Ali Alaa Emam, Elsherbiny Doaa Mokhtar, Azab Samar S, El-Demerdash Ebtehal
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.
Neurotoxicology. 2022 Jan;88:1-13. doi: 10.1016/j.neuro.2021.10.002. Epub 2021 Oct 14.
Cognitive impairment or "chemobrain" is a troublesome adverse effect which had been increasingly reported by cancer patients after doxorubicin (DOX) chemotherapy. Notably, Hypertension, a very common comorbidity in cancer patients, could pose a greater risk for negative cognitive outcomes. Amiloride (AML) is an antihypertensive, potassium-sparing diuretic that has been proven to be neuroprotective in different experimental models; this can be attributed to its ability to inhibit different ion transporters such as NaH exchanger (NHE), which upon excessive activation can result in intracellular cationic overload, followed by oxidative damage and cellular death. Accordingly, this study was designed to investigate the potential neuroprotective effect of AML against DOX-induced chemobrain and to elucidate possible underlying mechanisms. Briefly, Histopathological examination and neurobehavioral testing (Morris water maze, Y maze and passive avoidance test) showed that AML co-treatment (10 mg/kg/day) markedly attenuated DOX (2 mg/kg/week)-induced neurodegeneration and memory impairment after 4 weeks of treatments. We found that DOX administration up-regulated NHE expression and increased lactic acid content in the hippocampus which were markedly opposed by AML. Moreover, AML mitigated DOX-induced neuroinflammation and decreased hippocampal tumor necrosis factor-α level, nuclear factor kappa-B, and cyclooxygenase-2 expression. Additionally, AML counteracted DOX-induced hippocampal oxidative stress as indicated by normalized malondialdehyde and glutathione levels. Furthermore, AML halted DOX-induced hippocampal apoptosis as evidenced by decreased caspase-3 activity and lower cytochrome c immunoexpression. Our results in addition to the previously reported antitumor effects of AML and its ability to mitigate cancer resistance to DOX therapy could point toward possible new repositioning scenarios of the diuretic AML especially regarding hypertensive cancer patients.
认知障碍或“化疗脑”是一种棘手的不良反应,越来越多的癌症患者在接受多柔比星(DOX)化疗后报告出现这种情况。值得注意的是,高血压是癌症患者中非常常见的合并症,可能会给负面认知结果带来更大风险。氨氯吡咪(AML)是一种保钾利尿的抗高血压药物,已被证明在不同实验模型中具有神经保护作用;这可归因于其抑制不同离子转运体的能力,如钠氢交换体(NHE),过度激活时会导致细胞内阳离子过载,进而引发氧化损伤和细胞死亡。因此,本研究旨在探讨AML对DOX诱导的化疗脑的潜在神经保护作用,并阐明可能的潜在机制。简而言之,组织病理学检查和神经行为测试(莫里斯水迷宫、Y迷宫和被动回避试验)表明,在治疗4周后,AML联合治疗(10毫克/千克/天)显著减轻了DOX(2毫克/千克/周)诱导的神经退行性变和记忆损害。我们发现,DOX给药上调了海马体中NHE的表达并增加了乳酸含量,而AML对此有明显的对抗作用。此外,AML减轻了DOX诱导的神经炎症,并降低了海马体肿瘤坏死因子-α水平、核因子κB和环氧化酶-2的表达。此外,AML抵消了DOX诱导的海马体氧化应激,这通过丙二醛和谷胱甘肽水平的正常化得以体现。此外,AML阻止了DOX诱导的海马体细胞凋亡,这通过降低半胱天冬酶-3活性和降低细胞色素c免疫表达得以证明。我们的研究结果,除了之前报道的AML的抗肿瘤作用及其减轻癌症对DOX治疗耐药性的能力外,可能指向利尿剂AML可能的新的重新定位方案,特别是对于高血压癌症患者。