TY - JOUR
T1 - Impact of smoking on gut microbiota and short-chain fatty acids in human and mice
T2 - Implications for COPD
AU - Otake, Shiro
AU - Chubachi, Shotaro
AU - Miyamoto, Junki
AU - Haneishi, Yuri
AU - Arai, Tetsuya
AU - Iizuka, Hideto
AU - Shimada, Takashi
AU - Sakurai, Kaori
AU - Okuzumi, Shinichi
AU - Kabata, Hiroki
AU - Asakura, Takanori
AU - Miyata, Jun
AU - Irie, Junichiro
AU - Asano, Koichiro
AU - Nakamura, Hidetoshi
AU - Kimura, Ikuo
AU - Fukunaga, Koichi
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2025/4
Y1 - 2025/4
N2 - We aimed to elucidate the dynamic changes in short-chain fatty acids (SCFA) produced by the gut microbiota following smoking exposure and their role in chronic obstructive pulmonary disease (COPD) pathogenesis. SCFA concentrations were measured in human plasma, comparing non-smokers (n = 6) and smokers (n = 12). Using a mouse COPD model induced by cigarette smoke exposure or elastase-induced emphysema, we modulated SCFA levels through dietary interventions and antibiotics to evaluate their effects on inflammation and alveolar destruction. Human smokers showed lower plasma SCFA concentrations than non-smokers, with plasma propionic acid positively correlating with forced expiratory volume in 1 s/forced vital capacity. Three-month smoking-exposed mice demonstrated altered gut microbiota and significantly reduced fecal SCFA concentrations compared to air-exposed controls. In these mice, a high-fiber diet increased fecal SCFAs and mitigated inflammation and alveolar destruction, while antibiotics decreased fecal SCFAs and exacerbated disease features. However, in the elastase-induced model, fecal SCFA concentration remained unchanged, and high-fiber diet or antibiotic interventions had no significant effect. These findings suggest that smoking exposure alters gut microbiota and SCFA production through its systemic effects. The anti-inflammatory properties of SCFAs may play a role in COPD pathogenesis, highlighting their potential as therapeutic targets.
AB - We aimed to elucidate the dynamic changes in short-chain fatty acids (SCFA) produced by the gut microbiota following smoking exposure and their role in chronic obstructive pulmonary disease (COPD) pathogenesis. SCFA concentrations were measured in human plasma, comparing non-smokers (n = 6) and smokers (n = 12). Using a mouse COPD model induced by cigarette smoke exposure or elastase-induced emphysema, we modulated SCFA levels through dietary interventions and antibiotics to evaluate their effects on inflammation and alveolar destruction. Human smokers showed lower plasma SCFA concentrations than non-smokers, with plasma propionic acid positively correlating with forced expiratory volume in 1 s/forced vital capacity. Three-month smoking-exposed mice demonstrated altered gut microbiota and significantly reduced fecal SCFA concentrations compared to air-exposed controls. In these mice, a high-fiber diet increased fecal SCFAs and mitigated inflammation and alveolar destruction, while antibiotics decreased fecal SCFAs and exacerbated disease features. However, in the elastase-induced model, fecal SCFA concentration remained unchanged, and high-fiber diet or antibiotic interventions had no significant effect. These findings suggest that smoking exposure alters gut microbiota and SCFA production through its systemic effects. The anti-inflammatory properties of SCFAs may play a role in COPD pathogenesis, highlighting their potential as therapeutic targets.
KW - Chronic obstructive pulmonary disease
KW - Gut-lung axis
KW - Microbiota
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U2 - 10.1016/j.mucimm.2024.12.006
DO - 10.1016/j.mucimm.2024.12.006
M3 - Article
AN - SCOPUS:85212625004
SN - 1933-0219
VL - 18
SP - 353
EP - 365
JO - Mucosal Immunology
JF - Mucosal Immunology
IS - 2
ER -