Kandiah Nagaendran, Pai Ming-Chyi, Senanarong Vorapun, Looi Irene, Ampil Encarnita, Park Kyung Won, Karanam Ananda Krishna, Christopher Stephen
Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital.
Duke-NUS, Graduate Medical School, Singapore.
Clin Interv Aging. 2017 Apr 18;12:697-707. doi: 10.2147/CIA.S129145. eCollection 2017.
Several studies have demonstrated clinical benefits of sustained cholinesterase inhibition with rivastigmine in Alzheimer's disease (AD) and Parkinson's disease dementia (PDD). Unlike donepezil and galantamine that selectively inhibit acetylcholinesterase (AChE; EC 3.1.1.7), rivastigmine is a unique cholinesterase inhibitor with both AChE and butyrylcholinesterase (BuChE; EC 3.1.1.8) inhibitory activity. Rivastigmine is also available as transdermal patch that has been approved by the US Food and Drug Administration for the treatment of mild, moderate, and severe AD as well as mild-to-moderate PDD. In this review, we explore the role of BuChE inhibition in addition to AChE inhibition with rivastigmine in the outcomes of cognition, global function, behavioral symptoms, and activities of daily living. Additionally, we review the evidence supporting the use of dual AChE-BuChE inhibitory activity of rivastigmine as a therapeutic strategy in the treatment of neurological disorders, with a focus on the role of rivastigmine in subcortical dementias such as vascular dementia (VaD) and PDD. Toward this objective, we performed a literature search in PubMed and Ovid with limits to articles published in the English language before June 2016. The available evidence from the literature suggests that the dual inhibition of AChE and BuChE may afford additional therapeutic potential of rivastigmine in subcortical dementias (subcortical VaD and PDD) with benefits on cognition and behavioral symptoms. Rivastigmine was found to specifically benefit executive dysfunction frequently observed in subcortical dementias; however, large randomized clinical studies are warranted to support these observations.
多项研究已证明,卡巴拉汀持续抑制胆碱酯酶对阿尔茨海默病(AD)和帕金森病痴呆(PDD)具有临床益处。与选择性抑制乙酰胆碱酯酶(AChE;EC 3.1.1.7)的多奈哌齐和加兰他敏不同,卡巴拉汀是一种独特的胆碱酯酶抑制剂,同时具有AChE和丁酰胆碱酯酶(BuChE;EC 3.1.1.8)抑制活性。卡巴拉汀也有透皮贴剂剂型,已获美国食品药品监督管理局批准用于治疗轻度、中度和重度AD以及轻度至中度PDD。在本综述中,我们探讨了卡巴拉汀除抑制AChE外,抑制BuChE在认知、整体功能、行为症状和日常生活活动结果方面的作用。此外,我们回顾了支持将卡巴拉汀的双重AChE - BuChE抑制活性作为治疗神经疾病的治疗策略的证据,重点关注卡巴拉汀在皮质下痴呆如血管性痴呆(VaD)和PDD中的作用。为实现这一目标,我们在PubMed和Ovid上进行了文献检索,检索范围限制在2016年6月之前发表的英文文章。文献中的现有证据表明,AChE和BuChE的双重抑制可能为卡巴拉汀在皮质下痴呆(皮质下VaD和PDD)中带来额外的治疗潜力,对认知和行为症状有益。发现卡巴拉汀对皮质下痴呆中常见的执行功能障碍具有特殊益处;然而,需要大型随机临床研究来支持这些观察结果。