Królicka Ewelina, Kieć-Kononowicz Katarzyna, Łażewska Dorota
Department of Technology and Biotechnology of Drugs, Faculty of Pharmacy, Jagiellonian University Medical College, Medyczna 9, 30-688 Kraków, Poland.
Pharmaceuticals (Basel). 2022 Jul 10;15(7):847. doi: 10.3390/ph15070847.
Along with the increase in life expectancy, a significant increase of people suffering from neurodegenerative diseases (ND) has been noticed. The second most common ND, after Alzheimer's disease, is Parkinson's disease (PD), which manifests itself with a number of motor and non-motor symptoms that hinder the patient's life. Current therapies can only alleviate those symptoms and slow down the progression of the disease, but not effectively cure it. So now, in addition to understanding the mechanism and causes of PD, it is also important to find a powerful way of treatment. It has been proved that in the etiology and course of PD, the essential roles are played by dopamine (DA) (an important neurotransmitter), enzymes regulating its level (e.g., COMT, MAO), and oxidative stress leading to neuroinflammation. Chalcones, due to their "simple" structure and valuable biological properties are considered as promising candidates for treatment of ND, also including PD. Here, we provide a comprehensive review of chalcones and related structures as potential new therapeutics for cure and prevention of PD. For this purpose, three databases (Pubmed, Scopus and Web of Science) were searched to collect articles published during the last 5 years (January 2018-February 2022). Chalcones have been described as promising enzyme inhibitors (MAO B, COMT, AChE), -synuclein imaging probes, showing anti-neuroinflammatory activity (inhibition of iNOS or activation of Nrf2 signaling), as well as antagonists of adenosine A and/or A receptors. This review focused on the structure-activity relationships of these compounds to determine how a particular substituent or its position in the chalcone ring(s) (ring A and/or B) affects biological activity.
随着预期寿命的增加,人们注意到患有神经退行性疾病(ND)的人数显著增加。仅次于阿尔茨海默病的第二常见的神经退行性疾病是帕金森病(PD),它表现为多种运动和非运动症状,这些症状会妨碍患者的生活。目前的治疗方法只能缓解这些症状并减缓疾病的进展,但不能有效治愈。因此,现在除了了解帕金森病的机制和病因外,找到一种有效的治疗方法也很重要。事实证明,在帕金森病的病因和病程中,多巴胺(DA)(一种重要的神经递质)、调节其水平的酶(如儿茶酚-O-甲基转移酶、单胺氧化酶)以及导致神经炎症的氧化应激起着至关重要的作用。查耳酮由于其“简单”的结构和有价值的生物学特性,被认为是治疗包括帕金森病在内的神经退行性疾病的有希望的候选药物。在这里,我们对查耳酮及其相关结构作为治疗和预防帕金森病的潜在新疗法进行了全面综述。为此,我们检索了三个数据库(PubMed、Scopus和Web of Science),以收集过去5年(2018年1月至2022年2月)发表的文章。查耳酮已被描述为有希望的酶抑制剂(单胺氧化酶B、儿茶酚-O-甲基转移酶、乙酰胆碱酯酶)、α-突触核蛋白成像探针,具有抗神经炎症活性(抑制诱导型一氧化氮合酶或激活核因子E2相关因子2信号通路),以及腺苷A2A和/或A1受体拮抗剂。本综述重点关注这些化合物的构效关系,以确定查耳酮环(A环和/或B环)中特定取代基或其位置如何影响生物活性。