Evidence map›Paper›PMID 33034242›Full record

ArticleBioengineered2020

Loganin inhibits macrophage M1 polarization and modulates sirt1/NF-κB signaling pathway to attenuate ulcerative colitis.

Shi Liu, Hui Shen, Jiyan Li, Ying Gong, Haidong Bao, Jingyuan Zhang, Lanqing Hu, Zhengpeng Wang, Jian Gong

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.3field-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

46 citing papers in PubMed, 76 citations in OpenAlex.

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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 2 institutions in 1 country.

Shi LiuDepartment of Gastroenterology, The First Affiliated Hospital of Dalian Medical University , Dalian, People's Republic of China.
Hui ShenDepartment of Chinese Medicine, The First Affiliated Hospital of Dalian Medical University , Dalian, People's Republic of China.
Jiyan LiDepartment of Chinese Medicine, Dalian Hospital of Traditional Chinese Medicine , Dalian, People's Republic of China.
Ying GongDepartment of Nursing, The First Affiliated Hospital of Dalian Medical University , Dalian, People's Republic of China.
Haidong BaoDepartment of Gastroenterology, The First Affiliated Hospital of Dalian Medical University , Dalian, People's Republic of China.
Jingyuan ZhangInstitute (College) of Integrative Medicine, Dalian Medical University , Dalian, People's Republic of China.
Lanqing HuInstitute (College) of Integrative Medicine, Dalian Medical University , Dalian, People's Republic of China.
Zhengpeng WangInstitute (College) of Integrative Medicine, Dalian Medical University , Dalian, People's Republic of China.
Jian GongDepartment of Gastroenterology, The First Affiliated Hospital of Dalian Medical University , Dalian, People's Republic of China.
Dalian Medical University · CNDali Traditional Chinese Medicine Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Loganin, a major bioactive iridoid glycoside derived from Cornus officinalis, exerts different beneficial biological properties. Recently, loganin has been reported to exhibit potential anti-inflammatory effects in the intestinal tissues, while the detailed mechanisms remain elusive. This study aimed to investigate whether loganin could inhibit the inflammatory response in dextran sulfate sodium (DSS)-induced ulcerative colitis (UC) and to explore possible molecular mechanisms involved in this process. Results showed that oral administration of loganin significantly decreased body weight loss, disease activity index, colon shortening, myeloperoxidase (MPO) activity and pathologic abnormalities in UC mice. Loganin obviously inhibited the mRNA and protein levels of IL-6, TNF-α and IL-1β in colon tissues from UC mice. Furthermore, loganin remarkably reduced macrophage M1 polarization in UC mice evidenced by reduced the number of F4/80 and iNOS dual-stained M1 macrophages, and the expression of M1 macrophage-related pro-inflammatory chemokines/cytokines including MCP-1, CXCL10 as well as COX-2. Further investigation showed that loganin upregulated the mRNA and protein levels of Sirt1, with the inhibition of NF-κB-p65 acetylation in colon tissues from UC mice. Moreover, Sirt1-specific inhibitor Ex527 administration abolished the anti-inflammatory and anti-macrophage M1 polarization effects of loganin in UC. Thus, loganin could inhibit M1 macrophage-mediated inflammation and modulate Sirt1/NF-κB signaling pathway to attenuate DSS-induced UC. Loganin was considered as a viable natural strategy in the treatment of UC.[Figure: see text].

Indexed as

AnimalsBlotting, WesternColitis, UlcerativeCytokinesIridoidsMacrophagesMaleMiceMice, Inbred BALB CNF-kappa BReal-Time Polymerase Chain ReactionSignal TransductionSirtuin 1CytokinesIridoidsloganinNF-kappa BSirtuin 1Loganinmacrophage M1 polarizationsirt1/NF-κB signaling pathwayulcerative colitis

Identifiers

PMID33034242
PMCPMC8291865
OpenAlexW3034835426

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.