Evidence map›Paper›PMID 27483126›Full record

ArticleAnesthesiology2016

Contribution of the Suppressor of Variegation 3-9 Homolog 1 in Dorsal Root Ganglia and Spinal Cord Dorsal Horn to Nerve Injury-induced Nociceptive Hypersensitivity.

Jun Zhang, Lingli Liang, Xuerong Miao, Shaogen Wu, Jing Cao, Bo Tao, Qingxiang Mao, Kai Mo, Ming Xiong, Brianna Marie Lutz and 2 more

Open access · greenAbstract read
In one paragraph

Article in Anesthesiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

  1. The Role of Methylation Modification in Neural Injury and Repair.International journal of molecular sciences · 2025
    Review
  2. Article
  3. Review
  4. The Downregulation of Opioid Receptors and Neuropathic Pain.International journal of molecular sciences · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. CREB Participates in Paclitaxel-Induced Neuropathic Pain Genesis Through Transcriptional Activation of Dnmt3a in Primary Sensory Neurons.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Article
  10. Article
  11. NAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
  12. Article
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  14. DNMT3a-triggered downregulation of KInternational journal of cancer · 2019
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  16. TET1 Overexpression Mitigates Neuropathic Pain Through Rescuing the Expression of μ-Opioid Receptor and Kv1.2 in the Primary Sensory Neurons.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2019
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 2 countries.

Jun ZhangFrom the Department of Anesthesiology, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, New Jersey (J.Z., L.L., X.M., S.W., J.C., Q.M., K.M., M.X., B.M.L., A.B., Y.-X.T.); Department of Anesthesiology, Union Medical Center, Nankai University, Tianjin, China (J.Z.); Department of Anesthesiology and Intensive Care, Eastern Hepatobiliary Surgical Hospital, The Second Military Medical University, Shanghai, China (X.M.); Rowan University School of Osteopathic Medicine, Stratford, New Jersey (B.T.); Department of Anesthesiology, Institute of Surgery Research, Daping Hospital, The Third Military Medical University, Chongqing, China (Q.M.); and Departments of Cell Biology and Molecular Medicine (Y.-X.T.) and Physiology, Pharmacology and Neuroscience (Y.-X.T.), New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, New Jersey.
Lingli Liang
Xuerong Miao
Shaogen Wu
Jing Cao
Bo Tao
Qingxiang Mao
Kai Mo
Ming Xiong
Brianna Marie Lutz
Alex Bekker
Yuan-Xiang Tao
Rutgers, The State University of New Jersey · USNankai University · CN

Funding

The Role of Endothelin-1 in Sickle Cell DiseaseU01HL117684 · NHLBI · AUGUSTA UNIVERSITY · PI KUTLAR, ABDULLAH, MEILER, STEFFEN · 2013 to 2017
$8.1M
Epigenetic regulation of neuropathic pain: Role of DRG histone methyltransferase G9aR01NS094664 · NINDS · RBHS-NEW JERSEY MEDICAL SCHOOL · PI TAO, YUAN-XIANG · 2016 to 2020
$2.0M
mTOR, a new target for opioid-induced tolerance and hyperalgesiaR01DA033390 · NIDA · RBHS-NEW JERSEY MEDICAL SCHOOL · PI TAO, YUAN-XIANG · 2013 to 2017
$1.8M
Epigenetic Regulation of Neuropathic Pain: Role of Native Kv1.2 Antisense RNAR01NS072206 · NINDS · RBHS-NEW JERSEY MEDICAL SCHOOL · PI TAO, YUAN-XIANG · 2011 to 2014
$1.4M
Epigenetic mechanism of nerve injury-induced Kv1.2 downregulation in DRG neuronsF31NS092310 · NINDS · RBHS-NEW JERSEY MEDICAL SCHOOL · PI LUTZ, BRIANNA M. · 2015 to 2017
$89k
NHLBI NIH HHS U01 HL117684NIDA NIH HHS R01 DA033390NINDS NIH HHS F31 NS092310NINDS NIH HHS R01 NS072206NINDS NIH HHS R01 NS094664
6 · The paper itself

Abstract

backgroundPeripheral nerve injury-induced gene alterations in the dorsal root ganglion (DRG) and spinal cord likely participate in neuropathic pain genesis. Histone methylation gates gene expression. Whether the suppressor of variegation 3-9 homolog 1 (SUV39H1), a histone methyltransferase, contributes to nerve injury-induced nociceptive hypersensitivity is unknown.

methodsQuantitative real-time reverse transcription polymerase chain reaction analysis, Western blot analysis, or immunohistochemistry were carried out to examine the expression of SUV39H1 mRNA and protein in rat DRG and dorsal horn and its colocalization with DRG μ-opioid receptor (MOR). The effects of a SUV39H1 inhibitor (chaetocin) or SUV39H1 siRNA on fifth lumbar spinal nerve ligation (SNL)-induced DRG MOR down-regulation and nociceptive hypersensitivity were examined.

resultsSUV39H1 was detected in neuronal nuclei of the DRG and dorsal horn. It was distributed predominantly in small DRG neurons, in which it coexpressed with MOR. The level of SUV39H1 protein in both injured DRG and ipsilateral fifth lumbar dorsal horn was time dependently increased after SNL. SNL also produced an increase in the amount of SUV39H1 mRNA in the injured DRG (n = 6/time point). Intrathecal chaetocin or SUV39H1 siRNA as well as DRG or intraspinal microinjection of SUV39H1 siRNA impaired SNL-induced allodynia and hyperalgesia (n = 5/group/treatment). DRG microinjection of SUV39H1 siRNA also restored SNL-induced DRG MOR down-regulation (n = 6/group).

conclusionsThe findings of this study suggest that SUV39H1 contributes to nerve injury-induced allodynia and hyperalgesia through gating MOR expression in the injured DRG. SUV39H1 may be a potential target for the therapeutic treatment of nerve injury-induced nociceptive hypersensitivity.

Indexed as

AnimalsBlotting, WesternDisease Models, AnimalDown-RegulationGanglia, SpinalHyperalgesiaImmunohistochemistryMaleMethyltransferasesNeuralgiaPeripheral Nerve InjuriesRatsRats, Sprague-DawleyRepressor ProteinsReverse Transcriptase Polymerase Chain ReactionSpinal Cord Dorsal HornMethyltransferasesRepressor ProteinsSuv39h1 protein, rat

Identifiers

PMID27483126
PMCPMC5030174
OpenAlexW2514699001

What OpenQuestion holds

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LicenceTDM
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.