Natto consumption suppresses atherosclerotic plaque progression in LDL receptor-deficient mice transplanted with iRFP-expressing hematopoietic cells

Natto, known for its high vitamin K content, has been demonstrated to suppress atherosclerosis in large-scale clinical trials through a yet-unknown mechanism. In this study, we used a previously reported mouse model, transplanting the bone marrow of mice expressing infra-red fluorescent protein (iRF...

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Veröffentlicht in:Scientific reports 2023-12, Vol.13 (1), p.22469-22469, Article 22469
Hauptverfasser: Kawamata, Takeshi, Wakimoto, Arata, Nishikawa, Takanobu, Ikezawa, Masaya, Hamada, Michito, Inoue, Yuri, Kulathunga, Kaushalya, Salim, Filiani Natalia, Kanai, Maho, Nishino, Teppei, Gentleman, Kyle, Liu, Chang, Mathis, Bryan J., Obana, Nozomu, Fukuda, Shinji, Takahashi, Satoru, Taya, Yuki, Sakai, Satoshi, Hiramatsu, Yuji
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Sprache:eng
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Zusammenfassung:Natto, known for its high vitamin K content, has been demonstrated to suppress atherosclerosis in large-scale clinical trials through a yet-unknown mechanism. In this study, we used a previously reported mouse model, transplanting the bone marrow of mice expressing infra-red fluorescent protein (iRFP) into LDLR-deficient mice, allowing unique and non-invasive observation of foam cells expressing iRFP in atherosclerotic lesions. Using 3 natto strains, we meticulously examined the effects of varying vitamin K levels on atherosclerosis in these mice. Notably, high vitamin K natto significantly reduced aortic staining and iRFP fluorescence, indicative of decreased atherosclerosis. Furthermore, mice administered natto showed changes in gut microbiota, including an increase in natto bacteria within the cecum, and a significant reduction in serum CCL2 expression. In experiments with LPS-stimulated macrophages, adding natto decreased CCL2 expression and increased anti-inflammatory cytokine IL-10 expression. This suggests that natto inhibits atherosclerosis through suppression of intestinal inflammation and reduced CCL2 expression in macrophages.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-023-48562-y