Evidence map›Paper›PMID 36092814›Full record

ArticleFrontiers in aging neuroscience2022

Brain region-specific microglial and astrocytic activation in response to systemic lipopolysaccharides exposure.

Edoardo Brandi, Laura Torres-Garcia, Alexander Svanbergsson, Caroline Haikal, Di Liu, Wen Li, Jia-Yi Li

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2022. 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
3.9field-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, 38 citations in OpenAlex.

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  12. Bradykinin Type 2 Receptor Deficiency Reshapes Acute Neuroinflammation and Improves Cell Survival after Ischemic Stroke in Diabetic Mice.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
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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

7 authors at 2 institutions in 2 countries.

Edoardo BrandiNeural Plasticity and Repair Unit, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Laura Torres-GarciaNeural Plasticity and Repair Unit, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Alexander SvanbergssonNeural Plasticity and Repair Unit, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Caroline HaikalNeural Plasticity and Repair Unit, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Di LiuHealth Sciences Institute, China Medical University, Shenyang, China.
Wen LiNeural Plasticity and Repair Unit, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Jia-Yi LiNeural Plasticity and Repair Unit, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Lund University · SEChina Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglia cells are the macrophage population within the central nervous system, which acts as the first line of the immune defense. These cells present a high level of heterogeneity among different brain regions regarding morphology, cell density, transcriptomes, and expression of different inflammatory mediators. This region-specific heterogeneity may lead to different neuroinflammatory responses, influencing the regional involvement in several neurodegenerative diseases. In this study, we aimed to evaluate microglial response in 16 brain regions. We compared different aspects of the microglial response, such as the extension of their morphological changes, sensitivity, and ability to convert an acute inflammatory response to a chronic one. Then, we investigated the synaptic alterations followed by acute and chronic inflammation in substantia nigra. Moreover, we estimated the effect of partial ablation of fractalkine CX3C receptor 1 (CX3CR1) on microglial response. In the end, we briefly investigated astrocytic heterogeneity and activation. To evaluate microglial response in different brain regions and under the same stimulus, we induced a systemic inflammatory reaction through a single intraperitoneal (i.p.) injection of lipopolysaccharides (LPS). We performed our study using C57BL6 and CX3CR1

Indexed as

astrocyteCX3CR1dopaminergic (DA) neuronlipopolysaccharide (LPS)microglianeuroinflammationsubstantia nigra (SN)

Identifiers

PMID36092814
PMCPMC9459169
OpenAlexW4293194600

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.