Cadi Ayyad University, Faculty of Sciences Semlalia, Neurosciences, Pharmacology and Environment Unit, Avenue My Abdellah, B.P. 2390, Marrakech, Morocco.
Cadi Ayyad University, Faculty of Sciences Semlalia, Neurosciences, Pharmacology and Environment Unit, Avenue My Abdellah, B.P. 2390, Marrakech, Morocco; Cadi Ayyad University, Multidisciplinary Faculty of Safi, Department of Biology, Safi, Morocco.
C R Biol. 2019 Jun-Aug;342(5-6):192-198. doi: 10.1016/j.crvi.2019.07.004. Epub 2019 Aug 29.
Exposure to lead is a threat factor for neurodegenerative disorders progress as it could trigger dopaminergic deficiency. We aimed herein to assess the effect of acute lead exposure (25mg/kg B.W i.p.) during three continuous days on the dopaminergic and noradrenergic systems together with locomotor performance in Meriones shawi (M. shawi), then the neuroprotective potential of curcumin-III (30mg/kg B.W) by oral gavage. Pb-exposed M. shawi exhibited increased tyrosine hydroxylase (TH) immunoreactivity in substantia nigra compacta (SNc), ventral tegmental area (VTA), locus coeruleus (LC), and dorsal striatum (DS), unlike the controls. This was correlated with decreased locomotor performance. A noticeable protective effect by co-treatment with curcumin-III was observed; in consequence, TH-immunoreactivity and locomotor disturbance were restored in Pb-treated Meriones. Our data results proved, on the one hand, an evident neurotoxic effect of acute Pb exposure and, on the other hand, a potent therapeutic effect of curcumin-III. Thereby, this compound may be recommended as a neuroprotective molecule for neurodegenerative disorders involving catecholaminergic impairment initiated by metallic elements.
铅暴露是神经退行性疾病进展的威胁因素,因为它可能引发多巴胺能缺乏。我们旨在评估连续三天腹腔注射 25mg/kg 体重的急性铅暴露对麦哲伦沙维氏鼠(M. shawi)的多巴胺能和去甲肾上腺素能系统以及运动表现的影响,然后通过口服灌胃评估姜黄素-III(30mg/kg 体重)的神经保护潜力。与对照组相比,暴露于铅的麦哲伦沙维氏鼠的黑质致密部(SNc)、腹侧被盖区(VTA)、蓝斑核(LC)和背侧纹状体(DS)中的酪氨酸羟化酶(TH)免疫反应性增加。这与运动表现下降有关。用姜黄素-III 联合治疗观察到明显的保护作用;因此,Pb 处理的麦哲伦沙维氏鼠的 TH-免疫反应性和运动障碍得到恢复。我们的数据结果一方面证明了急性 Pb 暴露的明显神经毒性作用,另一方面证明了姜黄素-III 的强大治疗作用。因此,该化合物可被推荐为涉及金属元素引发的儿茶酚胺能损伤的神经退行性疾病的神经保护分子。