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GC-MS raw data were imported into Masshunter quantitative software (Agilent, USA, version number: v10.0.707.0). All ion fragments were automatically identificated and integrated by using default parameters,&lt;/p>&lt;p>besides, all intergration was checked manually. The metabolite concerntration of sample was calculated according to linear regression standard curve.&lt;/p></metabolite_identification_protocol><repository>MetaboLights</repository><study_status>Public</study_status><ptm_modification></ptm_modification><instrument_platform>Gas Chromatography MS - alternating - high-polarity</instrument_platform><chromatography_protocol>&lt;p>25 mg solid sample were accurately weighed into 2 mL grinding tube and add 500 µL water containing 0.5%phosphoric acid. The sample were froze and ground at 50 Hz for 3 min, repeated twice, followed by ultrasonic for 10 min and centrifugation at 4 oC and 13000 g for 15 min. Take 200 µL out the supernatant aqueous solution into a 1.5 mL centrifuge tube, then add 0.2 mL N-butanol solvent containing internal standard 2-ethylbutyric acid (10 μg/mL) for exaction. Finally,vortexl for 10 s, ultrasound at low temperature for 10 min, followed by centrifugation at 4 oC and 13000 g for 5 min and the supernatant were carefully transferred to sample vials for analysis.&lt;/p></chromatography_protocol><publication>Effect of probiotics intervention on short chain fatty acids in irradiated mice.</publication><submitter_affiliation>Fourth Military Medical University: Air Force Medical University</submitter_affiliation><submitter_name>Guiqiang Zhou</submitter_name><organism_part>serum</organism_part><organism_part>brain</organism_part><organism_part>feces</organism_part><technology_type>mass spectrometry assay</technology_type><disease></disease><extraction_protocol>&lt;p>Collect mouse feces, collect blood from the apex of the heart, and collect serum at 4 ℃ and 12000rpm/min. Extract mouse brain tissue.&lt;/p></extraction_protocol><organism>Mus musculus</organism><full_dataset_link>https://www.ebi.ac.uk/metabolights/MTBLS15754</full_dataset_link><author>Guiqiang Zhou. Fourth Military Medical University: Air Force Medical University. zgqiang0308@163.com.</author><data_transformation_protocol>&lt;p>The analysis was performed using an Agilent 8890B gas chromatography coupled to an Agilent 5977B/7000D mass selective detector with an inert electron impact (EI) ionization source and ionization voltage was 70eV (Agilent, USA) at Majorbio Bio-Pharm Technology Co. Ltd. (Shanghai, China). Analyte compounds were separated with a HP-FFAP (30 m×0.25mm×0.25 µm) capillary column, using 99.999% helium as a carrier gas at a constant flow rate (1 mL/ min). The GC column temperature was programmed to hold at 80 oC and rise to 120 oC at a rate of 40 oC per minute, then rise to 180 oC at a rate of 10 oC per minute, finally rise to 200 oC at a rate of 20 oC per minute hold at temperature of 220 oC for 3 min. The injection volume of samples was 1 µL and introduced in splitting mode (10:1) with the inlet temperature of 230 oC. The ion sources temperature was 250 oC and the quadrupole temperature temperature was 150 oC and the transfer line temperature was 240 oC . The scanning mode is Selected Ion Monitoring SIM.&lt;/p></data_transformation_protocol><study_factor>Probiotic</study_factor><study_factor>Radiation</study_factor><submitter_email>zgqiang0308@163.com</submitter_email><sample_collection_protocol>&lt;p>8 weeks after exposure to ionizing radiation and 1 week of probiotic intervention&lt;/p></sample_collection_protocol><omics_type>Metabolomics</omics_type><study_design>short-chain fatty acid</study_design><study_design>Metabolomics</study_design><study_design>ProteoWizard msconvert</study_design><study_design>Mus musculus</study_design><study_design>targeted analysis</study_design><study_design>8890B</study_design><study_design>Brain-Gut Axis</study_design><study_design>targeted metabolite profiling</study_design><study_design>brain</study_design><study_design>experimental sample</study_design><study_design>radiation</study_design><study_design>Agilent 5977B MSD</study_design><study_design>Anxiety</study_design><study_design>serum</study_design><study_design>feces</study_design><curator_keywords>short-chain fatty acid</curator_keywords><curator_keywords>Metabolomics</curator_keywords><curator_keywords>ProteoWizard msconvert</curator_keywords><curator_keywords>Mus musculus</curator_keywords><curator_keywords>targeted analysis</curator_keywords><curator_keywords>8890B</curator_keywords><curator_keywords>Brain-Gut Axis</curator_keywords><curator_keywords>targeted metabolite profiling</curator_keywords><curator_keywords>brain</curator_keywords><curator_keywords>experimental sample</curator_keywords><curator_keywords>radiation</curator_keywords><curator_keywords>Agilent 5977B MSD</curator_keywords><curator_keywords>Anxiety</curator_keywords><curator_keywords>serum</curator_keywords><curator_keywords>feces</curator_keywords><mass_spectrometry_protocol>&lt;p>The analysis was performed using an Agilent 8890B gas chromatography coupled to an Agilent 5977B/7000D mass selective detector with an inert electron impact (EI) ionization source and ionization voltage was 70eV (Agilent, USA) at Majorbio Bio-Pharm Technology Co. Ltd. (Shanghai, China). Analyte compounds were separated with a HP-FFAP (30 m×0.25mm×0.25 µm) capillary column, using 99.999% helium as a carrier gas at a constant flow rate (1 mL/ min). The GC column temperature was programmed to hold at 80 oC and rise to 120 oC at a rate of 40 oC per minute, then rise to 180 oC at a rate of 10 oC per minute, finally rise to 200 oC at a rate of 20 oC per minute hold at temperature of 220 oC for 3 min. The injection volume of samples was 1 µL and introduced in splitting mode (10:1) with the inlet temperature of 230 oC. The ion sources temperature was 250 oC and the quadrupole temperature temperature was 150 oC and the transfer line temperature was 240 oC . The scanning mode is Selected Ion Monitoring SIM.&lt;/p></mass_spectrometry_protocol></additional><is_claimable>false</is_claimable><name>Effect of probiotics intervention on short chain fatty acids in irradiated mice</name><description>&lt;p>In order to study the effect of probiotic intervention on short-chain fatty acids in irradiated mice, we collected feces, blood, and brain tissues from irradiated mice. The content of short-chain fatty acids was determined by High Performance Liquid Chromatography-mass spectrum. Further investigate the effects of ionizing radiation on the levels of short-chain fatty acids in the gut brain axis of mice, as well as the therapeutic effects of probiotics on radiation exposed mice.&lt;/p></description><dates><publication>2026-09-28</publication><submission>2026-09-21</submission></dates><accession>MTBLS15754</accession><cross_references/></HashMap>