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[논문] Polyphenol-enriched extract from Tagetes erecta L. attenuates LPS-induced inflammation and toxicity by targeting the TLR4/MD2 signaling pathway

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논문제목(Title)

[논문] Polyphenol-enriched extract from Tagetes erecta L. attenuates LPS-induced inflammation and toxicity by targeting the TLR4/MD2 signaling pathway

학술지명(Journal)

Journal of Functional Foods

ImpactFactor

3.8

ISSN_ISBN

1756-4646

학술지볼륨권호(Volume)

117

SCI구분

SCIE

초록(Abstract)

The study investigates the medicinal properties of Tagetes erecta L. (marigold) in combating inflammation and toxicity induced by lipopolysaccharides (LPS). The polyphenol-enriched extract from T. erecta L. petals (TE) exhibited significant anti-inflammatory effects by targeting the Toll-like receptor 4 (TLR4)/myeloid differentiation factor 2 (MD2) complex, as evidenced in cellular and animal models. In vitro, TE effectively inhibited LPS induced proinflammatory mediators and key genes associated with inflammation. Molecular docking analyses suggested that constituents of TE, such as patulitrin, quercetagetin, kaempferol, patuletin, and isorhamnetin, have the potential to bind to the TLR4/MD2 complex, therefore supporting its anti-inflammatory effects. Experiments on zebrafish larvae revealed that TE mitigates LPS-induced abnormalities and mortality, as well as attenuates the expression of proinflammatory genes, highlighting its therapeutic potential. Overall, the study underscores the promising medicinal value of T. erecta L., particularly TE, in addressing LPS-induced inflammation and associated disorders, thus warranting further exploration in clinical applications.

주저자명(FirstAuthor)

Sobarathne Senel Sanjaya

공동저자명(Co-Author)

Mi Hyeon Park, Hyung Won Ryu, Yung Hyun Choi, Mi-Hwa Lee, Chang-Hee Kang d, Min-Jeong Jung, Kyoung Tae Lee, Gi-Young Kim

학술지출판일자(PublicationDate)

2024.05.06.

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공개 일자

2024-08-08

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2024-08-08
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관리자 ( 2024-08-08 ) [논문] Polyphenol-enriched extract from Tagetes erecta L. attenuates LPS-induced inflammation and toxicity by targeting the TLR4/MD2 signaling pathway

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