熊果酸:治疗中枢神经系统疾病的药理作用的历史方面

V. Ansari, Aditya Singh, Tarique Mahmood, Farogh Ahsan, Rufaida Wasim, M. Shariq, S. Parveen, Arshiya Shamim
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引用次数: 0

摘要

熊果酸(UA)已被用于改善与记忆相关的认知过程和智力功能。本研究旨在探讨UA的民族植物学用途、植物化学成分、毒性和中枢神经系统活性。根据药理学研究,它能促进学习和记忆,并对阿尔茨海默病、帕金森病和认知障碍具有生物效应。在任何试验剂量下,UA均未引起任何死亡、体重异常或病理疾病。此外,没有行为学、神经毒素、凝血学、血液学或临床化学变化被视为UA治疗的结果。UA也被用作药妆产品,改善皮肤功能。本文考察了目前可用的所有知识,揭示了基于数据对电流的化学成分进行了广泛研究,从而获得了具有改进效力、生物利用度和稳定性的UA衍生物,用于治疗许多非传染性疾病。UA的药理活性已被用于改善学习和记忆,治疗抑郁症、情绪压力、疲劳、焦虑、失眠、阿尔茨海默病、帕金森病、癫痫和精神分裂症。本综述详细介绍了UA对中枢神经系统的影响。大多数UA研究都是对中枢神经系统细胞机制的临床前评估,需要更多的转化临床研究来评估药物的安全性和有效性,以及其良好的生物分布,可以通过不同的途径和给药途径进行靶向。一些体外和体内研究已经调查了UA的药理学特性,报告了神经保护作用和认知功能的改善。这些作用归因于其抗氧化、抗细胞凋亡和抗炎作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ursolic acid: Historical aspects to promising pharmacological actions for the treatment of central nervous system diseases
Ursolic acid (UA) has been utilized to improve memory-related cognitive processes and intellectual functions. This study aims to examine the ethnobotanical uses, phytochemical composition, toxicity, and central nervous system activities of UA. It promotes learning and memory and has biological effects against Alzheimer's disease, Parkinson's disease, and cognitive impairment, according to pharmacological investigations. UA did not cause any death, abnormal body weight, or pathological diseases at any of the test doses. Furthermore, no behavioral, neurotoxin, coagulation, haematological, or clinical chemistry changes were seen as a result of UA treatment. UA is also used as a cosmeceutical product to improve skin functions. This article examines all knowledge that has become available at this time for revealing the chemistry of the current has been extensively investigated based on the data, resulting in UA derivatives with improved potency, bioavailability, and stability being used to treat a number of non-communicable diseases. The pharmacological activity of UA has been exploited to improve learning and memory and treat depression, emotional stress, fatigue, anxiety, insomnia, Alzheimer’s disease, Parkinson’s disease, epilepsy, and schizophrenia. The effects of UA on the central nervous system detailed in this review. The majority of UA studies have been preclinical evaluations of cellular mechanisms in the central nervous system, and more translational clinical research is needed to assess the drug's safety and efficacy, as well as its favorable, biodistribution, which could be targeted using different pathways and administration routes. Several in vitro and in vivo studies have investigated the pharmacological properties of UA reporting neuroprotective effects and improvements in cognitive function. These effects are attributed to its antioxidant, antiapoptotic, and anti-inflammatory actions.
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