Evidence map›Paper›PMID 27830717›Full record

ArticleScientific reports2016

Effect of Heme Oxygenase-1 on Mitofusin-1 protein in LPS-induced ALI/ARDS in rats.

Jianbo Yu, Ying Wang, Zhen Li, Shuan Dong, Dan Wang, Lirong Gong, Jia Shi, Yuan Zhang, Daquan Liu, Rui Mu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 51 citations in OpenAlex.

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  16. Hydromorphone Protects against COOxidative medicine and cellular longevity · 2021
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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

10 authors at 3 institutions in 1 country.

Jianbo YuDepartment of Anesthesiology, Tianjin Nan Kai Hospital, Tianjin Medical University, Tianjin, 300100, China.
Ying WangDepartment of Anesthesiology, Tianjin Nan Kai Hospital, Tianjin Medical University, Tianjin, 300100, China.
Zhen LiDepartment of Anesthesiology, Tianjin Nan Kai Hospital, Tianjin Medical University, Tianjin, 300100, China.
Shuan DongDepartment of Anesthesiology, Tianjin Nan Kai Hospital, Tianjin Medical University, Tianjin, 300100, China.
Dan WangDepartment of Anesthesiology, Tianjin Nan Kai Hospital, Tianjin Medical University, Tianjin, 300100, China.
Lirong GongDepartment of Anesthesiology, Tianjin Nan Kai Hospital, Tianjin Medical University, Tianjin, 300100, China.
Jia ShiDepartment of Anesthesiology, Tianjin Nan Kai Hospital, Tianjin Medical University, Tianjin, 300100, China.
Yuan ZhangDepartment of Anesthesiology, Tianjin Nan Kai Hospital, Tianjin Medical University, Tianjin, 300100, China.
Daquan LiuInstitute of Acute Abdominal Diseases of Integrated Traditional Chinese and Western Medicine, Tianjin, 300100, China.
Rui MuDepartment of Anesthesiology, Tianjin Nan Kai Hospital, Tianjin Medical University, Tianjin, 300100, China.
Tianjin Nankai Hospital · CNTianjin Medical University · CNDeleted Institution

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a common and important oxidative stress in the lung. Mitochondrial fusion responds to the normal morphology and function of cells and is finely regulated by mitochondrial fusion proteins, such as mitofusin-1 protein (Mfn1), mitofusin-2 protein (Mfn2) and optical atrophy 1 (OPA1). Additionally, Mfn1 has been identified as the most important protein in mitochondrial fusion. Heme oxygenase-1 (HO-1) is a stress-inducible protein that plays a critical role in protecting against oxidative stress. However, whether the protection of HO-1 is related to mitochondrial fusion is still a question. Thus, our in vitro and in vivo experiments aimed to identify the relationship between HO-1 and Mfn1. Here, we used Hemin and ZnPP-IX as treatments in an in vivo experiment. Then, HO-1 and Mfn1 were measured using RT-PCR and Western blotting. Supernatants were analyzed for MDA, SOD, and ROS. Our results implied that HO-1 upregulation suppressed oxidative stress induced by LPS, and the possible mechanism could be associated with Mfn1 and the PI3K/Akt pathway.

Indexed as

Signal TransductionAcute Lung InjuryAnimalsGene Expression Regulation, EnzymologicHeme Oxygenase (Decyclizing)HeminLipopolysaccharidesMaleMembrane ProteinsMitochondrial ProteinsOxidative StressProtoporphyrinsRatsRats, Sprague-DawleyRespiratory Distress SyndromeUp-RegulationHeme Oxygenase (Decyclizing)HeminHmox1 protein, ratLipopolysaccharidesMembrane ProteinsMfn1 protein, ratMitochondrial ProteinsProtoporphyrinszinc protoporphyrin

Identifiers

PMID27830717
PMCPMC5103207
OpenAlexW2552995152

What OpenQuestion holds

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LicenceCC BY
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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.