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RESEARCH PAPER / 2025-01-03

Protective effects of methylnissolin and methylnissolin-3-O-β-d-glucopyranoside on TNF-α-induced inflammation in human dermal fibroblasts.

Yea Jung Choi, Xiaohua Wu, Sullim Lee, Jae Sung Pyo, Jaejin Cho, Shugeng Cao, Ki Sung Kang

Department of Preventive Medicine, College of Korean Medicine, Gachon University, Seongnam 13120, Republic of Korea. · pubmed

Abstract

Methylnissolin-3-O-β-d-glucopyranoside (MNG) and methylnissolin (MN) are pterocarpan derivatives that are found in plants, such as Astragalus membranaceus. There are limited existing studies on the potential health benefits of MNG, and currently there is no evidence to suggest that MNG has any impact on skin-aging. Tumor necrosis factor-alpha (TNF-α) plays a significant role in skin aging by promoting chronic inflammation, damaging skin cells, and impairing the skin's natural repair mechanisms. Targeting TNF-α or its downstream signaling pathways may be a promising strategy for preventing or reversing skin-aging. We tested the effect of MNG and MN on skin-aging by inducing cell inflammation and oxidative stress with TNF-α in HDFs. MNG and MN significantly reduced the TNF-α-induced secretion of matrix metalloproteinase-1 (MMP-1). However, MNG has more beneficial compound for oral administration than MN in pharmacokinetics analysis. The mechanism underlying the anti-skin-aging effect of MNG is related to the suppression of TNF-α-induced reactive oxygen species (ROS) generation and mitogen-activated protein kinase (MAPKs) phosphorylation. Our results suggest that MNG is a potential candidate for preventing skin-aging induced by TNF-α.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

Methylnissolin-3-O-β-d-glucopyranoside (MNG) may prevent skin aging by reducing TNF-α-induced inflammation and oxidative stress in human dermal fibroblasts. The paper addresses a potential mechanism for mitigating skin aging, which is a key aspect of longevity research.

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