Evidence map›Paper›PMID 34093390›Full record

ArticleFrontiers in neurology2021

Behavioral and Histopathological Impairments Caused by Topical Exposure of the Rat Brain to Mild-Impulse Laser-Induced Shock Waves: Impulse Dependency.

Motoyuki Jitsu, Katsuki Niwa, Go Suzuki, Takeyuki Obara, Yukiko Iwama, Kohsuke Hagisawa, Yukihiro Takahashi, Yoshitaro Matsushita, Satoru Takeuchi, Hiroshi Nawashiro and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
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 at 2 institutions in 1 country.

Motoyuki JitsuMilitary Medicine Research Unit, Japan Ground Self Defense Force, Tokyo, Japan.
Katsuki NiwaMilitary Medicine Research Unit, Japan Ground Self Defense Force, Tokyo, Japan.
Go SuzukiMilitary Medicine Research Unit, Japan Ground Self Defense Force, Tokyo, Japan.
Takeyuki ObaraMilitary Medicine Research Unit, Japan Ground Self Defense Force, Tokyo, Japan.
Yukiko IwamaMilitary Medicine Research Unit, Japan Ground Self Defense Force, Tokyo, Japan.
Kohsuke HagisawaMilitary Medicine Research Unit, Japan Ground Self Defense Force, Tokyo, Japan.
Yukihiro TakahashiMilitary Medicine Research Unit, Japan Ground Self Defense Force, Tokyo, Japan.
Yoshitaro MatsushitaMilitary Medicine Research Unit, Japan Ground Self Defense Force, Tokyo, Japan.
Satoru TakeuchiDepartment of Neurosurgery, National Defense Medical College, Tokorozawa, Japan.
Hiroshi NawashiroDepartment of Neurosurgery, National Defense Medical College, Tokorozawa, Japan.
Shunichi SatoDivision of Bioinformation and Therapeutic Systems, National Defense Medical College Research Institute, Tokorozawa, Japan.
Satoko KawauchiDivision of Bioinformation and Therapeutic Systems, National Defense Medical College Research Institute, Tokorozawa, Japan.
Self-Defense Forces Central Hospital · JPNational Defense Medical College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although an enormous number of animal studies on blast-induced traumatic brain injury (bTBI) have been conducted, there still remain many uncertain issues in its neuropathology and mechanisms. This is partially due to the complex and hence difficult experimental environment settings, e.g., to minimize the effects of blast winds (tertiary mechanism) and to separate the effects of brain exposure and torso exposure. Since a laser-induced shock wave (LISW) is free from dynamic pressure and its energy is spatially well confined, the effects of pure shock wave exposure (primary mechanism) solely on the brain can be examined by using an LISW. In this study, we applied a set of four LISWs in the impulse range of 15-71 Pa·s to the rat brain through the intact scalp and skull; the interval between each exposure was ~5 s. For the rats, we conducted locomotor activity, elevated plus maze and forced swimming tests. Axonal injury in the brain was also examined by histological analysis using Bodian silver staining. Only the rats with exposure at higher impulses of 54 and 71 Pa·s showed significantly lower spontaneous movements at 1 and 2 days post-exposure by the locomotor activity test, but after 3 days post-exposure, they had recovered. At 7 days post-exposure, however, these rats (54 and 71 Pa·s) showed significantly higher levels of anxiety-related and depression-like behaviors by the elevated plus maze test and forced swimming test, respectively. To the best of the authors' knowledge, there have been few studies in which a rat model showed both anxiety-related and depression-like behaviors caused by blast or shock wave exposure. At that time point (7 days post-exposure), histological analysis showed significant decreases in axonal density in the cingulum bundle and corpus callosum in impulse-dependent manners; axons in the cingulum bundle were found to be more affected by a shock wave. Correlation analysis showed a statistically significant correlation between the depression like-behavior and axonal density reduction in the cingulum bundle. The results demonstrated the dependence of behavior deficits and axonal injury on the shock wave impulse loaded on the brain.

Indexed as

blast-induced traumatic brain injurydiffuse axonal injuryelevated plus maze testforced swimming testlaser-induced shock wavespontaneous motor activity

Identifiers

PMID34093390
PMCPMC8177106
OpenAlexW3163130951

What OpenQuestion holds

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LicenceCC BY
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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.