Department of Biology, School of Sciences and Engineering, The American University in Cairo, Cairo, 11835, Egypt.
Department of Zoology, Faculty of Science, Ain Shams University, Cairo, Egypt.
BMC Pharmacol Toxicol. 2023 Feb 23;24(1):11. doi: 10.1186/s40360-023-00651-4.
Neurotoxicity is a severe side effect of platinum compounds used for cancer chemotherapy such as Cisplatin. This neurotoxicity leads to severe cognitive and nervous dysfunction, therefore, limiting the dose of Cisplatin and compromising the treatment protocol.The present study investigates the neuroprotective effect of Sea Urchins which is a marine animal known for its rich bioactive compounds. Male Sprague Dawley rats received Cisplatin (2 mg/kg body weight) for 4 weeks, two times per week, followed by Sea Urchin extracts (50 and 100 mg/kg body weight) twice weekly for 4 weeks.Results show that rats treated with Urchin's extracts showed a significant improvement in the thermal (heat and cold) sensitivity compared to untreated rats. Liver enzymes Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) and Urea levels were also significantly decreased back to normal following treatment with sea urchin extracts. Brain tissue oxidative stress marker Nitric oxide (NO) and lipid peroxidation marker Malondialdehyde (MDA) increased significantly in the cisplatin-treated rats while the reduced glutathione levels (GSH) and catalase activity (CAT) showed a significant decrease. Treatment with sea Urchin extracts reversed these changes.Histological and immunohistochemical examination of the cerebral cortex reveled degenerative changes such as karyopyknosis and shrunken necrotic ghost like neurons in the cisplatin treated groups. There was also strong positive Glial fibrillary acidic protein (GFAP) reactivity and a negative B-cell leukemia/lymphoma 2 protein (Bcl2) reaction in most apparent neurons, indicating strong apoptotic changes. Treatment with Urchin extracts reversed these changes. Quantification of cerebral cortex neurons also revealed the strong effect of the extracts. Cisplatin treated groups showed 3708 cells/ mm3 compared to 8091 cells/mm in the normal rats. Extract treatment increased the neuronal numbers to almost normal levels. Quantification of the Immuno-histochemical expression of GFAP showed an increase by 10-folds after cisplatin administration. A remarkable decline from the cisplatin group was seen in the extract treated groups.In Conclusion, Sea Urchins extracts possess a strong neuroprotective activity and could provide a novel therapeutic method to prevent Cisplatin-induced neurotoxicity.
神经毒性是顺铂等用于癌症化疗的铂化合物的严重副作用。这种神经毒性导致严重的认知和神经功能障碍,因此限制了顺铂的剂量,并影响了治疗方案。本研究调查了海胆的神经保护作用,海胆是一种以其丰富的生物活性化合物而闻名的海洋动物。雄性 Sprague Dawley 大鼠每周两次接受顺铂(2mg/kg 体重)治疗 4 周,然后每周两次接受海胆提取物(50 和 100mg/kg 体重)治疗 4 周。结果表明,与未治疗的大鼠相比,用海胆提取物治疗的大鼠在热(热和冷)敏感性方面有显著改善。肝酶丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)以及尿素水平在海胆提取物治疗后也显著恢复正常。与顺铂治疗组相比,脑组织氧化应激标志物一氧化氮(NO)和脂质过氧化标志物丙二醛(MDA)显著增加,而还原型谷胱甘肽(GSH)和过氧化氢酶活性(CAT)则显著降低。用海胆提取物治疗逆转了这些变化。大脑皮质的组织学和免疫组织化学检查显示,在顺铂治疗组中出现退行性变化,如核固缩和皱缩的坏死样神经元。星形胶质细胞纤维酸性蛋白(GFAP)反应也很强,大多数明显神经元的 B 细胞白血病/淋巴瘤 2 蛋白(Bcl2)反应为阴性,表明强烈的凋亡变化。用海胆提取物治疗逆转了这些变化。大脑皮质神经元的定量分析也显示了提取物的强烈作用。顺铂治疗组的细胞数为 3708 个/ mm3,而正常大鼠为 8091 个/ mm3。提取物治疗使神经元数量几乎恢复正常水平。星形胶质细胞纤维酸性蛋白免疫组织化学表达的定量分析显示,顺铂给药后增加了 10 倍。在提取物治疗组中,从顺铂组观察到明显下降。总之,海胆提取物具有很强的神经保护活性,可以为预防顺铂引起的神经毒性提供一种新的治疗方法。