Evidence map›Paper›PMID 27406816›Full record

ArticleNeurocritical care2017

Simvastatin Therapy in the Acute Stage of Traumatic Brain Injury Attenuates Brain Trauma-Induced Depression-Like Behavior in Rats by Reducing Neuroinflammation in the Hippocampus.

Sher-Wei Lim, Yow-Ling Shiue, Jen-Chieh Liao, Hsiao-Yue Wee, Che-Chuan Wang, Chung-Ching Chio, Chin-Hung Chang, Chiao-Ya Hu, Jinn-Rung Kuo

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In one paragraph

Article in Neurocritical care, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 64 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Sher-Wei LimInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan.
Yow-Ling ShiueInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan.
Jen-Chieh LiaoDepartments of Neurosurgery, Chi-Mei Medical Center, Tainan, Taiwan.
Hsiao-Yue WeeDepartment of Neurosurgery, Chi-Mei Medical Center, Liouying, Tainan, Taiwan.
Che-Chuan WangDepartments of Neurosurgery, Chi-Mei Medical Center, Tainan, Taiwan.
Chung-Ching ChioDepartments of Neurosurgery, Chi-Mei Medical Center, Tainan, Taiwan.
Chin-Hung ChangDepartments of Neurosurgery, Chi-Mei Medical Center, Tainan, Taiwan.
Chiao-Ya HuDepartment of Medical Research, Chi-Mei Medical Center, Tainan, Taiwan.
Jinn-Rung KuoDepartments of Neurosurgery, Chi-Mei Medical Center, Tainan, Taiwan. kuojinnrung@gmail.com.
Chi Mei Medical Center · TWSouthern Taiwan University of Science and Technology · TWNational Sun Yat-sen University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe antidepressant-like effects of simvastatin on traumatic brain injury (TBI) remain unclear. The present study aimed to investigate the neuroprotective effects of simvastatin and determine whether simvastatin attenuates TBI-induced depression-like behavior and, more specifically, acts as an antineuroinflammatory.

methodsAnesthetized male Sprague-Dawley rats were divided into five groups: sham-operated controls, TBI controls, and TBI treatment with simvastatin 4, 10, or 20 mg/kg. Simvastatin was intraperitoneally injected 0, 24, and 48 h after TBI. The motor function was measured using an inclined plane, and depression-like behavior was evaluated using forced swimming tests. Neuronal apoptosis (markers: NeuN, TUNEL, caspase-3), microglia (marker: OX42) and astrocyte (marker: GFAP) activation, and TNF-α expression in the microglia and astrocytes of the hippocampal CA3 area were investigated using immunofluorescence assay. All parameters were measured on the 4th, 8th, and 15th day, or only on the 15th day after TBI.

resultsTBI-induced depression-like behavior, which increased duration of immobility, was significantly attenuated by 20 mg simvastatin therapy on day 15 after TBI. TBI-induced neuronal apoptosis, microglia and astrocyte activation, and TNF-α expression in the microglia and astrocytes of the CA3 area of the hippocampus were significantly reduced by simvastatin treatment, particularly when 20 mg/kg was administered for 3 days.

conclusionsIntraperitoneal injection of simvastatin attenuated TBI in rats during the acute stage by reducing neuronal apoptosis, microglia, and TNF-α expression, thereby resulting in a reduction of depressive-like behavior. Our results suggest that simvastatin may be a promising treatment for TBI-induced depression-like behavior.

Indexed as

Acute DiseaseAnimalsBehavior, AnimalBrain Injuries, TraumaticDepressionDisease Models, AnimalHippocampusHydroxymethylglutaryl-CoA Reductase InhibitorsInflammationInjections, IntraperitonealMaleRatsRats, Sprague-DawleySimvastatinHydroxymethylglutaryl-CoA Reductase InhibitorsSimvastatinDepression-like behaviorFluid percussion injuryForced swimHippocampusMaximal angleMicrogliaSimvastatinTumor necrosis factor-alpha

Identifiers

PMID27406816
OpenAlexW2468108921

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.