Evidence map›Paper›PMID 31949570›Full record

ArticleInternational journal of clinical and experimental pathology2018

LPS induces dopamine depletion and iron accumulation in substantia nigra in rat models of Parkinson's disease.

Jie Huo, Qu Cui, Wei Yang, Wei Guo

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Ferroptosis Mechanisms Involved in Hippocampal-Related Diseases.International journal of molecular sciences · 2021
    Review
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

4 authors at 2 institutions in 1 country.

Jie HuoDepartment of Emergency, Beijing Tiantan Hospital, Capital Medical University Beijing, China.
Qu CuiDepartment of Emergency, Beijing Tiantan Hospital, Capital Medical University Beijing, China.
Wei YangDepartment of Immunology, School of Basic Medicine, Norman Bethune Health Science Center, Jilin University Jilin, China.
Wei GuoDepartment of Emergency, Beijing Tiantan Hospital, Capital Medical University Beijing, China.
Beijing Tian Tan Hospital · CNFirst Bethune Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIntrapallidal inflammation may lead to the pathogenesis of Parkinson's disease. Pathological changes caused by lipopolysaccharide (LPS)-induced inflammation in Parkinson's disease rat models were largely unknown.

methodsMale Sprague-Dawley rat models were intra-globuspallidus injected with saline and lipopolysaccharide and divided into two groups, the control group and the LPS-stimulation group. The locomotor activity of the rat models was recorded for 4 consecutive weeks by trajectory analysis software for animal behavior. For the evaluation of pathological profiles, the expression levels of tyrosine hydroxylase and OX-42 in the substantia nigra tissues were detected by immunohistochemical staining. Also, the concentrations of dopamine at specific sites were detected through high-performance liquid chromatography. Perl's iron staining was used to evaluate iron accumulation in substantia nigra tissues.

resultsLPS-stimulation reduced the locomotor capacity of the rat models compared with the control group. The density of tyrosine hydroxylase-positive cells was reduced and the secretion of striatal dopamine in the substantia nigra pars compacts was lower in the LPS group than it was in the control group. OX-42 positive microglia and ferritin levels were enhanced in the LPS group.

conclusionIntrapallidal inflammation by LPS induced dopamine depletion and iron accumulation in the substantia nigra of Parkinson's disease rat models. The management of cerebral inflammation might be pivotal for PD pathogenesis and prognosis.

Indexed as

inflammationironlipopolysaccharideParkinson disease

Identifiers

PMID31949570
PMCPMC6962913
OpenAlexW3010537490

What OpenQuestion holds

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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.