Camila de Oliveira Vian, Marcelo Augusto Germani Marinho, Magno da Silva Marques, Mariana Appel Hort, Marcos Freitas Cordeiro, Ana Paula Horn
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引用次数: 0
摘要
帕金森病(PD)是一种神经退行性疾病,会影响多巴胺能神经元,从而损害多巴胺能信号传导。槲皮素(QUE)具有抗氧化和神经保护特性,有望用于帕金森病的治疗。本系统综述旨在研究槲皮素在临床前模型中对帕金森病的治疗效果。系统性检索在 PubMed、Scopus 和 Web of Science 上进行。在最后的筛选阶段,根据预先确定的标准选出了 26 篇文章。入选的研究采用了不同的诱导帕金森病的方法和动物模型。大多数研究使用了大鼠(73.08%)和小鼠(23.08%),6-OHDA是诱导帕金森病的主要策略(38.6%),其次是鱼藤酮(30.8%)。对浸泡在油、纳米系统或游离制剂中的 QUE 进行了测试,给药途径和剂量各不相同,口服和腹腔给药剂量分别为 10 至 400 毫克/千克和 5 至 200 毫克/千克。总之,已发表数据的证据表明,QUE可用于治疗帕金森病,主要是通过抑制氧化应激、神经炎症反应和细胞凋亡途径。
Effects of quercetin in preclinical models of Parkinson's disease: A systematic review
Parkinson's disease (PD) is a neurodegenerative disease that affects dopaminergic neurons, thus impairing dopaminergic signalling. Quercetin (QUE) has antioxidant and neuroprotective properties that are promising for the treatment of PD. This systematic review aimed to investigate the therapeutic effects of QUE against PD in preclinical models. The systematic search was performed in PubMed, Scopus and Web of Science. At the final screening stage, 26 articles were selected according to pre-established criteria. Selected studies used different methods for PD induction, as well as animal models. Most studies used rats (73.08%) and mice (23.08%), with 6-OHDA as the main strategy for PD induction (38.6%), followed by rotenone (30.8%). QUE was tested immersed in oil, nanosystems or in free formulations, in varied routes of administration and doses, ranging from 10 to 400 mg/kg and from 5 to 200 mg/kg in oral and intraperitoneal administrations, respectively. Overall, evidence from published data suggests a potential use of QUE as a treatment for PD, mainly through the inhibition of oxidative stress, neuroinflammatory response and apoptotic pathways.
期刊介绍:
Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.