Evidence map›Paper›PMID 27791037›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Orthopedic surgery modulates neuropeptides and BDNF expression at the spinal and hippocampal levels.

Ming-Dong Zhang, Swapnali Barde, Ting Yang, Beilei Lei, Lars I Eriksson, Joseph P Mathew, Thomas Andreska, Katerina Akassoglou, Tibor Harkany, Tomas G M Hökfelt and 1 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

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  17. Fracture-induced pain-like behaviours in a femoral fracture mouse model.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 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

11 authors at 6 institutions in 4 countries.

Ming-Dong ZhangDepartment of Neuroscience, Karolinska Institutet, Stockholm 171 77, Sweden; mingdong.zhang@ki.se tomas.hokfelt@ki.se niccolo.terrando@duke.edu.
Swapnali BardeDepartment of Neuroscience, Karolinska Institutet, Stockholm 171 77, Sweden.
Ting YangDepartment of Physiology and Pharmacology, Section for Anesthesiology and Intensive Care Medicine, Karolinska Institutet, Stockholm 171 77, Sweden; Division of Nephrology, Department of Medicine, Duke University Medical Center, Durham, NC 27710.
Beilei LeiDepartment of Anesthesiology, Duke University Medical Center, Durham, NC 27710.
Lars I ErikssonDepartment of Physiology and Pharmacology, Section for Anesthesiology and Intensive Care Medicine, Karolinska Institutet, Stockholm 171 77, Sweden; Function Perioperative Medicine and Intensive Care, Karolinska University Hospital, Stockholm 171 76, Sweden.
Joseph P MathewDepartment of Anesthesiology, Duke University Medical Center, Durham, NC 27710.
Thomas AndreskaInstitute of Clinical Neurobiology, University of Würzburg, 97078 Wuerzburg, Germany.
Katerina AkassoglouGladstone Institute of Neurological Disease, University of California, San Francisco, CA 94158; Department of Neurology, University of California, San Francisco, CA 94158.
Tibor HarkanyDepartment of Neuroscience, Karolinska Institutet, Stockholm 171 77, Sweden; Department of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, A-1090 Vienna, Austria.
Tomas G M HökfeltDepartment of Neuroscience, Karolinska Institutet, Stockholm 171 77, Sweden; mingdong.zhang@ki.se tomas.hokfelt@ki.se niccolo.terrando@duke.edu.
Niccolò TerrandoDepartment of Physiology and Pharmacology, Section for Anesthesiology and Intensive Care Medicine, Karolinska Institutet, Stockholm 171 77, Sweden; Department of Anesthesiology, Duke University Medical Center, Durham, NC 27710; mingdong.zhang@ki.se tomas.hokfelt@ki.se niccolo.terrando@duke.edu.
Karolinska Institutet · SEDuke Medical Center · USKarolinska University Hospital · SEMedical University of Vienna · ATUniversity of California, San Francisco · USUniversity of Würzburg · DE

Funding

Mechanisms of Fibrin Action in Multiple SclerosisR01NS052189 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI AKASSOGLOU, KATERINA · 2005 to 2016
$5.1M
Mechanisms and functions of p75 neurotrophin receptor signaling in astrocytesR01NS051470 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI AKASSOGLOU, KATERINA · 2005 to 2015
$4.0M
Mechanisms of Fibrin Action in Neuronal FunctionsR21NS082976 · NINDS · J. DAVID GLADSTONE INSTITUTES · PI AKASSOGLOU, KATERINA · 2014 to 2015
$525k
NINDS NIH HHS R01 NS051470NINDS NIH HHS R01 NS052189NINDS NIH HHS R21 NS082976
6 · The paper itself

Abstract

Pain is a critical component hindering recovery and regaining of function after surgery, particularly in the elderly. Understanding the role of pain signaling after surgery may lead to novel interventions for common complications such as delirium and postoperative cognitive dysfunction. Using a model of tibial fracture with intramedullary pinning in male mice, associated with cognitive deficits, we characterized the effects on the primary somatosensory system. Here we show that tibial fracture with pinning triggers cold allodynia and up-regulates nerve injury and inflammatory markers in dorsal root ganglia (DRGs) and spinal cord up to 2 wk after intervention. At 72 h after surgery, there is an increase in activating transcription factor 3 (ATF3), the neuropeptides galanin and neuropeptide Y (NPY), brain-derived neurotrophic factor (BDNF), as well as neuroinflammatory markers including ionized calcium-binding adaptor molecule 1 (Iba1), glial fibrillary acidic protein (GFAP), and the fractalkine receptor CX3CR1 in DRGs. Using an established model of complete transection of the sciatic nerve for comparison, we observed similar but more pronounced changes in these markers. However, protein levels of BDNF remained elevated for a longer period after fracture. In the hippocampus, BDNF protein levels were increased, yet there were no changes in Bdnf mRNA in the parent granule cell bodies. Further, c-Fos was down-regulated in the hippocampus, together with a reduction in neurogenesis in the subgranular zone. Taken together, our results suggest that attenuated BDNF release and signaling in the dentate gyrus may account for cognitive and mental deficits sometimes observed after surgery.

Indexed as

Activating Transcription Factor 3AnimalsBrain-Derived Neurotrophic FactorCalcium-Binding ProteinsCognitive DysfunctionCX3C Chemokine Receptor 1Dentate GyrusFracture Fixation, IntramedullaryGalaninGanglia, SpinalGene Expression RegulationGlial Fibrillary Acidic ProteinHyperalgesiaMaleMiceMice, Inbred C57BLActivating Transcription Factor 3Aif1 protein, mouseAtf3 protein, mouseBrain-Derived Neurotrophic FactorCalcium-Binding ProteinsCX3C Chemokine Receptor 1Cx3cr1 protein, mouseGalaninGlial Fibrillary Acidic ProteinMicrofilament ProteinsNeuropeptide YProto-Oncogene Proteins c-fosdeliriummemorynerve injuryneurogenesispostoperative pain

Identifiers

PMID27791037
PMCPMC5086993
OpenAlexW2531309662

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.