Evidence map›Paper›PMID 34204220›Full record

ArticleMarine drugs2021

Astaxanthin Protects Dendritic Cells from Lipopolysaccharide-Induced Immune Dysfunction.

Yinyan Yin, Nuo Xu, Yi Shi, Bangyue Zhou, Dongrui Sun, Bixia Ma, Zhengzhong Xu, Jin Yang, Chunmei Li

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

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  10. Blocking CD40 Alleviates Th1 and Th17 Cell Responses in Elastin Peptide-Induced Murine Emphysema.International journal of chronic obstructive pulmonary disease · 2023
    Article
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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

9 authors at 1 institution in 1 country.

Yinyan YinCollege of Medicine, Yangzhou University, Yangzhou 225009, China.
Nuo XuCollege of Medicine, Yangzhou University, Yangzhou 225009, China.
Yi ShiCollege of Medicine, Yangzhou University, Yangzhou 225009, China.
Bangyue ZhouCollege of Medicine, Yangzhou University, Yangzhou 225009, China.
Dongrui SunCollege of Medicine, Yangzhou University, Yangzhou 225009, China.
Bixia MaCollege of Food Science and Engineering, Yangzhou University, Yangzhou 225009, China.
Zhengzhong XuJiangsu Key Laboratory of Zoonosis, Yangzhou University, Yangzhou 225009, China.
Jin YangClinical Medical College, Yangzhou University, Yangzhou 225001, China.
Chunmei LiCollege of Food Science and Engineering, Yangzhou University, Yangzhou 225009, China.
Yangzhou University · CN

Funding

a project funded by the Priority Academic Program Development of Jiangsu Higher Education (PAPD) (2018) NO. 87-169the Agricultural Science & Technology Independent Innovation Fund of Jiangsu Province CX(20)3092the National Natural Science Foundation of China 31600113the National Natural Science Foundation of China 31800284the Open Project Program of Jiangsu Key Laboratory of Zoonosis R1909
6 · The paper itself

Abstract

Astaxanthin, originating from seafood, is a naturally occurring red carotenoid pigment. Previous studies have focused on its antioxidant properties; however, whether astaxanthin possesses a desired anti-inflammatory characteristic to regulate the dendritic cells (DCs) for sepsis therapy remains unknown. Here, we explored the effects of astaxanthin on the immune functions of murine DCs. Our results showed that astaxanthin reduced the expressions of LPS-induced inflammatory cytokines (TNF-α, IL-6, and IL-10) and phenotypic markers (MHCII, CD40, CD80, and CD86) by DCs. Moreover, astaxanthin promoted the endocytosis levels in LPS-treated DCs, and hindered the LPS-induced migration of DCs via downregulating CCR7 expression, and then abrogated allogeneic T cell proliferation. Furthermore, we found that astaxanthin inhibited the immune dysfunction of DCs induced by LPS via the activation of the HO-1/Nrf2 axis. Finally, astaxanthin with oral administration remarkably enhanced the survival rate of LPS-challenged mice. These data showed a new approach of astaxanthin for potential sepsis treatment through avoiding the immune dysfunction of DCs.

Indexed as

AnimalsAnti-Inflammatory AgentsBiomarkersCell MovementCytokinesDendritic CellsEndocytosisImmunosuppressive AgentsLipopolysaccharidesMaleMiceMice, Inbred C57BLSepsisXanthophyllsAnti-Inflammatory AgentsastaxanthineBiomarkersCytokinesImmunosuppressive AgentsLipopolysaccharidesXanthophyllsastaxanthindendritic cellsimmune dysfunctionlipopolysaccharidesepsis

Identifiers

PMID34204220
PMCPMC8235365
OpenAlexW3170542104

What OpenQuestion holds

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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.