Evidence map›Paper›PMID 39529087›Full record

ArticleJournal of translational medicine2024

Mitochondrial transplantation following cardiopulmonary resuscitation improves neurological function in rats by inducing M2-type MG/MΦ polarization.

Jie Zhu, Zhen Wang, Mengda Xu, Xuyuan Ma, Maozheng Shen, Jingyu Yan, Xiang Zhou

Abstract read
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Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Jie Zhu *The First School of Clinical Medicine, Southern Medical University, Guangzhou, 510515, China.
Zhen Wang *The First School of Clinical Medicine, Southern Medical University, Guangzhou, 510515, China.
Mengda XuDepartment of Anesthesiology, General hospital of central theater command of PLA, Wuhan, 430070, China.
Xuyuan MaBase of Central Theater Command of People's Liberation Army, Hubei University of Medicine, Wuhan, China.
Maozheng ShenBase of Central Theater Command of People's Liberation Army, Hubei University of Medicine, Wuhan, China.
Jingyu YanDepartment of Anesthesiology, General hospital of central theater command of PLA, Wuhan, 430070, China.
Xiang ZhouThe First School of Clinical Medicine, Southern Medical University, Guangzhou, 510515, China. zhouxiang188483@126.com.ORCID 0000-0001-9635-8741

Funding

National Natural Science Foundation of China 81901932National Natural Science Foundation of China 82372210Natural Science Foundation of Hubei Province 2021CFB492
6 · The paper itself

Abstract

aimExplore the effects of mitochondrial transplantation (MT) after cardiopulmonary resuscitation (CPR) on the polarization of microglia/macrophages (MG/MΦ) and neurological function.

methodsSeventy-five Sprague-Dawley rats were randomly divided into five groups: sham, normal saline (NS), vehicle, mitochondria (Mito), and non-functional mitochondria (N-Mito) group. Rats in sham group underwent surgical procedures without cardiac arrest, while the other four groups underwent cardiac arrest and CPR, and then received NS, respiration buffer, mitochondrial suspension or non-functional mitochondria, immediately after the restoration of spontaneous circulation (ROSC). The number of mitochondria in the hippocampus, the morphology and structure of mitochondria in MG/MΦ, the phenotype of MG/MΦ, and hippocampal tissue injury, neuroinflammation, and neuronal apoptosis were detected on days 1 and 3 after ROSC. Neurodeficit score (NDS) was performed on days 1, 3, 7, 15 and 30 after ROSC.

resultsCompared with other groups, the number of mitochondria in the hippocampus was increased, and the morphology and structure of mitochondria in MG/MΦ were significantly improved in the Mito group. Our results show higher expression of M2-type markers in MG/MΦ and decreased hippocampal tissue damage in the Mito group. Levels of NSE and S100β in serum, and TNF-α, IL-6 in the hippocampus were decreased, while the levels of TGF-β and IL-10 were increased in the Mito group. Apoptosis rate of neurons in the Mito group was decreased and the NDS of the Mito group was higher than the other groups.

conclusionsExogenous MT can improve neurological function after CPR by promoting the polarization of MG/MΦ to M2-type cells, and this could be a potential method for brain protection after CPR.

Indexed as

Cardiopulmonary ResuscitationHippocampusMacrophagesMicrogliaMitochondriaRats, Sprague-DawleyAnimalsApoptosisCell PolarityCytokinesHeart ArrestMaleNervous SystemNeuronsPhenotypeRatsCytokinesCardiac arrestMacrophagesMicrogliaMitochondrial transplantationNeurological function

Identifiers

PMID39529087
PMCPMC11552134

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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.