Summary of Study ST003042

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001893. The data can be accessed directly via it's Project DOI: 10.21228/M81F0P This work is supported by NIH grant, U2C- DK119886.

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This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST003042
Study TitleThe metabolomic resetting effect of DY131 in cisplatin-induced AKI
Study TypeMS
Study SummaryLC-MS/MS analyses were performed using renal tissues from cisplatin-induced AKI mice with or without DY131 treatment. The data revealed that DY131 alleviated cisplatin-induced mitochondrial dysfunction and energy metabolism disorder, as well as multiple metabolic disorders.
Institute
Children's Hospital of Nanjing Medical University
DepartmentDepartment of Nephrology, State Key Laboratory of Reproductive Medicine
LaboratoryNanjing Key Lab of Pediatrics, Jiangsu Key Laboratory of Pediatrics
Last NameLu
First NameLingling
AddressGuangzhou Road 72, Nanjing, Jiangsu, 210000, China
Emaillulingling89tara@163.com
Phone0086-25-8311-7435
Submit Date2023-12-21
Raw Data AvailableYes
Raw Data File Type(s)mzXML
Analysis Type DetailLC-MS
Release Date2024-02-08
Release Version1
Lingling Lu Lingling Lu
https://dx.doi.org/10.21228/M81F0P
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001893
Project DOI:doi: 10.21228/M81F0P
Project Title:The metabolomic resetting effect of DY131 in cisplatin-induced AKI
Project Type:MS quantitative analysis
Project Summary:Acute kidney injury (AKI) remains a challenge in clinical practice, and mitochondrial injury is a hallmark of AKI independent of the exact aetiology. ERRγ is a member of orphan nuclear receptors which plays a regulatory role in mitochondrial biosynthesis, energy metabolism, oxidative stress, cell apoptosis, inflammation, and especially metabolic pathways. Here we investigate the role of pharmacological agonist of ERRγ, DY131, in AKI mice induced by cisplatin, IR and LPS. DY131 ameliorated renal function, tubular injury, cell apoptosis and inflammation in AKI mice with multiple causes. Furthermore, we performed LC-MS/MS analyses using renal tissues from cisplatin-induced AKI mice with or without DY131 treatment. Strikingly, the data revealed that DY131 alleviated cisplatin-induced mitochondrial dysfunction and energy metabolism disorder, as well as multiple metabolic disorders. Taken together, the findings highlighted the protective effect of DY131 on AKI probably via improving mitochondrial function and energy metabolism.
Institute:Children's Hospital of Nanjing Medical University
Department:Department of Nephrology, State Key Laboratory of Reproductive Medicine
Laboratory:Nanjing Key Lab of Pediatrics, Jiangsu Key Laboratory of Pediatrics
Last Name:Lu
First Name:Lingling
Address:Guangzhou Road 72, Nanjing, Jiangsu, 210000, China
Email:lulingling89tara@163.com
Phone:0086-25-8311-7435

Subject:

Subject ID:SU003157
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:C57BL/6J
Age Or Age Range:7-8 weeks
Weight Or Weight Range:20-25g
Gender:Male
Animal Animal Supplier:Nanjing Medical University
Animal Housing:Nanjing Medical University
Animal Feed:Free to food
Animal Water:Free to clean water

Factors:

Subject type: Mammal; Subject species: Mus musculus (Factor headings shown in green)

mb_sample_id local_sample_id Treatment
SA330375C_4control
SA330376C_3control
SA330377C_5control
SA330378C_6control
SA330379C_7control
SA330380C_1control
SA330381C_2control
SA330368DY_P_5DY131+cisplatin
SA330369DY_P_6DY131+cisplatin
SA330370DY_P_4DY131+cisplatin
SA330371DY_P_3DY131+cisplatin
SA330372DY_P_1DY131+cisplatin
SA330373DY_P_7DY131+cisplatin
SA330374DY_P_2DY131+cisplatin
SA330382P_4vehicle+cisplatin
SA330383P_2vehicle+cisplatin
SA330384P_1vehicle+cisplatin
SA330385P_3vehicle+cisplatin
SA330386P_5vehicle+cisplatin
SA330387P_6vehicle+cisplatin
SA330388P_7vehicle+cisplatin
Showing results 1 to 21 of 21

Collection:

Collection ID:CO003150
Collection Summary:The mice were euthanized 72 hours after cisplatin injection, and renal tissues were collected and frozen at -80℃.
Sample Type:Kidney
Storage Conditions:-80℃

Treatment:

Treatment ID:TR003166
Treatment Summary:Wild type C57BL/6J mice were maintained under standard environmental conditions. A single injection of cisplatin (25 mg/kg, i.p.) was used to induce AKI. DY131 was dissolved in DMSO and further diluted with 5% Tween-80. To assess the effect of DY131, the mice were injected with DY131 (5 mg/kg, i.p.) or vehicle one hour before cisplatin injection, repeated every 24 hours. The mice were euthanized 72 hours after cisplatin injection.
Treatment Compound:cisplatin or saline, DY131 or vehicle
Treatment Route:intraperitoneal injection ​
Treatment Dose:cisplatin at 25 mg/kg, once. DY131 at 5 mg/kg, once a day for 3 days
Treatment Dosevolume:Animal Vet Treatments: Animal Anesthesia: Animal Acclimation Duration: Animal Fasting: Animal Endpoint Euthanasia: Animal Endpoint Tissue Coll. List: Animal Endpoint Tissue Proc. Method: Animal Endpoint Clinical Signs:
Treatment Vehicle:cisplatin dissolved in saline, DY131 dissolved in DMSO and further diluted with 5% Tween-80

Sample Preparation:

Sampleprep ID:SP003163
Sampleprep Summary:25 mg of sample was weighted to an EP tube, and 500 μL extract solution (acetonitrile: methanol: water = 2: 2: 1, with isotopically-labelled internal standard mixture) was added. After 30 s vortex, the samples were homogenized at 35 Hz for 4 min and sonicated for 5 min in ice-water bath. The homogenization and sonication cycle was repeated for 3 times. Then the samples were incubated for 1 h at -40 ℃ and centrifuged at 12000 rpm for 15 min at 4 ℃. The resulting supernatant was transferred to a fresh glass vial for analysis.

Combined analysis:

Analysis ID AN004990 AN004991
Analysis type MS MS
Chromatography type HILIC HILIC
Chromatography system Thermo Fisher Scientific Thermo Fisher Scientific
Column Waters ACQUITY UPLC BEH Amide (100 x 2.1mm,1.7um) Waters ACQUITY UPLC BEH Amide (100 x 2.1mm,1.7um)
MS Type ESI ESI
MS instrument type Orbitrap Orbitrap
MS instrument name Thermo Q Exactive HF-X Orbitrap Thermo Q Exactive HF-X Orbitrap
Ion Mode POSITIVE NEGATIVE
Units Peak area Peak area

Chromatography:

Chromatography ID:CH003770
Methods Filename:DY131_Chromatography.txt
Instrument Name:Thermo Fisher Scientific
Column Name:Waters ACQUITY UPLC BEH Amide (100 x 2.1mm,1.7um)
Column Temperature:30 ℃
Flow Gradient:0-0.5min, 95% B; 0.5-7min, 95%-65%B; 7-8min, 65%B-40%B; 8-9min, 40%B; 9-9.1min, 40%-95%B; 9.1-12min, 95%B
Flow Rate:0.5ml/min
Solvent A:water(pH = 9.75)
Solvent B:acetonitrile
Chromatography Type:HILIC

MS:

MS ID:MS004730
Analysis ID:AN004990
Instrument Name:Thermo Q Exactive HF-X Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:sheath gas flow rate as 30 Arb, Aux gas flow rate as 25 Arb, capillary temperature 350 ℃, full MS resolution as 60000, MS/MS resolution as 7500, collision energy as 10/30/60 in NCE mode, spray Voltage as 3.6 kV (positive). Metabolites were quantified by relative quantification and expressed by peak area.
Ion Mode:POSITIVE
Analysis Protocol File:DY131_MS.txt
  
MS ID:MS004731
Analysis ID:AN004991
Instrument Name:Thermo Q Exactive HF-X Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:sheath gas flow rate as 30 Arb, Aux gas flow rate as 25 Arb, capillary temperature 350 ℃, full MS resolution as 60000, MS/MS resolution as 7500, collision energy as 10/30/60 in NCE mode, spray Voltage as -3.2 kV (negative). Metabolites were quantified by relative quantification and expressed by peak area.
Ion Mode:NEGATIVE
Analysis Protocol File:DY131_MS.txt
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