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Background/objectives: Atopic dermatitis (AD) is a prevalent chronic skin condition, especially in young children, with rising incidence in developed countries. AD causes repeated scratching, and thus affecting quality of life. This study evaluated the effects and mechanisms of the probiotic GKK1 on AD symptoms in mice.
Methods: Five-week-old BALB/c mice were divided into four groups ( = 8): control, AD, low-dose GKK1 (10 CFU/day), and high-dose GKK1 (10 CFU/day). GKK1 was intragastrically administered daily for 42 days. AD symptoms, skin histology, serum antibodies, inflammatory cytokine levels, gut microbiota composition, and short-chain fatty acids (SCFAs) in the intestines were assessed.
Results: GKK1 showed improved skin appearance and reduced inflammation in AD mice, with high-dose GKK1 significantly reducing histological inflammation. The GKK1 treatment upregulated splenic interleukin (IL)-2, suppressed IL-4, IL-5 and IL-17 levels and increased intestinal and spp., contributing to higher SCFAs production in intestine.
Conclusion: Oral GKK1 effectively ameliorated AD symptoms and reduced inflammation in mice. Therefore, GKK1 may serve as a potential treatment for AD.
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http://dx.doi.org/10.3389/fmicb.2025.1566594 | DOI Listing |
Front Microbiol
June 2025
Department of Animal Science, National Chung Hsing University, Taichung, Taiwan.
Background/objectives: Atopic dermatitis (AD) is a prevalent chronic skin condition, especially in young children, with rising incidence in developed countries. AD causes repeated scratching, and thus affecting quality of life. This study evaluated the effects and mechanisms of the probiotic GKK1 on AD symptoms in mice.
View Article and Find Full Text PDFJ Microbiol Biotechnol
October 2024
Biotech Research Institute, Grape King Bio Ltd, Taoyuan City 325, Taiwan.
In response to the growing demand for immune-related products, this study evaluated the safety and immune-modulating potential of three newly discovered strains (GKM3, GKK1, and GKD7) through toxicity tests and whole-genome sequencing. Safety evaluations, including the analysis of antimicrobial resistance genes, virulence factors, plasmids, and prophages, classified these strains as safe for human consumption. Acute oral toxicity tests further supported their safety.
View Article and Find Full Text PDFJ Antimicrob Chemother
May 2014
Department of Molecular Cell Biology, Samsung Biomedical Research Institute, Sungkyunkwan University School of Medicine, Suwon, South Korea.
Objectives: The emergence of colistin-resistant Pseudomonas aeruginosa is becoming a serious concern worldwide. We investigated genetic variations involved in the acquisition and loss of colistin resistance in three clinical isogenic P. aeruginosa isolates (GKK-1, GKK-2 and GKK-3) recovered from a single patient and assessed their impacts on colistin resistance.
View Article and Find Full Text PDF