4.7 Article

18?-Glycyrrhetinic acid monoglucuronide (GAMG) alleviates single-walled carbon nanotubes (SWCNT)-induced lung inflammation and fibrosis in mice through PI3K/AKT/NF-?B signaling pathway

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ecoenv.2022.113858

关键词

Glycyrrhizin; Inflammation; Pulmonaryfibrosis; Signalingpathway; Single-walled carbon nanotubes (SWCNT); Glycyrrhizic acid 3-O-mono-?-D-glucuronide (GAMG)

资金

  1. Natural Science Foundation of Anhui Provincial Department of Education [KJ2019ZD21]
  2. Anhui Provincial Natural Science Foundation [2008085MH261, 2008085MH272]
  3. Research Fund of Anhui Medical University [2021xkj119]

向作者/读者索取更多资源

Carbon nanotubes are widely used in various applications, but inhalation can lead to health problems. Research shows that Glycyrrhetinic acid 3-O-mono-beta-D-glucuronide (GAMG) can alleviate lung inflammation and fibrosis induced by carbon nanotubes, making it a potential therapeutic option.
Carbon nanotubes (CNTs) have become far and wide used in a number of technical and merchant applications as a result of substantial advances in nanotechnology, therein single-walled carbon nanotubes (SWCNT) are one of the most promising nanoparticles. Inhaling CNTs has been linked to a variety of health problems, including lung fibrosis. Glycyrrhetinic acid 3-O-mono-beta-D-glucuronide (GAMG), a natural sweetener, has anti-inflammatory and antioxidant capacities. The purpose of this study was to evaluate the potential for GAMG to alleviate SWCNT-induced lung inflammation and fibrosis. During days 3-28 after SWCNT intratracheal administration, we observed a remarkable increase of IL-1 beta, IL-6 and TNF-alpha in bronchoalveolar lavage fluid (BALF) on day 3 and collagen deposition on day 28. GAMG treatment remarkably ameliorated SWCNT-induced pulmonary fibrosis and attenuated SWCNT-induced inflammation and collagen deposition, and suppressed the activation of PI3K/ AKT/NF-kappa B signaling pathway in the lungs. Therefore, GAMG has a therapeutic potential for the treatment of SWCNT-induced pulmonary fibrosis. Targeting PI3K/AKT/NF-kappa B signaling pathway may be a potential thera-peutic approach to treat pulmonary fibrosis in mice with SWCNT.

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