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were identified by matching accurate mass, retention time and MS/MS fragmentation spectra against in-house and public databases including HMDB, KEGG, and METLIN. Identification confidence levels follow the Metabolomics Standards Initiative (MSI) reporting guidelines. Differential metabolites were defined based on variable importance in projection (VIP) greater than 1, fold change greater than 1.2 or less than 0.833, and p-value less than 0.05.&lt;/p></metabolite_identification_protocol><repository>MetaboLights</repository><study_status>Public</study_status><ptm_modification></ptm_modification><instrument_platform>Liquid Chromatography MS - positive - hilic</instrument_platform><instrument_platform>Liquid Chromatography MS - negative - hilic</instrument_platform><chromatography_protocol>&lt;p>Chromatographic separation was performed on a Vanquish UHPLC system (Thermo Fisher Scientific) using a Waters ACQUITY UPLC BEH Amide column (2.1 x 50 mm, 1.7 um) for HILIC separation. Mobile phase A was 25 mmol/L ammonium acetate and 25 mmol/L ammonium hydroxide in water (pH 9.75). Mobile phase B was acetonitrile. The gradient elution was performed at a flow rate of 0.5 mL/min. Column temperature was maintained at 45 degrees C. Injection volume was 2 uL.&lt;/p></chromatography_protocol><publication>Serum Metabolomics Reveals Stage-Dependent Metabolic Transitions During CIDR-PGF2alpha-Induced Estrus in Kazak Ewes. 10.3389/fvets.2026.1904685.</publication><submitter_name>Yaseen Ullah</submitter_name><submitter_affiliation>Shihezi University</submitter_affiliation><organism_part>serum</organism_part><technology_type>mass spectrometry assay</technology_type><disease></disease><extraction_protocol>&lt;p>Serum samples were thawed at 4 degrees C and 100 uL of each sample was mixed with 400 uL of methanol/acetonitrile (1:1, v/v) containing internal standards. Samples were vortexed for 30 s, incubated at -20 degrees C for 30 min, then centrifuged at 14000 rpm for 20 min at 4 degrees C. The supernatant was transferred and dried under nitrogen. Residues were reconstituted in 100 uL acetonitrile/water (1:1, v/v). Pooled quality control (QC) samples were prepared by mixing equal volumes of all individual samples.date this protocol description&lt;/p></extraction_protocol><organism>Ovis aries</organism><full_dataset_link>https://www.ebi.ac.uk/metabolights/MTBLS15117</full_dataset_link><author>Zhao Zongsheng. Shihezi University. zhaozongsh@shzu.edu.</author><author>Yaseen Ullah. Shihezi University. hbksons@outlook.com.</author><data_transformation_protocol>&lt;p>Raw data files were converted from instrument format to mzXML format using ProteoWizard MSConvert (v3.0.24054). Peak detection, alignment and quantification were performed by the metabolomics analysis company (Wuhan Berna Technology Co., Ltd). TIC normalization was applied to all samples prior to statistical analysis.&lt;/p></data_transformation_protocol><study_factor>Reproductive stage</study_factor><submitter_email>hbksons@outlook.com</submitter_email><sample_collection_protocol>&lt;p>Blood samples were collected from 18 Kazak ewes (6 per group) at defined reproductive stages following CIDR-PGF2alpha synchronization treatment. Serum was separated by centrifugation at 3000 rpm for 10 min at 4 degrees C and stored at -80 degrees C until analysis.e this protocol description&lt;/p></sample_collection_protocol><omics_type>Metabolomics</omics_type><study_design>Vanquish UHPLC</study_design><study_design>hydrophilic interaction chromatography</study_design><study_design>ProteoWizard msconvert</study_design><study_design>Metabolomics</study_design><study_design>untargeted analysis</study_design><study_design>negative ion mode</study_design><study_design>Reproductive Physiology</study_design><study_design>SIMCA</study_design><study_design>quality control sample</study_design><study_design>Orbitrap Exploris 120</study_design><study_design>CIDR-PGF2alpha</study_design><study_design>electrospray ionization</study_design><study_design>experimental sample</study_design><study_design>Ovis aries</study_design><study_design>Estrus Synchronization</study_design><study_design>UHPLC-MS/MS</study_design><study_design>Kazak ewes</study_design><study_design>XCMS</study_design><study_design>Wuhan Berna Technology Co., Ltd</study_design><study_design>serum</study_design><curator_keywords>Vanquish UHPLC</curator_keywords><curator_keywords>hydrophilic interaction chromatography</curator_keywords><curator_keywords>ProteoWizard msconvert</curator_keywords><curator_keywords>Metabolomics</curator_keywords><curator_keywords>untargeted analysis</curator_keywords><curator_keywords>negative ion mode</curator_keywords><curator_keywords>Reproductive Physiology</curator_keywords><curator_keywords>SIMCA</curator_keywords><curator_keywords>quality control sample</curator_keywords><curator_keywords>Orbitrap Exploris 120</curator_keywords><curator_keywords>CIDR-PGF2alpha</curator_keywords><curator_keywords>electrospray ionization</curator_keywords><curator_keywords>experimental sample</curator_keywords><curator_keywords>Ovis aries</curator_keywords><curator_keywords>Estrus Synchronization</curator_keywords><curator_keywords>UHPLC-MS/MS</curator_keywords><curator_keywords>Kazak ewes</curator_keywords><curator_keywords>XCMS</curator_keywords><curator_keywords>Wuhan Berna Technology Co., Ltd</curator_keywords><curator_keywords>serum</curator_keywords><mass_spectrometry_protocol>&lt;p>Mass spectrometric detection was performed on an Orbitrap Exploris 120 mass spectrometer (Thermo Fisher Scientific) equipped with an electrospray ionization (ESI) source. Data were acquired in both positive and negative ion modes. ESI voltage was set to +3.8 kV in positive mode and -3.4 kV in negative mode. The scan m/z range was 70-1050. Data were collected using the Orbitrap mass analyzer at high resolution.&lt;/p></mass_spectrometry_protocol><metabolite_name>Benzoic acid</metabolite_name><metabolite_name>Dihydroxyacetone</metabolite_name><metabolite_name>Embelin</metabolite_name><metabolite_name>1,6-Anhydro-.beta.-D-glucose</metabolite_name><metabolite_name>Leu-Ile</metabolite_name><metabolite_name>Traumatic acid</metabolite_name><metabolite_name>3-Hydroxyglutaric acid</metabolite_name><metabolite_name>Glycolithocholic acid 3-sulfate</metabolite_name><metabolite_name>Dodecyl gallate</metabolite_name><metabolite_name>Ala-Gly</metabolite_name><metabolite_name>Sunitinib</metabolite_name><metabolite_name>5-Guanidino-2-oxopentanoate</metabolite_name><metabolite_name>2-Ketocaproic acid</metabolite_name><metabolite_name>Succinic_acid_semialdehyde</metabolite_name><metabolite_name>Ketoleucine</metabolite_name><metabolite_name>Phe-Trp</metabolite_name><metabolite_name>Phe-Met-Arg-Phe-amide</metabolite_name><metabolite_name>4,5-DIDEMETHYLSIMMONDSIN</metabolite_name><metabolite_name>alpha-Ketoisovaleric acid</metabolite_name><metabolite_name>Capric acid</metabolite_name><metabolite_name>Ser-Ala</metabolite_name><metabolite_name>Lawsone</metabolite_name><metabolite_name>(3-Methoxy-4-hydroxyphenyl)ethylene_glycol_sulfate</metabolite_name><metabolite_name>(2E)-4-Hydroxybut-2-enoic acid</metabolite_name><metabolite_name>Royal jelly acid</metabolite_name><metabolite_name>Arabinono-1,4-lactone</metabolite_name><metabolite_name>PE(18:0/18:2)</metabolite_name><metabolite_name>Val-Ile</metabolite_name><metabolite_name>Gentisic acid</metabolite_name><metabolite_name>myo-Inositol</metabolite_name><metabolite_name>Pregnanediol 3-O-glucuronide</metabolite_name><metabolite_name>Indoleacetic acid</metabolite_name><metabolite_name>Phosphate</metabolite_name><metabolite_name>2,3-Dihydroxybenzoic acid (Pyrocatechuic acid)</metabolite_name><metabolite_name>2,6-Dihydroxybenzoic acid</metabolite_name><metabolite_name>Thyroxine</metabolite_name><metabolite_name>17.beta.-Estradiol 3-.beta.-D-glucuronide</metabolite_name><metabolite_name>Hydroxyphenyllactic acid</metabolite_name><metabolite_name>Glaucarubin</metabolite_name><metabolite_name>N-Lactoylphenylalanine</metabolite_name><metabolite_name>Taurolithocholic acid</metabolite_name><metabolite_name>Salicylic acid</metabolite_name><metabolite_name>Piperonylic acid</metabolite_name><metabolite_name>3-Methyl-2-oxovaleric acid</metabolite_name><metabolite_name>Xanthine</metabolite_name><metabolite_name>Ethoxyacetic acid</metabolite_name><metabolite_name>Glycylleucine</metabolite_name><metabolite_name>Phloroglucinaldehyde</metabolite_name><metabolite_name>Leu-Trp</metabolite_name><metabolite_name>2,4-Dihydroxybenzoic acid</metabolite_name><metabolite_name>(10E,15Z)-9,12,13-Trihydroxyoctadeca-10,15-dienoic acid</metabolite_name><metabolite_name>Syringic_acid</metabolite_name><metabolite_name>Uracil</metabolite_name><metabolite_name>Hygric acid</metabolite_name><metabolite_name>Lactate</metabolite_name><metabolite_name>cis-​9,​10-​Epoxystearic acid</metabolite_name><metabolite_name>1-Palmitoyl-2-arachidonoyl-sn-glycero-3-phosphoserine</metabolite_name><metabolite_name>5-Hydroxytryptophol (5HTOL)</metabolite_name><metabolite_name>(2-aminoethoxy)[2-[icosa-5.8.11.14-tetraenoyloxy]-3-[octadec-11-enoyloxy]propoxy]phosphinic acid</metabolite_name><metabolite_name>Leu-Val</metabolite_name><metabolite_name>9-Oxo-10(E),12(E)-octadecadienoic acid</metabolite_name><metabolite_name>3-Methoxy-4-hydroxyphenylglycol sulfate</metabolite_name><metabolite_name>Leu-Leu</metabolite_name><metabolite_name>Ethanesulfonic acid</metabolite_name><metabolite_name>Malic acid</metabolite_name><metabolite_name>Daminozide</metabolite_name><metabolite_name>Indoxyl sulfate</metabolite_name><metabolite_name>Ile-Leu</metabolite_name><metabolite_name>Mupirocin</metabolite_name><metabolite_name>2-Arachidonoyl-1-palmitoyl-sn-glycero-3-phosphoethanolamine</metabolite_name><metabolite_name>Chicoric acid</metabolite_name><metabolite_name>Glutamate</metabolite_name><metabolite_name>2-Furoylglycine</metabolite_name><metabolite_name>Oxalic acid</metabolite_name><metabolite_name>5-Sulfosalicylic acid</metabolite_name><metabolite_name>Hydroxymalonate</metabolite_name><metabolite_name>Oxypurinol</metabolite_name><metabolite_name>Pyruvaldehyde</metabolite_name><metabolite_name>osthol</metabolite_name><metabolite_name>arctiin</metabolite_name><metabolite_name>cis-11.14-Eicosadienoic acid</metabolite_name><metabolite_name>Alanylalanine (Ala-Ala)</metabolite_name><metabolite_name>1-Palmitoyllysophosphatidate</metabolite_name><metabolite_name>LPE(18:1(9Z)/0:0)</metabolite_name><metabolite_name>Isopentenyladenine</metabolite_name><metabolite_name>Tiagabine</metabolite_name><metabolite_name>Phenylsulfate</metabolite_name><metabolite_name>Tauro-gamma-muricholic acid</metabolite_name><metabolite_name>alpha-Hydroxyhippuric acid</metabolite_name><metabolite_name>Gly-Ala</metabolite_name><metabolite_name>2-Hydroxybutyric acid</metabolite_name><metabolite_name>cis-Aconitic acid</metabolite_name><metabolite_name>Arachidonic acid (AA)</metabolite_name><metabolite_name>2-Linoleoyl-1-palmitoyl-sn-glycero-3-phosphoethanolamine</metabolite_name><metabolite_name>Pelargonic acid</metabolite_name><metabolite_name>2,2'-Iminodiacetic acid</metabolite_name><metabolite_name>4-Hydroxyphenylacetic acid</metabolite_name><metabolite_name>2-Arachidonoyl-1-stearoyl-sn-glycero-3-phosphoethanolamine</metabolite_name><metabolite_name>3-Hydroxybutyric acid</metabolite_name><metabolite_name>3-Hydroxyphenylacetic acid</metabolite_name></additional><is_claimable>false</is_claimable><name>Serum Metabolomics Reveals Stage-Dependent Metabolic Transitions During CIDR-PGF2alpha-Induced Estrus in Kazak Ewes</name><description>This study investigated serum metabolic transitions during CIDR-PGF2alpha-induced estrus synchronization in Kazak ewes using UHPLC-MS/MS untargeted metabolomics. Eighteen Kazak ewes were assigned to three reproductive stages: luteal phase (LP), luteolysis phase (LDP), and estrus phase (OES), with six animals per group. Serum samples were analyzed by UHPLC-MS/MS on an Orbitrap Exploris 120 instrument using HILIC chromatography (BEH Amide column) in both positive and negative ionization modes. A total of 1,861 metabolites were annotated. Key biomarkers identified include choline, betaine aldehyde, sphingosine, 3-hydroxybutyrylcarnitine, and pregnanediol 3-O-glucuronide, reflecting stage-dependent shifts in phospholipid metabolism, energy utilization, and steroid hormone pathways. This study was funded by NSFC Grant No. 32160770</description><dates><publication>2026-08-09</publication><submission>2026-07-21</submission></dates><accession>MTBLS15117</accession><cross_references><HMDB>HMDB0028716</HMDB><HMDB>HMDB0000562</HMDB><HMDB>HMDB0011738</HMDB><HMDB>HMDB0006695</HMDB><HMDB>HMDB0000194</HMDB><HMDB>HMDB0000064</HMDB><HMDB>HMDB0000097</HMDB><HMDB>HMDB0029154</HMDB><HMDB>HMDB0011171</HMDB><HMDB>HMDB0240311</HMDB><HMDB>HMDB0244237</HMDB><HMDB>HMDB0249243</HMDB><HMDB>HMDB0001252</HMDB><HMDB>HMDB0245980</HMDB><HMDB>HMDB0013127</HMDB><HMDB>HMDB0000252</HMDB><HMDB>HMDB0013222</HMDB><HMDB>HMDB0033971</HMDB><HMDB>HMDB0028813</HMDB><HMDB>HMDB0000050</HMDB><HMDB>HMDB0013751</HMDB><HMDB>HMDB0000992</HMDB><HMDB>HMDB0003157</HMDB><HMDB>HMDB0015411</HMDB><HMDB>HMDB0001924</HMDB><HMDB>HMDB0005036</HMDB><HMDB>HMDB0002169</HMDB><HMDB>HMDB0007921</HMDB><HMDB>HMDB0034198</HMDB><HMDB>HMDB0032545</HMDB><HMDB>HMDB0029586</HMDB><HMDB>HMDB0062312</HMDB><HMDB>HMDB0011152</HMDB><HMDB>HMDB0009093</HMDB><HMDB>HMDB0062308</HMDB><HMDB>HMDB0028964</HMDB><HMDB>HMDB0010400</HMDB><HMDB>HMDB0010389</HMDB><HMDB>HMDB0008539</HMDB><HMDB>HMDB0014958</HMDB><HMDB>HMDB0033633</HMDB><HMDB>HMDB0008244</HMDB><HMDB>HMDB0007003</HMDB><HMDB>HMDB0034117</HMDB><HMDB>HMDB0007006</HMDB><HMDB>HMDB0002096</HMDB><HMDB>HMDB0258715</HMDB><HMDB>HMDB0007007</HMDB><HMDB>HMDB0005800</HMDB><HMDB>HMDB0036018</HMDB><HMDB>HMDB0059571</HMDB><HMDB>HMDB0015383</HMDB><HMDB>HMDB0015213</HMDB><HMDB>HMDB0012305</HMDB><HMDB>HMDB0000593</HMDB><HMDB>HMDB0000564</HMDB><HMDB>HMDB0061712</HMDB><HMDB>HMDB0062559</HMDB><HMDB>HMDB0000791</HMDB><HMDB>HMDB0240609</HMDB><HMDB>HMDB0000201</HMDB><HMDB>HMDB0001185</HMDB><HMDB>HMDB0242112</HMDB><HMDB>HMDB0240766</HMDB><HMDB>HMDB0011760</HMDB><HMDB>HMDB0014380</HMDB><HMDB>HMDB0007994</HMDB><HMDB>HMDB0060370</HMDB><HMDB>HMDB0035945</HMDB><HMDB>HMDB0007956</HMDB><HMDB>HMDB0009251</HMDB><HMDB>HMDB0031896</HMDB><HMDB>HMDB0014758</HMDB><HMDB>HMDB0000086</HMDB><HMDB>HMDB0000848</HMDB><HMDB>HMDB0029659</HMDB><HMDB>HMDB0001545</HMDB><HMDB>HMDB0029660</HMDB><HMDB>HMDB0032469</HMDB><HMDB>HMDB0000323</HMDB><HMDB>HMDB0005066</HMDB><HMDB>HMDB0032604</HMDB><HMDB>HMDB0031654</HMDB><HMDB>HMDB0008443</HMDB><HMDB>HMDB0245307</HMDB><HMDB>HMDB0015652</HMDB><HMDB>HMDB0014643</HMDB><HMDB>HMDB0014524</HMDB><HMDB>HMDB0032878</HMDB><HMDB>HMDB0008165</HMDB><HMDB>HMDB0015269</HMDB><HMDB>HMDB0003559</HMDB><HMDB>HMDB0039229</HMDB><HMDB>HMDB0240205</HMDB><HMDB>HMDB0015232</HMDB><HMDB>HMDB0030803</HMDB><HMDB>HMDB0001043</HMDB><HMDB>HMDB0001895</HMDB><HMDB>HMDB0094696</HMDB><HMDB>HMDB0004669</HMDB><HMDB>HMDB0000759</HMDB><HMDB>HMDB0007853</HMDB><HMDB>HMDB0001855</HMDB><HMDB>HMDB0013676</HMDB><HMDB>HMDB0001429</HMDB><HMDB>HMDB0000211</HMDB><HMDB>HMDB0251767</HMDB><HMDB>HMDB0000933</HMDB><HMDB>HMDB0000722</HMDB><HMDB>HMDB0000847</HMDB><HMDB>HMDB0010318</HMDB><HMDB>HMDB0002329</HMDB><HMDB>HMDB0000248</HMDB><HMDB>HMDB0000397</HMDB><HMDB>HMDB0029032</HMDB><HMDB>HMDB0000292</HMDB><HMDB>HMDB0000300</HMDB><HMDB>HMDB0000439</HMDB><HMDB>HMDB0001900</HMDB><HMDB>HMDB0003332</HMDB><HMDB>HMDB0000440</HMDB><HMDB>HMDB0028932</HMDB><HMDB>HMDB0029006</HMDB><HMDB>HMDB0038720</HMDB><HMDB>HMDB0028942</HMDB><HMDB>HMDB0000020</HMDB><HMDB>HMDB0029130</HMDB><HMDB>HMDB0003459</HMDB><HMDB>HMDB0125090</HMDB><HMDB>HMDB0000152</HMDB><HMDB>HMDB0028911</HMDB><HMDB>HMDB0144295</HMDB><HMDB>HMDB0028933</HMDB><HMDB>HMDB0001870</HMDB><HMDB>HMDB0000786</HMDB><HMDB>HMDB0006899</HMDB><HMDB>HMDB0029666</HMDB><HMDB>HMDB0001882</HMDB><HMDB>HMDB0252875</HMDB><HMDB>HMDB0244269</HMDB><HMDB>HMDB0250838</HMDB><HMDB>HMDB0000932</HMDB><HMDB>HMDB0002404</HMDB><HMDB>HMDB0015397</HMDB><HMDB>HMDB0001259</HMDB><HMDB>HMDB0014554</HMDB><HMDB>HMDB0011753</HMDB><HMDB>HMDB0031212</HMDB><HMDB>HMDB0000559</HMDB><HMDB>HMDB0028940</HMDB><HMDB>HMDB0000428</HMDB><HMDB>HMDB0000640</HMDB><HMDB>HMDB0003381</HMDB><HMDB>HMDB0252425</HMDB><HMDB>HMDB0012361</HMDB><HMDB>HMDB0041207</HMDB><HMDB>HMDB0035626</HMDB><HMDB>HMDB0002375</HMDB><HMDB>HMDB0301809</HMDB><HMDB>HMDB0015042</HMDB><HMDB>HMDB0302150</HMDB><HMDB>HMDB0252003</HMDB><HMDB>HMDB0004225</HMDB><HMDB>HMDB0000491</HMDB><HMDB>HMDB0001864</HMDB><HMDB>HMDB0000695</HMDB><HMDB>HMDB0011506</HMDB><HMDB>HMDB0247617</HMDB><HMDB>HMDB0000008</HMDB><HMDB>HMDB0001167</HMDB><HMDB>HMDB0032613</HMDB><HMDB>HMDB0008928</HMDB><HMDB>HMDB0002639</HMDB><HMDB>HMDB0253997</HMDB><HMDB>HMDB0035919</HMDB><HMDB>HMDB0008937</HMDB><HMDB>HMDB0009036</HMDB><HMDB>HMDB0000072</HMDB><HMDB>HMDB0005060</HMDB><HMDB>HMDB0000148</HMDB><HMDB>HMDB0000744</HMDB><HMDB>HMDB0000019</HMDB><HMDB>HMDB0000682</HMDB><HMDB>HMDB0000755</HMDB><HMDB>HMDB0000511</HMDB><HMDB>HMDB0060015</HMDB><HMDB>HMDB0000011</HMDB><HMDB>HMDB0000197</HMDB><HMDB>HMDB0062175</HMDB><HMDB>HMDB0008994</HMDB><HMDB>HMDB0009003</HMDB><HMDB>HMDB0002085</HMDB><HMDB>HMDB0245646</HMDB><HMDB>HMDB0011725</HMDB><HMDB>HMDB0006224</HMDB><HMDB>HMDB0035227</HMDB><KEGG>C19809</KEGG></cross_references></HashMap>