Evidence map›Paper›PMID 31055628›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2019

Ligustroflavone reduces necroptosis in rat brain after ischemic stroke through targeting RIPK1/RIPK3/MLKL pathway.

Yi-Yue Zhang, Wei-Ning Liu, Yue-Qi Li, Xiao-Jie Zhang, Jie Yang, Xiu-Ju Luo, Jun Peng

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In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 9% 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, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

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  20. Progress in study on the final executor of necroptosis MLKL and its inhibitors.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
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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 3 institutions in 1 country.

Yi-Yue ZhangDepartment of Pharmacology, Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410078, China.
Wei-Ning LiuDepartment of Pharmacology, Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410078, China.
Yue-Qi LiDepartment of Laboratory Medicine, The Third Xiangya Hospital of Central South University, Changsha, 410013, China.
Xiao-Jie ZhangDepartment of Pharmacology, Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410078, China.
Jie YangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Xiu-Ju LuoDepartment of Laboratory Medicine, The Third Xiangya Hospital of Central South University, Changsha, 410013, China. xjluo22@csu.edu.cn.
Jun PengDepartment of Pharmacology, Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410078, China. Junpeng@csu.edu.cn.
Central South University · CNThird Xiangya Hospital · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Receptor-interacting protein kinase 1/3 (RIPK1/3) and mixed lineage kinase domain-like (MLKL)-mediated necroptosis contributes to brain injury after ischemic stroke. Ligustroflavone is an ingredient of common privet with activities of anti-inflammation and complement inhibition. This study aims to explore the effect of ligustroflavone on ischemic brain injury in stroke rat and the underlying mechanisms. A rat model of ischemic stroke was established by middle cerebral artery occlusion (MCAO), which showed ischemic injury (increase in neurological deficit score and infarct volume) and upregulation of necroptosis-associated proteins (RIPK1, RIPK3 and MLKL/p-MLKL). Administration of ligustroflavone (30 mg/kg, i.g.) 15 min before ischemia evidently improved neurological function, reduced infarct volume, and decreased the levels of necroptosis-associated proteins except the RIPK1. Consistently, hypoxia-cultured PC12 cells (O

Indexed as

AnimalsApigeninBrainCell SurvivalGlycosidesInfarction, Middle Cerebral ArteryMaleNecroptosisNeuroprotective AgentsPC12 CellsProtein KinasesRatsRats, Sprague-DawleyReceptor-Interacting Protein Serine-Threonine KinasesSignal TransductionStrokeApigeninGlycosidesligustroflavoneMLKL protein, ratNeuroprotective AgentsProtein KinasesReceptor-Interacting Protein Serine-Threonine KinasesLigustroflavoneMixed lineage kinase domain-like (MLKL)NecroptosisReceptor-interacting protein kinase 1 (RIPK1)Receptor-interacting protein kinase 3 (RIPK3)

Identifiers

PMID31055628
OpenAlexW2942884587

What OpenQuestion holds

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Registered trials

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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.