<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE326nnn/GSE326538/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE326538</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Aqueous Artemisia argyi extract mitigates acute lung injury by coordinating gut microbiota, metabolic homeostasis, and pulmonary inflammatory signaling</name><description>Background: Artemisia argyi is a traditional medicinal herb with established anti-inflammatory and immunomodulatory properties. Its aqueous extract (AEAA), enriched in water-soluble bioactive constituents, exhibits favorable safety and bioavailability; however, its potential protective effects against acute lung injury (ALI) and its associations with systemic immunometabolic regulation remain incompletely understood. Methods: An LPS-induced ALI mouse model was established following 28 days of AEAA pretreatment. Lung histopathology, pulmonary edema, and inflammatory cytokines were evaluated. Integrated multi-omics analyses—including gut microbiota profiling, untargeted metabolomics of colonic contents and serum, and lung transcriptomics—were performed to characterize treatment-associated microbial, metabolic, and transcriptional alterations.Results: Lung transcriptomic profiling suggested attenuation of LPS-associated transcriptional signatures related to NF-κB, MAPK, Toll-like receptor, and PI3K–AKT signaling pathways. Cross-omics integration further revealed coordinated associations among microbial shifts, metabolic remodeling, and pulmonary inflammatory gene expression.Conclusion: These findings suggest that aqueous Artemisia argyi extract is associated with mitigation of LPS-induced acute lung injury, accompanied by coordinated alterations in gut microbiota composition, host metabolic profiles, and pulmonary inflammatory gene expression. Although causal relationships were not established, this integrated multi-omics analysis provides a systems-level, hypothesis-generating framework supporting the potential of AEAA as a multi-target botanical candidate for ALI.</description><dates><publication>2026/04/05</publication></dates><accession>GSE326538</accession><cross_references><GSM>GSM9634106</GSM><GSM>GSM9634107</GSM><GSM>GSM9634108</GSM><GSM>GSM9634109</GSM><GSM>GSM9634098</GSM><GSM>GSM9634110</GSM><GSM>GSM9634099</GSM><GSM>GSM9634088</GSM><GSM>GSM9634111</GSM><GSM>GSM9634100</GSM><GSM>GSM9634089</GSM><GSM>GSM9634101</GSM><GSM>GSM9634102</GSM><GSM>GSM9634103</GSM><GSM>GSM9634104</GSM><GSM>GSM9634105</GSM><GSM>GSM9634090</GSM><GSM>GSM9634091</GSM><GSM>GSM9634092</GSM><GSM>GSM9634093</GSM><GSM>GSM9634094</GSM><GSM>GSM9634095</GSM><GSM>GSM9634096</GSM><GSM>GSM9634097</GSM><GPL>24247</GPL><GSE>326538</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>