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难治性双相情感障碍药物治疗的未来方向

Future Directions for Pharmacotherapies for Treatment-resistant Bipolar Disorder.

作者信息

Dodd Seetal, Fernandes Brisa S, Dean Olivia M

机构信息

IMPACT Strategic Research Centre, School of Medicine, Deakin University, Geelong, Victoria, Australia.

出版信息

Curr Neuropharmacol. 2015;13(5):656-62. doi: 10.2174/1570159x13666150630175841.

Abstract

Current pharmacological treatments for bipolar disorder (BD) are limited and efficacy has historically been discovered through serendipity. There is now scope for new drug development, focused on the underlying biology of BD that is not targeted by current therapies. The need for novel treatments is urgent when considering treatment resistant BD, where current therapies have failed. While established drugs targeting the monoamine systems continue to be worthwhile, new biological targets including inflammatory and oxidative an nitrosative pathways, apoptotic and neurotrophic pathways, mitochondrial pathways, the N-methyl-Daspartate (NMDA)-receptor complex, the purinergic system, neuropeptide system, cholinergic system and melatonin pathways are all being identified as potential anchors for the discovery of new agents. Many agents are experimental and efficacy data is limited, however further investigation may provide a new line for drug discovery, previously stalled by lack of corporate interest.

摘要

目前用于双相情感障碍(BD)的药物治疗有限,其疗效历来是偶然发现的。现在有新药研发的空间,重点是针对双相情感障碍目前疗法未针对的潜在生物学机制。考虑到难治性双相情感障碍(即当前疗法已失效),对新型治疗方法的需求迫在眉睫。虽然针对单胺系统的现有药物仍然有价值,但新的生物学靶点,包括炎症、氧化和亚硝化途径、凋亡和神经营养途径、线粒体途径、N-甲基-D-天冬氨酸(NMDA)受体复合物、嘌呤能系统、神经肽系统、胆碱能系统和褪黑素途径,都被确定为发现新药物的潜在关键因素。许多药物尚处于实验阶段,疗效数据有限,然而进一步研究可能为药物发现提供一条新途径,此前该领域因缺乏企业兴趣而停滞不前。

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