Chitkara College of Pharmacy, Chitkara University, Punjab, India.
Department of Pharmacy, Southeast University, Banani, Dhaka 1213, Bangladesh.
Biomed Pharmacother. 2021 Aug;140:111729. doi: 10.1016/j.biopha.2021.111729. Epub 2021 May 25.
Neurodegenerative diseases (NDDs) are the primary cause of disabilities in the elderly people. Growing evidence indicates that oxidative stress, mitochondrial dysfunction, neuroinflammation and apoptosis are associated with aging and the basis of most neurodegenerative disorders. Quercetin is a flavonoid with significant pharmacological effects and promising therapeutic potential. It is widely distributed among plants and typically found in daily diets mainly in fruits and vegetables. It shows a number of biological properties connected to its antioxidant activity. Neuroprotection by quercetin has been reported in many in vitro as well as in in vivo studies. However, the exact mechanism of action is still mystery and similarly there are a number of hypothesis exploring the mechanism of neuroprotection. Quercetin enhances neuronal longevity and neurogenesis by modulating and inhibiting wide number of pathways. This review assesses the food sources of quercetin, its pharmacokinetic profile, structure activity relationship and its pathophysiological role in various NDDs and it also provides a synopsis of the literature exploring the relationship between quercetin and various downstream signalling pathways modulated by quercetin for neuroprotection for eg. nuclear factor erythroid 2-related factor 2 (Nrf2), Paraoxonase-2 (PON2), c-Jun N-terminal kinase (JNK), Tumour Necrosis Factor alpha (TNF-α), Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha (PGC-1α), Sirtuins, Mitogen-activated protein kinases (MAPKs) signalling cascades, CREB (Cyclic AMP response element binding protein) and Phosphoinositide 3- kinase(PI3K/Akt). Therefore, the aim of the present review was to elaborate on the cellular and molecular mechanisms of the quercetin involved in the protection against NDDs.
神经退行性疾病(NDDs)是老年人残疾的主要原因。越来越多的证据表明,氧化应激、线粒体功能障碍、神经炎症和细胞凋亡与衰老有关,是大多数神经退行性疾病的基础。槲皮素是一种具有显著药理作用和有前途的治疗潜力的类黄酮。它广泛分布于植物中,通常存在于水果和蔬菜等日常饮食中。它表现出许多与其抗氧化活性有关的生物学特性。槲皮素在许多体外和体内研究中都显示出神经保护作用。然而,其确切的作用机制仍然是个谜,同样有许多假说探索其神经保护作用的机制。槲皮素通过调节和抑制多种途径来增强神经元的寿命和神经发生。这篇综述评估了槲皮素的食物来源、药代动力学特征、构效关系及其在各种 NDDs 中的病理生理学作用,还综述了探索槲皮素与各种下游信号通路之间关系的文献,这些信号通路受槲皮素调节,以实现神经保护作用,例如核因子红细胞 2 相关因子 2(Nrf2)、对氧磷酶-2(PON2)、c-Jun N 末端激酶(JNK)、肿瘤坏死因子-α(TNF-α)、过氧化物酶体增殖物激活受体 γ 共激活因子 1-α(PGC-1α)、沉默调节蛋白、丝裂原激活蛋白激酶(MAPKs)信号级联、环腺苷酸反应元件结合蛋白(CREB)和磷酸肌醇 3-激酶(PI3K/Akt)。因此,本综述的目的是详细阐述槲皮素在保护 NDDs 中涉及的细胞和分子机制。