Serum sampling for the assessment of corticosterone concentration was also carried out. Finally, we demonstrate the gene expression of CYP1A1 and iNOS and the histological picture of the brain. Considering the behaviour assessment, DLM administration alone caused neurobehavioral deficits manifested by anxiety-like behavior which represented ina marked decrease in the sleeping frequency and duration, and marked increase the digging frequency and a wake non-active behavior duration. Moreover, the open field result showed a significant decrease in central square entries and duration. The neurochemical analysis revealed that DLM significantly suppressed AChE activity and elevated serotonin and corticosterone concentrations. Furthermore, results revealed thatthe brain reduced glutathione (GSH) content, superoxide dismutase (SOD) activity and malondialdehyde (MDA) concentration were significantly altered in DLM treated rats. Neurochemical disturbances were confirmed by histopathological changes in the brain. Furthermore, DLM up-regulates the mRNA expression of brain CYP1A1 and iNOS. Co-treatment with cinnamon oil exhibited significant improvement in behavioural performance and the brain antioxidant capacities with an increase in AChE activity and diminished the concentration of serotonin, serum corticosterone and MDA. Cinnamon oil treatment resulted in down-regulation of CYP1A1 and iNOS and improve the histologically picture. In conclusion, cinnamon oil ameliorated DLM-induced neurotoxicity through preventing oxidative stress-induced genotoxicity and apoptosis of brain in rats.
本研究旨在探讨氯菊酯(DLM)对大脑功能的影响,以及肉桂油是否能预防 DLM 诱导的神经毒性。使用了四组各 10 只 Wistar 白化雄性大鼠。第 I 组(对照组)仅接受生理盐水。第 II 组腹腔内给予肉桂油单独 0.5mg/kgBW,第 III 组口服给予 DLM 单独 6mg/kgBW。第 IV 组用肉桂油加 DLM 治疗 21 天诱导神经毒性。评估大鼠行为、脑乙酰胆碱酯酶(AChE)、血清素、氧化应激谱。还进行了血清采样以评估皮质酮浓度。最后,我们展示了 CYP1A1 和 iNOS 的基因表达以及大脑的组织学图片。考虑到行为评估,单独给予 DLM 会导致神经行为缺陷,表现为焦虑样行为,即睡眠频率和持续时间明显减少,挖掘频率明显增加,非活跃行为持续时间延长。此外,旷场试验结果显示中央方块进入和持续时间显著减少。神经化学分析显示 DLM 显著抑制 AChE 活性并升高血清素和皮质酮浓度。此外,结果显示 DLM 处理大鼠的大脑还原型谷胱甘肽(GSH)含量、超氧化物歧化酶(SOD)活性和丙二醛(MDA)浓度明显改变。大脑中的神经化学紊乱被证实组织学变化。此外,DLM 上调大脑 CYP1A1 和 iNOS 的 mRNA 表达。肉桂油的共同处理显著改善了行为表现和大脑抗氧化能力,增加了 AChE 活性,降低了血清素、皮质酮和 MDA 的浓度。肉桂油处理导致 CYP1A1 和 iNOS 的下调,并改善了组织学图片。总之,肉桂油通过防止氧化应激诱导的脑基因毒性和细胞凋亡,改善了 DLM 诱导的神经毒性。