Evidence map›Paper›PMID 41149579›Full record

ArticleMarine drugs2025

Therapeutic Potential of DPHC, A Brown Seaweed Polyphenol, Against TNF-α-Induced Inflammatory Muscle Loss.

Minji Kim, Won-Woo Lee, Kil-Nam Kim, Young-Mog Kim, You-Jin Jeon, Fengqi Yang, Seo-Young Kim, Hyo-Geun Lee

Abstract read
In one paragraph

Article in Marine drugs, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Article
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.

Minji KimResearch Center for Marine Integrated Bionics Technology, Pukyong National University, Busan 48513, Republic of Korea.ORCID 0000-0002-8926-9449
Won-Woo LeeDivision of Practical Research, Honam National Institute of Biological Resources, 99, Gohadoan-gil, Mokpo-si 58762, Republic of Korea.
Kil-Nam KimGwangju Center, Korea Basic Science Institute, Gwangju 61751, Republic of Korea.ORCID 0000-0002-7712-7697
Young-Mog KimResearch Center for Marine Integrated Bionics Technology, Pukyong National University, Busan 48513, Republic of Korea.ORCID 0000-0002-2465-8013
You-Jin JeonDepartment of Marine Life Science, Jeju National University, Jeju 63243, Republic of Korea.ORCID 0000-0003-3299-7266
Fengqi YangDepartment of Marine Life Science, Jeju National University, Jeju 63243, Republic of Korea.
Seo-Young KimDivision of Practical Research, Honam National Institute of Biological Resources, 99, Gohadoan-gil, Mokpo-si 58762, Republic of Korea.
Hyo-Geun LeeNational Marine Biodiversity Institute of Korea, 75, Jangsan-ro 101-gil, Janghang-eup, Seocheon 33362, Republic of Korea.

Funding

Ministry of Oceans and Fisheries KIMST-20220128National Marine Biodiversity Institute of Korea 2025M00500
6 · The paper itself

Abstract

Inflammatory muscle loss results from excessive inflammatory responses, causing muscle damage and weakness. In the current investigation, we evaluated the protective effects of diphlorethohydroxycarmalol (DPHC) against tumor necrosis factor-alpha (TNF-α)-induced skeletal muscle inflammation and muscle loss and elucidated the underlying mechanisms. Furthermore, the effect of DPHC on swimming performance was confirmed under TNF-α-induced inflammatory muscle loss-conditioned zebrafish by assessing the swimming number, distance moved, time spent swimming, frequency of swimming zebrafishes in an upstream swim track (Zone A). In vivo behavioral endurance test results indicated that TNF-α treatment significantly decreased the number of swimming zebrafish and swimming distance in Zone A compared with the Control. Meanwhile, the DPHC treatment significantly increased the number of swimming zebrafish and swimming distance in Zone A compared to TNF-α-induced zebrafish. These findings indicate that DPHC treatment effectively improved the swimming performance of TNF-α-induced zebrafish. In an additional study, TNF-α significantly induced inflammatory muscle loss by upregulating nuclear factor kappa light chain enhancer of activated B cells (NF-κB) mitogen activated protein kinase (MAPK) associated proteins and MuRF-1 in the skeletal muscle tissues of TNF-α-induced zebrafish. However, DPHC administration significantly counteracted TNF-α-induced inflammation and muscle loss by downregulating NF-Κb and MAPK-associated proteins, as well as the muscle degradation-related proteins MuRF-1 and MAFbx, in the skeletal muscle tissues of TNF-α-induced zebrafish. In summary, our research findings demonstrated that DPHC from

Indexed as

Anti-Inflammatory AgentsInflammationMuscle, SkeletalPhaeophyceaePolyphenolsSeaweedTumor Necrosis Factor-alphaAnimalsNF-kappa BSwimmingZebrafishAnti-Inflammatory AgentsNF-kappa BPolyphenolsTumor Necrosis Factor-alphaalgal polyphenolinflammatory muscle lossIshige okamuraepro-inflammatory cytokineswimming performance

Identifiers

PMID41149579
PMCPMC12565170

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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.