Jadhav Ratnakar, Kulkarni Yogesh A
Shobhaben Pratapbhai Patel School of Pharmacy & Technology Management, SVKM's NMIMS, V.L. Mehta Road, Vile Parle (West), Mumbai 400056, India.
Antioxidants (Basel). 2023 Mar 13;12(3):707. doi: 10.3390/antiox12030707.
Alzheimer's disease (AD) is a neuronal condition causing progressive loss of memory and cognitive dysfunction particularly in elders. An upsurge in the global old age population has led to a proportionate increase in the prevalence of AD. The current treatments for AD are symptomatic and have debilitating side effects. A literature review and current research have directed scientists to explore natural products with better safety and efficacy profiles as new treatment options for AD. Baicalein, belonging to the flavone subclass of flavonoids, has been reported for its anti-oxidant, anti-inflammatory, AChE enzyme inhibitory activity and anti-amyloid protein aggregation activity, which collectively demonstrates its benefits as a neuroprotective agent. Presently, memantine, a NMDAR antagonist, is one of the important drugs used for treatment of Alzheimer's disease. The current study aims to investigate the effect of baicalein in combination with memantine in β-amyloid-induced AD in albino Wistar rats. Baicalein (10 mg/kg) alone, 5 mg/kg and 10 mg/kg in combination with memantine (20 mg/kg) was administered for 21 days. Treatment with baicalein in combination with memantine showed significant improvement in behavioural studies. The combination treatment decreased oxidative stress, β-amyloid plaque formation and increased the expression of brain-derived neurotrophic factor (BDNF) in the brain. From the results, it can be concluded that treatment with baicalein and memantine could be beneficial for reducing the progression of neurodegeneration in rats. Baicalein has an additive effect in combination with memantine, making it a potential option for the treatment of AD.
阿尔茨海默病(AD)是一种导致记忆力逐渐丧失和认知功能障碍的神经疾病,尤其在老年人中更为常见。全球老年人口的增加导致AD患病率相应上升。目前AD的治疗方法只是对症治疗,且有令人虚弱的副作用。文献综述和当前研究引导科学家探索具有更好安全性和有效性的天然产物作为AD的新治疗选择。黄芩素属于黄酮类的黄酮子类,据报道具有抗氧化、抗炎、乙酰胆碱酯酶抑制活性和抗淀粉样蛋白聚集活性,这些特性共同表明其作为神经保护剂的益处。目前,美金刚,一种N-甲基-D-天冬氨酸受体(NMDAR)拮抗剂,是用于治疗阿尔茨海默病的重要药物之一。本研究旨在探讨黄芩素与美金刚联合使用对白化Wistar大鼠β-淀粉样蛋白诱导的AD的影响。单独给予黄芩素(10mg/kg)、5mg/kg和10mg/kg与美金刚(20mg/kg)联合给药,持续21天。黄芩素与美金刚联合治疗在行为学研究中显示出显著改善。联合治疗降低了氧化应激、β-淀粉样蛋白斑块形成,并增加了大脑中脑源性神经营养因子(BDNF)的表达。从结果可以得出结论,黄芩素和美金刚联合治疗可能有助于减少大鼠神经退行性变的进展。黄芩素与美金刚联合使用具有相加作用,使其成为治疗AD的潜在选择。