Department of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Department of Medicinal Chemistry, School of Pharmacy, Nanjing Medical University, Nanjing, China.
Stroke Vasc Neurol. 2023 Dec 29;8(6):463-474. doi: 10.1136/svn-2022-002156.
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.
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.
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.
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.
脑卒中后抑郁和焦虑是影响患者功能预后的独立危险因素,在脑卒中急性期较为常见。目前,尚无适合于脑卒中管理的快速起效的抗抑郁和抗焦虑药物。我们开发的双重作用靶点镇痛剂 ZL006-05,可使一氧化氮合酶从突触后密度-95 上解离,并增强含α2 的γ-氨基丁酸 A 型受体。本研究旨在探讨 ZL006-05 是否可作为一种具有快速起效抗抑郁和抗焦虑作用的新型抗脑卒中药物。
采用光凝血栓形成法和短暂性大脑中动脉闭塞法制作大鼠和小鼠脑卒中模型。采用 TTC(2,3,5-三苯基氯化四氮唑)染色或尼氏染色法测量脑梗死体积,采用 4 分制神经功能缺损评分或改良神经功能缺损评分法评估神经功能缺损,采用网格行走、转棒和改良粘取实验评估感觉运动功能,采用 Morris 水迷宫实验评估空间学习能力。采用不可预测性慢性轻度应激诱导抑郁和焦虑模型,通过悬尾、强迫游泳和糖水偏好实验评估抑郁样行为,通过新奇抑制性摄食和高架十字迷宫实验评估焦虑样行为。在大鼠中进行药代动力学、毒代动力学和长期毒性研究。
脑卒中急性期给予 ZL006-05 治疗可减轻短暂性和永久性缺血损伤,显著改善长期功能障碍,治疗窗为缺血后 12 小时,可减少纤溶酶原激活物诱导的出血性转化。ZL006-05 在正常和 CMS 小鼠中具有快速起效的抗抑郁和抗焦虑作用,其作用潜伏期为 1 小时,在脑卒中小鼠中也具有抗抑郁和抗焦虑作用。ZL006-05 可快速透过血脑屏障并分布到大脑中,在毒代动力学和长期毒性研究中具有良好的安全性。
ZL006-05 是一种具有快速起效抗抑郁和抗焦虑作用的新型神经保护剂,在疗效、安全性和针对临床问题的靶向性方面具有转化潜力。