Evidence map›Paper›PMID 42113086›Full record

ArticleGenes & genomics2026

Anti-inflammatory activity and antioxidant capacity of Clerodendrum japonicum (Thunb.) sweet extract in LPS-stimulated macrophages.

Jeongeun Noh, Kyeoungtae Park, Fred Pitisopa, Myknee Qusa Sirikolo, Jung Jin Kim, Sung-Suk Suh, Jong Bae Seo

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Article in Genes & genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Jeongeun Noh *Department of Biomedicine, Health & Life Convergence Sciences, BK21 Four, Biomedical and Healthcare Research Institute, Mokpo National University, Muan-Gun, Jeonnam, 58554, Republic of Korea.
Kyeoungtae Park *Department of Biomedicine, Health & Life Convergence Sciences, BK21 Four, Biomedical and Healthcare Research Institute, Mokpo National University, Muan-Gun, Jeonnam, 58554, Republic of Korea.
Fred PitisopaMinistry of Forestry and Research, National Herbarium and Botanical Garden Division, Solomon Islands, P.O. Box G24, Lengaki, West Honiara, Solomon Islands.
Myknee Qusa SirikoloMinistry of Forestry and Research, National Herbarium and Botanical Garden Division, Solomon Islands, P.O. Box G24, Lengaki, West Honiara, Solomon Islands.
Jung Jin KimDepartment of Biosciences, Mokpo National University, Muan-Gun, Jeonnam, 58554, Republic of Korea.
Sung-Suk SuhDepartment of Biomedicine, Health & Life Convergence Sciences, BK21 Four, Biomedical and Healthcare Research Institute, Mokpo National University, Muan-Gun, Jeonnam, 58554, Republic of Korea.
Jong Bae SeoDepartment of Biomedicine, Health & Life Convergence Sciences, BK21 Four, Biomedical and Healthcare Research Institute, Mokpo National University, Muan-Gun, Jeonnam, 58554, Republic of Korea. jbseo@mnu.ac.kr.ORCID http://orcid.org/0000-0001-5058-5156

Funding

Mokpo National University Glocal University Project in 2025
6 · The paper itself

Abstract

backgroundClerodendrum japonicum (Thunb.) Sweet is a medicinal plant native to East Asia, including Korea, Japan, and China. Its leaves have traditionally been used to relieve respiratory symptoms and inflammatory conditions. However, no studies have systematically explored its anti-inflammatory activity and antioxidant capacity.

objectiveThis study aimed to investigate the anti-inflammatory effects of C. japonicum (Thunb.) Sweet extract (CJSE) in a lipopolysaccharide (LPS)-induced inflammatory model and determine its antioxidant capacity.

methodsAnti-inflammatory activity was investigated in LPS-stimulated RAW 264.7 macrophages by evaluating nitric oxide (NO) production, inflammatory gene expression, and related signaling pathways. Antioxidant capacity was determined using 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical scavenging assays and by determining total phenolic and flavonoid contents.

resultsCJSE reduced LPS-induced NO production in a dose-dependent manner without detectable cytotoxicity. CJSE also decreased the expression of key inflammatory mediators, including inducible nitric oxide synthase and cyclooxygenase-2, and proinflammatory cytokine genes, such as tumor necrosis factor-α, interleukin-6, and interferon-β. Mechanistically, CJSE was associated with reduced phosphorylation of extracellular signal-regulated kinase (ERK) and nuclear factor-kappa B (NF-κB) in LPS-stimulated cells. Moreover, CJSE demonstrated strong DPPH and ABTS radical scavenging activities and contained substantial levels of phenolic and flavonoid compounds, which supported its antioxidant potential.

conclusionCJSE suppresses LPS-induced inflammatory responses in macrophages and exhibits remarkable antioxidant capacity, suggesting that it could serve as a potential natural source of bioactive compounds for managing inflammation and oxidative stress.

Indexed as

Anti-Inflammatory AgentsAntioxidantsClerodendrumMacrophagesPlant ExtractsAnimalsInflammationLipopolysaccharidesMiceNitric OxideNitric Oxide Synthase Type IIRAW 264.7 CellsAnti-Inflammatory AgentsAntioxidantsLipopolysaccharidesNitric OxideNitric Oxide Synthase Type IIPlant ExtractsAntioxidantClerodendrum japonicumInflammationLPSNitric oxide

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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.