Mahmoud Abdulla M A, Mantawy Eman M, Wahdan Sara A, Ammar Ramy M, El-Demerdash Ebtehal
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Badr University in Cairo (BUC), Cairo, Egypt.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.
Biomed Pharmacother. 2023 Mar;159:114238. doi: 10.1016/j.biopha.2023.114238. Epub 2023 Jan 12.
Cisplatin (CP) is a broad-spectrum antineoplastic agent used to treat many human cancers. Nonetheless, most patients receiving CP suffer from cognitive deficits, a phenomenon termed "chemo-brain". Recently, vildagliptin (Vilda), a DPP-4 inhibitor, has demonstrated promising neuroprotective properties against various neurological diseases. Therefore, the present study aims to investigate the potential neuroprotective properties of Vilda against CP-induced neurotoxicity and elucidate the underlying molecular mechanisms. Chemo-brain was induced in Sprague-Dawley rats by i.p injection of CP at a dose of 5 mg/kg once weekly for four weeks. Vilda was administered daily at a dose (10 mg/kg; P.O) for four weeks. The results revealed that Vilda restored the cognitive function impaired by CP, as assessed by the Morris water maze, Y-maze, and passive avoidance tests. Moreover, Vilda alleviated the CP-induced neurodegeneration, as shown by toluidine blue staining, besides markedly reduced amyloid plaque deposition, as evidenced by Congo red staining. Notably, Vilda boosted cholinergic neurotransmission through the downregulation of the acetylcholinesterase enzyme. In addition, the neuroprotective mechanisms of Vilda include diminishing oxidative stress by reducing MDA levels while raising GSH levels and SOD activity, repressing neuronal apoptosis as shown by elevated Bcl-2 levels together with diminished Bax and caspase-3 expressions, inhibiting neuroinflammation as shown by decreased GFAP expression, and finally boosting hippocampal neurogenesis and survival by upregulating expressions of BDNF and PCNA. These effects were mainly mediated by activating AMPK/Akt/CREB signaling cascades. In summary, Vilda can be considered a promising candidate for guarding against CP-induced chemo-brain and neurodegeneration, thus improving the quality of life of cancer patients.
顺铂(CP)是一种用于治疗多种人类癌症的广谱抗肿瘤药物。尽管如此,大多数接受CP治疗的患者都患有认知缺陷,这种现象被称为“化疗脑”。最近,二肽基肽酶-4(DPP-4)抑制剂维格列汀(Vilda)已显示出对各种神经疾病具有有前景的神经保护特性。因此,本研究旨在探讨Vilda对CP诱导的神经毒性的潜在神经保护特性,并阐明其潜在的分子机制。通过每周一次腹腔注射5mg/kg剂量的CP,连续四周,在Sprague-Dawley大鼠中诱导化疗脑。Vilda以10mg/kg的剂量(口服)每日给药,持续四周。结果显示,通过莫里斯水迷宫、Y迷宫和被动回避试验评估,Vilda恢复了CP受损的认知功能。此外,甲苯胺蓝染色显示Vilda减轻了CP诱导的神经退行性变,刚果红染色证明其还显著减少了淀粉样斑块沉积。值得注意的是,Vilda通过下调乙酰胆碱酯酶来增强胆碱能神经传递。此外,Vilda的神经保护机制包括通过降低丙二醛(MDA)水平同时提高谷胱甘肽(GSH)水平和超氧化物歧化酶(SOD)活性来减少氧化应激,通过提高Bcl-2水平同时降低Bax和半胱天冬酶-3(caspase-3)表达来抑制神经元凋亡,通过降低胶质纤维酸性蛋白(GFAP)表达来抑制神经炎症,最后通过上调脑源性神经营养因子(BDNF)和增殖细胞核抗原(PCNA)的表达来促进海马神经发生和存活。这些作用主要是通过激活腺苷酸活化蛋白激酶(AMPK)/蛋白激酶B(Akt)/环磷腺苷效应元件结合蛋白(CREB)信号级联介导的。总之,Vilda可被认为是预防CP诱导的化疗脑和神经退行性变的有前景的候选药物,从而改善癌症患者的生活质量。