<i>Alnus Sibirica</i> Extracts Suppress the Expression of Inflammatory Cytokines Induced by Lipopolysaccharides, Tumor Necrosis Factor-α, and Interferon-γ in Human Dermal Fibroblasts
Jeongyoon Choi,
Sunghee Moon,
Hyemi Bae,
Young-Won Kim,
Donghee Lee,
Seongtae Kim,
Yelim Seo,
Hye Soo Wang,
Young Wook Choi,
Min Won Lee,
Jae-Hong Ko,
Inja Lim,
Hyoweon Bang
Affiliations
Jeongyoon Choi
Department of Physiology, College of Medicine, Chung-Ang University, Seoul 06973, Korea
Sunghee Moon
Department of Physiology, College of Medicine, Chung-Ang University, Seoul 06973, Korea
Hyemi Bae
Department of Physiology, College of Medicine, Chung-Ang University, Seoul 06973, Korea
Young-Won Kim
Department of Physiology, College of Medicine, Chung-Ang University, Seoul 06973, Korea
Donghee Lee
Department of Physiology, College of Medicine, Chung-Ang University, Seoul 06973, Korea
Seongtae Kim
Department of Physiology, College of Medicine, Chung-Ang University, Seoul 06973, Korea
Yelim Seo
Department of Physiology, College of Medicine, Chung-Ang University, Seoul 06973, Korea
Hye Soo Wang
Laboratory of Pharmacognosy and Natural Product based Medicine, College of Pharmacy, Chung-Ang University, Seoul 06973, Korea
Young Wook Choi
College of Pharmacy, Chung-Ang University, Seoul 06973, Korea
Min Won Lee
Laboratory of Pharmacognosy and Natural Product based Medicine, College of Pharmacy, Chung-Ang University, Seoul 06973, Korea
Jae-Hong Ko
Department of Physiology, College of Medicine, Chung-Ang University, Seoul 06973, Korea
Inja Lim
Department of Physiology, College of Medicine, Chung-Ang University, Seoul 06973, Korea
Hyoweon Bang
Department of Physiology, College of Medicine, Chung-Ang University, Seoul 06973, Korea
The effects of Alnus sibirica (AS) extracts on cytokine expression induced by inflammatory stimulants were examined in human dermal fibroblasts (HDFs) and RAW264.7 cells. The anti-oxidative effect and effect on cell viability of AS extracts were evaluated, and four extracts with the highest anti-oxidative effects were selected. HDFs and RAW264.7 cells were treated with inflammatory stimulants, and the expression of cytokines involved in acute (IL-6 and IL-10) and chronic (IL-18) inflammation, the initiation of the immune response (IL-33), and non-specific immune responses (IL-1β, IL-8, and TNF-α) were determined using a reverse-transcription polymerase chain reaction. LPS increased the expression of all the cytokines, except for IL-18; however, AS extracts, particularly AS2 and AS4, reduced this increase, and TNF-α treatment markedly increased the expression of cytokines related to non-specific immune responses. IFN-γ treatment induced no significant changes, except for increased IL-33 expression in HDFs. AS extracts inhibited the increase in the expression of IL-33 and other cytokines in HDFs. Thus, the exposure of HDFs and RAW264.7 cells to inflammatory stimulants increased the expression of cytokines related to all the inflammatory processes. HDFs are involved not only in simple tissue regeneration but also in inflammatory reactions in the skin. AS2 and AS4 may offer effective therapy for related conditions.