Evidence map›Paper›PMID 37632679›Full record

ArticleMolecular neurobiology2024

Mechanism of Antidepressant Action of (2R,6R)-6-Hydroxynorketamine (HNK) and Its Compounds: Insights from Proteomic Analysis.

Chaohui Zhen, Chong Wang, Yanjun Ma, Yuli Pang, Feiyue Cai, Jiali Meng, Yuefei He, Ping Xiao, Jianxi Liu, Xi Mei and 6 more

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 58% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 8 institutions in 2 countries.

Chaohui ZhenDepartment of Surgery, The First Dongguan Affiliated Hospital of Guangdong Medical University, Dongguan City, 523000, Guangdong Province, China.
Chong WangDepartment of Neurosurgery, Shenzhen Children's Hospital, Shenzhen City, 518026, Guangdong Province, China.
Yanjun MaShenzhen Ruijian Biotechnology Co., Ltd, Shenzhen City, 518057, Guangdong Province, China.
Yuli PangHealth Management Center, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen City, 518055, Guangdong Province, China.
Feiyue CaiHealth Management Center, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen City, 518055, Guangdong Province, China.
Jiali MengGeneral Practice Alliance, Shenzhen City, Guangdong Province, China.
Yuefei HeGeneral Practice Alliance, Shenzhen City, Guangdong Province, China.
Ping XiaoDepartment of Otorhinolaryngology Head and Neck Surgery, Shenzhen Children's Hospital, Shenzhen City, 518026, Guangdong Province, China.
Jianxi LiuShenzhen Ruijian Biotechnology Co., Ltd, Shenzhen City, 518057, Guangdong Province, China.
Xi MeiZhuhai Pengkun Biomedicine Technology Co. Ltd, Zhuhai City, 519000, Guangdong Province, China.
Shupeng LiState Key Laboratory of Oncogenomics, School of Chemical Biology and Biotechnology, Peking University, Shenzhen City, 518055, Guangdong Province, China.
Guanzheng WuCollege of Textiles and Clothing, Yancheng Institute of Technology, Yancheng City, 224051, Jiangsu Province, China.
Guangzhen JinInstitute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan, 31116, Korea.
Biao ZhengDepartment of Surgery, The First Dongguan Affiliated Hospital of Guangdong Medical University, Dongguan City, 523000, Guangdong Province, China. zhengbiao@gdmu.edu.cn.
Rui LiangDepartment of Surgery, The First Dongguan Affiliated Hospital of Guangdong Medical University, Dongguan City, 523000, Guangdong Province, China. lr9311038@163.com.
Zhen TanDepartment of Surgery, The First Dongguan Affiliated Hospital of Guangdong Medical University, Dongguan City, 523000, Guangdong Province, China. tanzhen@szu.edu.cn.ORCID http://orcid.org/0000-0002-0187-6755
Guangdong Medical College · CNShenzhen University · CNBeike Biotechnology (China) · CNShenzhen Children's Hospital · CNDankook University · KRPeking University · CNYancheng Institute of Technology · CNZhuhai Institute of Advanced Technology · CN

Funding

Shenzhen Health Elite Talent Project No.2021XKQ193Supported by Natural Scicence Foundation of Shenzhen University General Hospital SUGH2020QD015Supported by Shenzhen Natural Science Fund(the Stable Support Plan Program 20200826225552001
6 · The paper itself

Abstract

The effects of HNK, I5, and I6 on the expression of protein in hippocampus of depressed mice were studied by isobaric tags for relative and absolute quantitation (iTRAQ) to explore the mechanism of their antidepressant action. HNK, I5, and I6 were administered intragastric administration once a day in the morning for 7 days. The drug was subsequently discontinued for 7 days (without any treatment). On the 15th day, mice in each group were given the drug (1.0, 10.0, 30.0 mg/kg) intragastric stimulation and mouse hippocampal tissues were taken to perform iTRAQ to identify differentially expressed proteins, and bioinformatics was used to analyze the functional enrichment of the differentially expressed proteins. Compared with Ctr group, the number of differentially expressed proteins in HNK, I5, and I6 treatment groups was 158, 88, and 105, respectively. The three groups shared 29 differentially expressed proteins. In addition, compared with HNK group, the number of differentially expressed proteins in I5 and I6 groups was 201 and 203, respectively. A total of 47 and 56 differentially expressed proteins were co-expressed in I5 and I6 groups. Bioinformatics analysis showed that these differentially expressed proteins mainly had the functions of binding, biocatalysis, and transport, and mainly participated in cellular process, biological regulation process, biological metabolism process, and stress reaction process. GO and KEGG pathway analysis found that these differentially expressed proteins were involved long-term potentiation, G13 pathway, platelet activation pathway, and MAPK signaling pathway. HNK, I5, and I6 antidepressants are closely related to sudden stress sensitivity, stress resistance, neurotransmitter, and metabolic pathways. This study provides a scientific basis to further elucidate the mechanism and clinical application of HNK, I5, and I6 antidepressants.

Indexed as

KetamineProteomicsAnimalsAntidepressive AgentsMiceSignal Transduction6-hydroxynorketamineAntidepressive AgentsKetamineAnti-depressionHippocampusHNKiTRAQProteomics

Identifiers

PMID37632679
OpenAlexW4386187190

What OpenQuestion holds

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Registered trials

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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.