Evidence map›Paper›PMID 27852966›Full record

ArticleMolecular pain2016

Hippocampal activation of microglia may underlie the shared neurobiology of comorbid posttraumatic stress disorder and chronic pain.

Rao Sun, Zuoxia Zhang, Yishan Lei, Yue Liu, Cui'e Lu, Hui Rong, Yu'e Sun, Wei Zhang, Zhengliang Ma, Xiaoping Gu

Open access · goldAbstract read
In one paragraph

Article in Molecular pain, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

35 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
  2. Sex-specific role of microglia in ΔNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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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 1 institution in 1 country.

Rao SunDepartment of Anesthesiology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Zuoxia ZhangDepartment of Anesthesiology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Yishan LeiDepartment of Anesthesiology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Yue LiuDepartment of Anesthesiology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Cui'e LuDepartment of Anesthesiology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Hui RongDepartment of Anesthesiology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Yu'e SunDepartment of Anesthesiology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Wei ZhangDepartment of Anesthesiology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Zhengliang MaDepartment of Anesthesiology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China mazhengliang1964@nju.edu.cn xiaopinggu@nju.edu.cn.
Xiaoping GuDepartment of Anesthesiology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Nanjing Drum Tower Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The high comorbidity rates of posttraumatic stress disorder and chronic pain have been widely reported, but the underlying mechanisms remain unclear. Emerging evidence suggested that an excess of inflammatory immune activities in the hippocampus involved in the progression of both posttraumatic stress disorder and chronic pain. Considering that microglia are substrates underlying the initiation and propagation of the neuroimmune response, we hypothesized that stress-induced activation of hippocampal microglia may contribute to the pathogenesis of posttraumatic stress disorder-pain comorbidity. We showed that rats exposed to single prolonged stress, an established posttraumatic stress disorder model, exhibited persistent mechanical allodynia and anxiety-like behavior, which were accompanied by increased activation of microglia and secretion of pro-inflammatory cytokines in the hippocampus. Correlation analyses showed that hippocampal activation of microglia was significantly correlated with mechanical allodynia and anxiety-like behavior. Our data also showed that both intraperitoneal and intra-hippocampal injection of minocycline suppressed single prolonged stress-induced microglia activation and inflammatory cytokines accumulation in the hippocampus, and attenuated both single prolonged stress-induced mechanical allodynia and anxiety-like behavior. Taken together, the present study suggests that stress-induced microglia activation in the hippocampus may serve as a critical mechanistic link in the comorbid relationship between posttraumatic stress disorder and chronic pain. The novel concept introduces the possibility of cotreating chronic pain and posttraumatic stress disorder.

Indexed as

Chronic PainHippocampusMicrogliaStress Disorders, Post-TraumaticAnimalsBehavior, AnimalCytokinesDisease Models, AnimalHyperalgesiaMaleMinocyclineRats, Sprague-DawleyStress, PhysiologicalCytokinesMinocyclinechronic paincomorbidityhippocampusmicrogliaPosttraumatic stress disorderstress-induced hyperalgesia

Identifiers

PMID27852966
PMCPMC5117253
OpenAlexW2552312039

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.