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将度洛西汀重新用作一种强效丁酰胆碱酯酶抑制剂:对患有抑郁症和认知障碍的老年人潜在的胆碱能增强益处。

Repurposing Duloxetine as a Potent Butyrylcholinesterase Inhibitor: Potential Cholinergic Enhancing Benefits for Elderly Individuals with Depression and Cognitive Impairment.

作者信息

Darreh-Shori Taher, Baidya Anurag T K, Brouwer Medea, Kumar Amit, Kumar Rajnish

机构信息

Division of Clinical Geriatrics, Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, NEO, Seventh Floor, 141 52 Stockholm, Sweden.

Department of Pharmaceutical Engineering & Technology, Indian Institute of Technology (B.H.U.), Varanasi 221005, Uttar Pradesh, India.

出版信息

ACS Omega. 2024 Aug 21;9(35):37299-37309. doi: 10.1021/acsomega.4c05089. eCollection 2024 Sep 3.

Abstract

Despite the advent of new treatment strategies, cholinesterase inhibitors (ChEIs) are still the go-to treatment for dementia disorders. ChEIs act by inhibiting the main acetylcholine-degrading enzyme, acetylcholinesterase (AChE). Nonetheless, accumulating evidence indicates that the impact of inhibition of the sister enzyme, butyrylcholinesterase (BChE), could be even broader in older adults due to the multifaceted role of BChE in several biological functional pathways. Therefore, we employed an modeling-based drug repurposing strategy to identify novel potent BChE inhibitors from the FDA drug database. This was followed by screening and enzyme kinetic validation using human plasma samples as the source of BChE. The analysis revealed that the antidepressant drug, duloxetine, inhibited BChE with high selectivity in comparison to AChE. In contrast, two other antidepressants, namely, citalopram and escitalopram exhibited a weak to moderate activity. enzyme inhibition kinetic analyses indicated that duloxetine acted as a competitive inhibitor of BChE with an inhibition constant ( ) of 210 nM. This value is comparable with 100-400 nM concentration of duloxetine following normal dosages in humans, thereby indicating that duloxetine should be able to induce a pharmacologically and biologically relevant inhibition of BChE. Additionally, we performed the enzyme inhibition kinetic assessment in parallel for ethopropazine, a known potent selective BChE inhibitor, and physostigmine, a dual inhibitor of AChE and BChE. These analyses indicated that duloxetine should be considered a potent BChE inhibitor since its was comparable with ethopropazine ( = 150 nM) but was 4 times smaller than that of physostigmine ( 840 nM). In conclusion, this study reports the discovery of duloxetine being a highly potent selective competitive BChE inhibitor. This, in turn, indicates that duloxetine could be the choice of antidepressive treatment in older adults with both depressive and dementia symptoms since it may offer additional clinically beneficial effects this secondary mode of cholinergic enhancing action.

摘要

尽管出现了新的治疗策略,但胆碱酯酶抑制剂(ChEIs)仍然是痴呆症疾病的首选治疗方法。ChEIs通过抑制主要的乙酰胆碱降解酶乙酰胆碱酯酶(AChE)发挥作用。然而,越来越多的证据表明,由于丁酰胆碱酯酶(BChE)在多种生物功能途径中的多方面作用,抑制这种姐妹酶对老年人的影响可能更为广泛。因此,我们采用基于模型的药物重新利用策略,从美国食品药品监督管理局(FDA)药物数据库中识别新型强效BChE抑制剂。随后,以人血浆样本作为BChE的来源进行筛选和酶动力学验证。分析表明,与AChE相比,抗抑郁药度洛西汀对BChE具有高选择性抑制作用。相比之下,另外两种抗抑郁药西酞普兰和艾司西酞普兰表现出弱至中等活性。酶抑制动力学分析表明,度洛西汀作为BChE的竞争性抑制剂,抑制常数( )为210 nM。该 值与人类正常剂量下100 - 400 nM浓度的度洛西汀相当,从而表明度洛西汀应该能够诱导对BChE具有药理学和生物学相关性的抑制作用。此外,我们同时对已知的强效选择性BChE抑制剂乙磺半胱氨酸和AChE与BChE的双重抑制剂毒扁豆碱进行了酶抑制动力学评估。这些分析表明,度洛西汀应被视为一种强效BChE抑制剂,因为其 与乙磺半胱氨酸( = 150 nM)相当,但比毒扁豆碱( 840 nM)小4倍。总之,本研究报告发现度洛西汀是一种高效的选择性竞争性BChE抑制剂。这反过来表明,度洛西汀可能是患有抑郁和痴呆症状的老年人抗抑郁治疗的选择,因为它可能通过这种胆碱能增强作用的次要模式提供额外的临床有益效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4259/11375813/a164a03cd833/ao4c05089_0001.jpg

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