Evidence map›Paper›PMID 25623758›Full record

ArticleJournal of translational medicine2015

Protective effects of astaxanthin against ischemia/reperfusion induced renal injury in mice.

Xuefeng Qiu, Kai Fu, Xiaozhi Zhao, Yanting Zhang, Yimin Yuan, Shiwei Zhang, Xiaoping Gu, Hongqian Guo

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 69 citations in OpenAlex.

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  15. Potential of natural astaxanthin in alleviating the risk of cytokine storm in COVID-19.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2020
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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

8 authors at 2 institutions in 1 country.

Xuefeng QiuDepartment of Urology, Affiliated Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing, 210008, China. Xuefeng_qiu@163.com.
Kai FuDepartment of Urology, Affiliated Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing, 210008, China. Kaifu1988@yeah.net.
Xiaozhi ZhaoDepartment of Urology, Affiliated Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing, 210008, China. dr.zxz@hotmail.com.
Yanting ZhangState Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing, 210093, China. zgam90@163.com.
Yimin YuanDepartment of Urology, Affiliated Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing, 210008, China. yuanym6666@163.com.
Shiwei ZhangDepartment of Urology, Affiliated Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing, 210008, China. zsw999@hotmail.com.
Xiaoping GuDepartment of Anesthesiology, Affiliated Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing, 210008, China. xiaopinggu1@gmail.com.
Hongqian GuoDepartment of Urology, Affiliated Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing, 210008, China. dr.guohongqian@gmail.com.
Nanjing Drum Tower Hospital · CNNanjing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Astaxanthin (ATX) is a powerful antioxidant that occurs naturally in a wide variety of living organisms. Previous studies have shown that ATX has effects of eliminating oxygen free radicals and can protect organs from ischemia/reperfusion (IR) induced injury. The present study was designed to further investigate the protective effects of ATX on oxidative stress induced toxicity in tubular epithelial cells and on IR induced renal injury in mice. ATX, at a concentration of 250 nM, attenuated 100 μM H2O2-inudced viability decrease of tubular epithelial cells. In vivo, ATX preserved renal function 12 h or 24 h post IR. Pretreatment of ATX via oral gavage for 14 consecutive days prior to IR dramatically prevented IR induced histological damage 24 h post IR. Histological results showed that the pathohistological score, number of apoptotic cells, and the expression of α-smooth muscle actin were significantly decreased by pretreatment of ATX. In addition, oxidative stress and inflammation in kidney samples were significantly reduced by ATX 24 h post IR. Taken together, the current study suggests that pretreatment of ATX is effective in preserving renal function and histology via antioxidant activity.

Indexed as

ActinsAnimalsAntioxidantsApoptosisCells, CulturedCell SurvivalEnzyme-Linked Immunosorbent AssayFree RadicalsHumansHydrogen PeroxideInflammationKidneyKidney TubulesMaleMalondialdehydeMiceActinsAntioxidantsastaxanthineFree RadicalsHydrogen PeroxideMalondialdehydeSuperoxide DismutaseXanthophylls

Identifiers

PMID25623758
PMCPMC4323259
OpenAlexW2125567771

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.