Evidence map›Paper›PMID 39622658›Full record

ArticleParasites, hosts and diseases2024

Allyl isothiocyanate exacerbates acute toxoplasmosis through inhibition of inflammatory cytokines.

Qiu-Mei Lin, Hong-Bin Long, Jun-Ting He, Zhi-Hao Zhang, Ho-Woo Nam, Fu-Shi Quan, Qi Zhong, Xu-Qing Liu, Zhao-Shou Yang

Abstract read
In one paragraph

Article in Parasites, hosts and diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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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.

Qiu-Mei LinThe First Affiliated Hospital/The First Clinical Medicine School of Guangdong Pharmaceutical University, Guangdong Pharmaceutical University, Guangzhou 510080, China.
Hong-Bin LongThe First Affiliated Hospital/The First Clinical Medicine School of Guangdong Pharmaceutical University, Guangdong Pharmaceutical University, Guangzhou 510080, China.
Jun-Ting HeThe First Affiliated Hospital of Sun Yat-Sen University, Zhongshan Er Road, Yuexiu District, Guangzhou 510080, China.
Zhi-Hao ZhangThe First Affiliated Hospital/The First Clinical Medicine School of Guangdong Pharmaceutical University, Guangdong Pharmaceutical University, Guangzhou 510080, China.
Ho-Woo NamDepartment of Parasitology, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.
Fu-Shi QuanDepartment of Medical Zoology, School of Medicine, Kyung Hee University, Seoul 02447, Korea.
Qi ZhongThe First Affiliated Hospital/The First Clinical Medicine School of Guangdong Pharmaceutical University, Guangdong Pharmaceutical University, Guangzhou 510080, China.
Xu-Qing LiuThe First Affiliated Hospital/The First Clinical Medicine School of Guangdong Pharmaceutical University, Guangdong Pharmaceutical University, Guangzhou 510080, China.
Zhao-Shou YangThe First Affiliated Hospital/The First Clinical Medicine School of Guangdong Pharmaceutical University, Guangdong Pharmaceutical University, Guangzhou 510080, China.

Funding

Science and Technology Program of Guangzhou 202103000051
6 · The paper itself

Abstract

Allyl isothiocyanate (AITC) is a natural product commonly used in food preservation and pharmaceutical applications. Toxoplasmosis, caused by the protozoan pathogen Toxoplasma gondii, is prevalent globally while the impact of AITC on toxoplasmosis is unclear. We explored the effect of AITC on acute toxoplasmosis. We infected C57BL/6 mice with T. gondii type I RH strain following AITC administration. On the 4th day after infection, which corresponds to the initial stage of infection, we collected serum for the determination of inflammatory cytokine levels. The mice serum of the AITC-administered group contained significantly lower levels of granulocyte colony-stimulating factor, interferon-gamma, interleukin (IL)-23 subunit p19, IL-4, IL-6, and monocyte chemoattractant protein-1. The lifespan of the mice in the AITC-administered group was significantly reduced. In vitro experiments showed that AITC promoted the proliferation of intracellular T. gondii accompanied by the inhibition of IL-4, IL-1β, and IL-6 production in RAW264.7 macrophages. Our results showed that AITC facilitated T. gondii infection in the early stage by inhibiting the production of several inflammatory cytokines.

Indexed as

CytokinesIsothiocyanatesMice, Inbred C57BLToxoplasmaAnimalsDisease Models, AnimalFemaleMacrophagesMiceRAW 264.7 CellsToxoplasmosisToxoplasmosis, Animalallyl isothiocyanateCytokinesIsothiocyanatesacute toxoplasmosisallyl isothiocyanateinflammatory cytokinepathogenToxoplasma gondii

Identifiers

PMID39622658
PMCPMC11614490

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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.