Evidence map›Paper›PMID 37185136›Full record

ArticleStroke and vascular neurology2023

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

Haiyin Wu, Zhenquan Huang, Xuan Wang, Mingyu Chen, Wei Chen, Yao Hua, Jian Ren, Luyao Shen, Yixuan Song, Ying Zhou and 6 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Stroke and vascular neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06770491 (A Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Phase 1 Study to Assess the Safety, Tolerability, and Pharmacokinetic Profiles of Y-3 in Healthy Adult Volunteers in the United States), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06770491 phase1completednot on this mapstarted 2025, after this paper: background citation

A Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Phase 1 Study to Assess the Safety, Tolerability, and Pharmacokinetic Profiles of Y-3 in Healthy Adult Volunteers in the United States

TypeinterventionalSponsorNeurodawn Pharmaceutical Co., Ltd.Ran2025 to 2025Enrolled20ConditionsSafety, Tolerability, Pharmacokinetic Study in Healthy VolunteersArmsY-3 for injection, Placebo
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 2 institutions in 1 country.

Haiyin Wu *Department of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Zhenquan Huang *Department of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Xuan WangDepartment of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Mingyu ChenDepartment of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Wei ChenDepartment of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Yao HuaNeuroDawn Pharmaceutical Co., Ltd, Nanjing, China.
Jian RenNeuroDawn Pharmaceutical Co., Ltd, Nanjing, China.
Luyao ShenDepartment of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Yixuan SongDepartment of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Ying ZhouDepartment of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Chunxia LuoDepartment of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.ORCID 0000-0002-9840-0402
Yuhui LinDepartment of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Yilong WangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.ORCID 0000-0002-3267-0039
Lei ChangDepartment of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China dyzhu@njmu.edu.cn kldlf@njmu.edu.cn leichang@njmu.edu.cn.
Fei LiDepartment of Medicinal Chemistry, School of Pharmacy, Nanjing Medical University, Nanjing, China dyzhu@njmu.edu.cn kldlf@njmu.edu.cn leichang@njmu.edu.cn.
Dongya ZhuDepartment of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China dyzhu@njmu.edu.cn kldlf@njmu.edu.cn leichang@njmu.edu.cn.ORCID 0000-0002-2145-0225
Nanjing Medical University · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPoststroke 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.

methodsPhotothrombotic 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.

resultsAdministration 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.

conclusionZL006-05 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.

Indexed as

Anti-Anxiety AgentsStrokeAnimalsAntidepressive AgentsAnxietyBrainMiceRatsAnti-Anxiety AgentsAntidepressive AgentsBrainCerebral InfarctionPharmacologyStroke

Identifiers

PMID37185136
PMCPMC10800258
OpenAlexW4366992142

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.