Evidence map›Paper›PMID 39283715›Full record

ArticleThe international journal of neuropsychopharmacology2024

Upregulation of Phosphodiesterase 7A Contributes to Concurrent Pain and Depression via Inhibition of cAMP-PKA-CREB-BDNF Signaling and Neuroinflammation in the Hippocampus of Mice.

Shi-Cai Chen, Yan-Han Chen, Yan Song, Shu-Hua Zong, Ming-Xia Wu, Wei Wang, Hao Wang, Feng Zhang, Yan-Meng Zhou, Hai-Yang Yu and 2 more

Abstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Molecular medicine reports · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

12 authors.

Shi-Cai ChenInstitute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Ji'nan, China.
Yan-Han ChenInstitute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Ji'nan, China.
Yan SongDepartment of Pharmacy, Taian Maternal and Child Health Hospital, Tai'an, China.
Shu-Hua ZongInstitute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Ji'nan, China.
Ming-Xia WuInstitute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Ji'nan, China.
Wei WangInstitute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Ji'nan, China.
Hao WangInstitute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Ji'nan, China.
Feng ZhangInstitute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Ji'nan, China.
Yan-Meng ZhouInstitute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Ji'nan, China.
Hai-Yang YuInstitute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Ji'nan, China.
Han-Ting ZhangInstitute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Ji'nan, China.
Fang-Fang ZhangDepartment of Pharmacology, School of Pharmacy, Qingdao University, Qingdao, China.ORCID 0000-0002-9348-7596

Funding

National Natural Science Foundation of China 81773717Shandong Provincial Natural Science foundation ZR2023MH119
6 · The paper itself

Abstract

backgroundPhosphodiesterases (PDEs) are enzymes that catalyze the hydrolysis of cyclic adenosine monophosphate AMP (cAMP) and/or cyclic guanosine monophosphate (cGMP). PDE inhibitors can mitigate chronic pain and depression when these disorders occur individually; however, there is limited understanding of their role in concurrent chronic pain and depression. We aimed to evaluate the mechanisms of action of PDE using 2 mouse models of concurrent chronic pain and depression.

methodsC57BL/6J mice were subjected to partial sciatic nerve ligation (PSNL) to induce chronic neuropathic pain or injected with complete Freund's adjuvant (CFA) to induce inflammatory pain, and both animals showed depression-like behavior. First, we determined the change in PDE expression in both animal models. Next, we determined the effect of PDE7 inhibitor BRL50481 or hippocampal PDE7A knockdown on PSNL- or CFA-induced chronic pain and depression-like behavior. We also investigated the role of cAMP-protein kinase A (PKA)-cAMP response element binding protein (CREB)-brain-derived neurotrophic factor (BDNF) signaling and neuroinflammation in the effect of PDE7A inhibition on PSNL- or CFA-induced chronic pain and depression-like behavior.

resultsThis induction of chronic pain and depression in the 2 animal models upregulated hippocampal PDE7A. Oral administration of PDE7 inhibitor, BRL50481, or hippocampal PDE7A knockdown significantly reduced mechanical hypersensitivity and depression-like behavior. Hippocampal PDE7 inhibition reversed PSNL- or CFA-induced downregulation of cAMP and BDNF and the phosphorylation of PKA, CREB, and p65. cAMP agonist forskolin reversed these changes and caused milder behavioral symptoms of pain and depression. BRL50481 reversed neuroinflammation in the hippocampus in PSNL mice.

conclusionsHippocampal PDE7A mediated concurrent chronic pain and depression in both mouse models by inhibiting cAMP-PKA-CREB-BDNF signaling. Inhibiting PDE7A or activating cAMP-PKA-CREB-BDNF signaling are potential strategies to treat concurrent chronic pain and depression.

Indexed as

Brain-Derived Neurotrophic FactorChronic PainCyclic AMPCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteinCyclic Nucleotide Phosphodiesterases, Type 7DepressionHippocampusMice, Inbred C57BLSignal TransductionUp-RegulationAnimalsDisease Models, AnimalImidazolesMaleMice2-(3,4-dimethoxybenzyl)-7-(1-(1-hydroxyethyl)-4-phenylbutyl)-5-methylimidazo(5,1-f)(1,2,4)triazin-4 (3H)-oneBdnf protein, mouseBrain-Derived Neurotrophic FactorCreb1 protein, mouseCyclic AMPCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteinCyclic Nucleotide Phosphodiesterases, Type 7ImidazolesPde7a protein, mousePhosphodiesterase InhibitorsTriazinesChronic paincyclic adenosine monophosphatedepressionneuroinflammationphosphodiesterase7A

Identifiers

PMID39283715
PMCPMC11487153

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.