Preclinical evaluation of ZL006-05, a new antistroke drug with fast-onset antidepressant and anxiolytic effects.

IF 4.4 1区 医学 Q1 CLINICAL NEUROLOGY
Haiyin Wu, Zhenquan Huang, Xuan Wang, Mingyu Chen, Wei Chen, Yao Hua, Jian Ren, Luyao Shen, Yixuan Song, Ying Zhou, Chunxia Luo, Yuhui Lin, Yilong Wang, Lei Chang, Fei Li, Dongya Zhu
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引用次数: 0

Abstract

Background: Poststroke depression and anxiety, independent predictor of poor functional outcomes, are common in the acute phase of stroke. Up to now, there is no fast-onset antidepressive and anxiolytic agents suitable for the management of acute stroke. ZL006-05, a dual-target analgesic we developed, dissociates nitric oxide synthase from postsynaptic density-95 while potentiates α2-containing γ-aminobutyric acid type A receptor. This study aims to determine whether ZL006-05 can be used as an antistroke agent with fast-onset antidepressant and anxiolytic effects.

Methods: Photothrombotic stroke and transient middle cerebral artery occlusion were induced in rats and mice. Infarct size was measured by TTC(2,3,5-Triphenyltetrazolium chloride) staining or Nissl staining. Neurological defects were assessed by four-point scale neurological score or modified Neurological Severity Scores. Grid-walking, cylinder and modified adhesive removal tasks were conducted to assess sensorimotor functions. Spatial learning was assessed using Morris water maze task. Depression and anxiety were induced by unpredictable chronic mild stress. Depressive behaviours were assessed by tail suspension, forced swim and sucrose preference tests. Anxiety behaviours were assessed by novelty-suppressed feeding and elevated plus maze tests. Pharmacokinetics, toxicokinetics and long-term toxicity studies were performed in rats.

Results: Administration of ZL006-05 in the acute phase of stroke attenuated transient and permanent ischaemic injury and ameliorated long-term functional impairments significantly, with a treatment window of 12 hours after ischemia, and reduced plasminogen activato-induced haemorrhagic transformation. ZL006-05 produced fast-onset antidepressant and anxiolytic effects with onset latency of 1 hour in the normal and CMS mice, had antidepressant and anxiolytic effects in stroke mice. ZL006-05 crossed the blood-brain barrier and distributed into the brain rapidly, and had a high safety profile in toxicokinetics and long-term toxicological studies.

Conclusion: ZL006-05 is a new neuroprotectant with fast-onset antidepressant and anxiolytic effects and has translational properties in terms of efficacy, safety and targeting of clinical issues.

具有快速起效抗抑郁和抗焦虑作用的新型抗中风药物 ZL006-05 的临床前评估。
背景:卒中后抑郁和焦虑是卒中急性期常见的不良功能预后的独立预测因素。迄今为止,还没有适合急性中风治疗的快速起效抗抑郁和抗焦虑药物。ZL006-05是我们开发的一种双靶点镇痛药,它能使一氧化氮合酶与突触后密度-95分离,同时增强含α2的γ-氨基丁酸A型受体的作用。本研究旨在确定 ZL006-05 是否可用作具有快速起效抗抑郁和抗焦虑作用的抗中风药物:方法:诱导大鼠和小鼠发生光栓性中风和一过性大脑中动脉闭塞。用 TTC(2,3,5-三苯基氯化四氮唑)染色法或 Nissl 染色法测量梗死面积。神经系统缺陷通过四级神经系统评分或改良神经系统严重程度评分进行评估。通过网格行走、圆柱体和改良粘合剂去除任务来评估感觉运动功能。使用莫里斯水迷宫任务评估空间学习能力。抑郁和焦虑由不可预测的慢性轻度压力诱发。抑郁行为通过悬尾、强迫游泳和蔗糖偏好测试进行评估。焦虑行为通过新奇抑制喂食和高架加迷宫测试进行评估。对大鼠进行了药代动力学、毒代动力学和长期毒性研究:结果:在脑卒中急性期服用 ZL006-05 可减轻短暂性和永久性缺血损伤,显著改善长期功能障碍,治疗窗口期为缺血后 12 小时,并可减少纤溶酶原激活剂诱导的出血转化。ZL006-05对正常小鼠和CMS小鼠具有快速起效的抗抑郁和抗焦虑作用,起效潜伏期为1小时,对中风小鼠具有抗抑郁和抗焦虑作用。ZL006-05能穿过血脑屏障并迅速分布到大脑中,在毒代动力学和长期毒理学研究中具有较高的安全性:结论:ZL006-05是一种新型神经保护剂,具有快速起效的抗抑郁和抗焦虑作用,在疗效、安全性和针对临床问题方面具有转化特性。
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来源期刊
Stroke and Vascular Neurology
Stroke and Vascular Neurology Medicine-Cardiology and Cardiovascular Medicine
CiteScore
11.20
自引率
1.70%
发文量
63
审稿时长
15 weeks
期刊介绍: Stroke and Vascular Neurology (SVN) is the official journal of the Chinese Stroke Association. Supported by a team of renowned Editors, and fully Open Access, the journal encourages debate on controversial techniques, issues on health policy and social medicine.
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