Evidence map›Paper›PMID 29704309›Full record

ArticleCNS neuroscience & therapeutics2018

The neuroprotective and antidepressant-like effects of Hcyb1, a novel selective PDE2 inhibitor.

Li Liu, Jing Zheng, Xian-Feng Huang, Xia Zhu, Shu-Ming Ding, Heng-Ming Ke, James M O'Donnell, Han-Ting Zhang, Guo-Qiang Song, Ying Xu

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  9. GW117: A novel serotonin (5-HTCNS neuroscience & therapeutics · 2021
    Article
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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

10 authors at 5 institutions in 2 countries.

Li LiuSchool of Pharmaceutical Engineering and Life Sciences, Changzhou University, Changzhou, China.
Jing ZhengSchool of Pharmaceutical Engineering and Life Sciences, Changzhou University, Changzhou, China.
Xian-Feng HuangSchool of Pharmaceutical Engineering and Life Sciences, Changzhou University, Changzhou, China.
Xia ZhuDepartment of Pharmacology, School of Pharmacy, Xuzhou Medical University, Xuzhou, China.
Shu-Ming DingSchool of Pharmaceutical Engineering and Life Sciences, Changzhou University, Changzhou, China.
Heng-Ming KeDepartment of Biochemistry and Biophysics and Lineberger Comprehensive Cancer Center, The University of North Carolina, Chapel Hill, NC, USA.
James M O'DonnellDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, NY, USA.
Han-Ting ZhangDepartment of Behavioral Medicine & Psychiatry and Physiology, Pharmacology & Neuroscience, Rockefeller Neurosciences Institute, West Virginia University Health Science Center, Morgantown, WV, USA.
Guo-Qiang SongSchool of Pharmaceutical Engineering and Life Sciences, Changzhou University, Changzhou, China.
Ying XuDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, NY, USA.ORCID 0000-0001-5479-7922
Changzhou University · CNUniversity at Buffalo, State University of New York · USUniversity of North Carolina at Chapel Hill · USWest Virginia University · USXuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsDepression is currently the most common mood disorder. Regulation of intracellular cyclic adenosine monophosphate (cAMP) and/or cyclic guanosine monophosphate (cGMP) signaling by phosphodiesterase (PDE) inhibition has been paid much attention for treatment of depression. This study aimed to investigate the neuroprotective effects of Hcyb1, a novel PDE2 inhibitor, in HT-22 cells and antidepressant-like effects in mouse models of depression.

methodsHcyb1 was synthesized and its selectivity upon PDE2 was tested. Moreover, HT-22 hippocampal cells were used to determine the effects of Hcyb1 on cell viability, cyclic nucleotide levels, and the downstream molecules related to cAMP/cGMP signaling by neurochemical, enzyme-linked immunosorbent, and immunoblot assays in vitro. The antidepressant-like effects of Hcyb1 were also determined in the forced swimming and tail suspension tests in mice.

resultsHcyb1 had a highly selective inhibition of PDE2A (IC

conclusionThese results suggest that the novel PDE2 inhibitor Hcyb1 produced neuroprotective and antidepressant-like effects most likely mediated by cAMP/cGMP-CREB-BDNF signaling.

Indexed as

AnimalsAntidepressive AgentsBrain-Derived Neurotrophic FactorCell Line, TransformedCREB-Binding ProteinCyclic AMPCyclic GMPDepressionDisease Models, AnimalGuanineHindlimb SuspensionInhibitory Concentration 50LocomotionMaleMiceMice, Inbred ICRAntidepressive AgentsBrain-Derived Neurotrophic FactorCREB-Binding ProteinCyclic AMPCyclic GMPGuanineNaphthalenesNeuroprotective AgentsN-MethylaspartatePDE2 inhibitor hcyb1Phosphodiesterase Inhibitorsantidepressantcell viabilitycyclic nucleotideforced swim testHcyb1phosphodiesterase 2(PDE2) inhibitortail suspension test

Identifiers

PMID29704309
PMCPMC6489804
OpenAlexW2799853688

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.