AI Article Synopsis

  • - Kawasaki disease (KD) mainly affects young children and is marked by acute vasculitis, with increased levels of reactive oxygen species (ROS) linked to its progression, especially in coronary arteries.
  • - In this study, researchers used mice with LCWE-induced vasculitis to assess the effects of hydrogen gas inhalation, finding significant improvements in left coronary artery sizes and inflammation levels.
  • - This research is notable as it's the first to show that inhaling hydrogen gas can effectively treat coronary artery dilation related to Kawasaki disease in a mouse model.

Article Abstract

Background: Kawasaki disease (KD) is a syndrome primarily affecting young children, typically under the age of five, and is characterized by the development of acute vasculitis. Through extensive research conducted on both murine and human subjects, it has been demonstrated that heightened levels of reactive oxygen species (ROS) play a pivotal role in the development of KD, especial coronary artery lesions (CALs). Hydrogen gas exhibits potent antioxidant properties that effectively regulate ROS production and the inflammatory response.

Methods: We used cell wall extract (LCWE)-induced vasculitis in mice as an animal model of KD and treated the mice with hydrogen gas inhalation.

Results: We observed significant dilatation and higher Z scores in the left coronary artery (LCA) in D21 and D28 in mice after LCWE treatment compared to the control group ( < 0.001) and a significant resolution of LCA diameters ( < 0.01) and Z scores ( < 0.01) after treatment with inhaled hydrogen gas. We further demonstrated that serum IL-6 expression was higher in mice after LCWE treatment ( < 0.01) and IL-6 significantly decreased after inhaled hydrogen gas therapy ( < 0.001).

Conclusion: According to our literature review, this is the first report where hydrogen gas inhalation has been demonstrated to be effective for the treatment of coronary artery dilatation in a KD murine model.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11277616PMC
http://dx.doi.org/10.3390/life14070796DOI Listing

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