Your browser doesn't support javascript.
loading
Garlic oil supplementation blocks inflammatory pyroptosis-related acute lung injury by suppressing the NF-κB/NLRP3 signaling pathway via H2S generation.
Dilxat, Tursunay; Shi, Qiang; Chen, Xiaofan; Liu, Xuxin.
Affiliation
  • Dilxat T; Xinjiang Agricultural Vocational Technological College, Changji 831100, Xinjiang, China.
  • Shi Q; Xinjiang Agricultural Vocational Technological College, Changji 831100, Xinjiang, China.
  • Chen X; Xinjiang Agricultural Vocational Technological College, Changji 831100, Xinjiang, China.
  • Liu X; Xinjiang Agricultural Vocational Technological College, Changji 831100, Xinjiang, China.
Aging (Albany NY) ; 16(7): 6521-6536, 2024 04 12.
Article in En | MEDLINE | ID: mdl-38613798
ABSTRACT
Acute lung injury (ALI) is a major cause of acute respiratory failure with a high morbidity and mortality rate, and effective therapeutic strategies for ALI remain limited. Inflammatory response is considered crucial for the pathogenesis of ALI. Garlic, a globally used cooking spice, reportedly exhibits excellent anti-inflammatory bioactivity. However, protective effects of garlic against ALI have never been reported. This study aimed to investigate the protective effects of garlic oil (GO) supplementation on lipopolysaccharide (LPS)-induced ALI models. Hematoxylin and eosin staining, pathology scores, lung myeloperoxidase (MPO) activity measurement, lung wet/dry (W/D) ratio detection, and bronchoalveolar lavage fluid (BALF) analysis were performed to investigate ALI histopathology. Real-time polymerase chain reaction, western blotting, and enzyme-linked immunosorbent assay were conducted to evaluate the expression levels of inflammatory factors, nuclear factor-κB (NF-κB), NLRP3, pyroptosis-related proteins, and H2S-producing enzymes. GO attenuated LPS-induced pulmonary pathological changes, lung W/D ratio, MPO activity, and inflammatory cytokines in the lungs and BALF. Additionally, GO suppressed LPS-induced NF-κB activation, NLRP3 inflammasome expression, and inflammatory-related pyroptosis. Mechanistically, GO promoted increased H2S production in lung tissues by enhancing the conversion of GO-rich polysulfide compounds or by increasing the expression of H2S-producing enzymes in vivo. Inhibition of endogenous or exogenous H2S production reversed the protective effects of GO on ALI and eliminated the inhibitory effects of GO on NF-κB, NLRP3, and pyroptotic signaling pathways. Overall, these findings indicate that GO has a critical anti-inflammatory effect and protects against LPS-induced ALI by suppressing the NF-κB/NLRP3 signaling pathway via H2S generation.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Sulfides / Signal Transduction / Lipopolysaccharides / NF-kappa B / Allyl Compounds / Acute Lung Injury / Pyroptosis / NLR Family, Pyrin Domain-Containing 3 Protein / Hydrogen Sulfide Language: En Journal: Aging (Albany NY) Year: 2024 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Main subject: Sulfides / Signal Transduction / Lipopolysaccharides / NF-kappa B / Allyl Compounds / Acute Lung Injury / Pyroptosis / NLR Family, Pyrin Domain-Containing 3 Protein / Hydrogen Sulfide Language: En Journal: Aging (Albany NY) Year: 2024 Type: Article Affiliation country: China