Summary of Study ST003469

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 PR002122. The data can be accessed directly via it's Project DOI: 10.21228/M8B52G This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

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.

Study ID	ST003469
Study Title	Lipidomics of mice white adipose tissue to support understanding of early metabolic shift in presymptomatic sepsis patients. (Part14 mice white adipose tissue lipid)
Study Summary	Sepsis, a life-threatening organ dysfunction caused by a dysregulated response to infection, is a critical medical condition with significant global impact, responsible for 48.9 million cases and 11 million deaths annually. Metabolic dysregulation in sepsis is a critical determinant of disease outcome, yet most studies focus on patients after severe illness onset, comparing septic versus non-septic groups or survivors versus non-survivors. To truly understand this complex disease, it is essential to investigate early metabolic shifts, capturing the transition from simple infection to sepsis. Our untargeted lipidome analysis of white adipose tissue from mice model revealed early septic biomarkers in white adipose tissue.
Institute	Leibniz Institute for Natural Product Research and Infection Biology Hans Knöll Institute
Department	Microbiome Dynamics
Last Name	XU
First Name	LINLIN
Address	Beutenbergstraße 11a, Jena, Thuringia, 07745, Germany
Email	Lin-Lin.Xu@hki-jena.de
Phone	+4936415321265
Submit Date	2024-09-05
Raw Data Available	Yes
Raw Data File Type(s)	mzML
Analysis Type Detail	LC-MS
Release Date	2025-05-26
Release Version	1

Select appropriate tab below to view additional metadata details:

Project:

Project ID:	PR002122
Project DOI:	doi: 10.21228/M8B52G
Project Title:	Early Metabolic Shifts in the Sepsis: Insights from Presymptomatic Patients and In Vivo Models.
Project Type:	MS quantitative analysis
Project Summary:	Metabolomics of human serum to support understanding of early metabolic shift in presymptomatic sepsis patients and further confirmed in in vivo model.
Institute:	Leibniz Institute for Natural Product Research and Infection Biology Hans Knöll Institute
Department:	Microbiome Dynamics
Last Name:	XU
First Name:	LINLIN
Address:	Beutenbergstraße 11a, Jena, Thuringia, 07745, Germany
Email:	Lin-Lin.Xu@leibniz-hki.de
Phone:	+4936415321265

Subject:

Subject ID:	SU003597
Subject Type:	Mammal
Subject Species:	Mus musculus
Taxonomy ID:	10090
Gender:	Not applicable
Species Group:	Mammals

Factors:

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

mb_sample_id	local_sample_id	Sample source	Group
SA383080	Blank_004	blank	Blank
SA383081	Blank_PB	blank	Blank
SA383082	Blank_001	blank	Blank
SA383083	Blank_002	blank	Blank
SA383084	Blank_003	blank	Blank
SA383051	SA020986	White adipose tissue	CLP (24h) / 12C-Serin
SA383052	SA020979	White adipose tissue	CLP (24h) / 12C-Serin
SA383053	SA021021	White adipose tissue	CLP (24h) / 12C-Serin
SA383054	SA021028	White adipose tissue	CLP (24h) / 12C-Serin
SA383055	SA020944	White adipose tissue	CLP (24h) / 13C-Serin
SA383056	SA020891	White adipose tissue	CLP (24h) / 13C-Serin
SA383057	SA020937	White adipose tissue	CLP (24h) / 13C-Serin
SA383058	SA020884	White adipose tissue	CLP (24h) / 13C-Serin
SA383059	SA020926	White adipose tissue	CLP (24h) / Vehicle
SA383060	SA020898	White adipose tissue	CLP (24h) / Vehicle
SA383061	SA020972	White adipose tissue	CLP (24h) / Vehicle
SA383062	QC_001	White adipose tissue	QC
SA383063	QC_009	White adipose tissue	QC
SA383064	QC_004	White adipose tissue	QC
SA383065	QC_008	White adipose tissue	QC
SA383066	QC_006	White adipose tissue	QC
SA383067	QC_007	White adipose tissue	QC
SA383068	QC_005	White adipose tissue	QC
SA383069	SA021014	White adipose tissue	Sham / 12C-Serin
SA383070	SA021000	White adipose tissue	Sham / 12C-Serin
SA383071	SA021007	White adipose tissue	Sham / 12C-Serin
SA383072	SA020993	White adipose tissue	Sham / 12C-Serin
SA383073	SA020905	White adipose tissue	Sham / 13C-Serin
SA383074	SA020965	White adipose tissue	Sham / 13C-Serin
SA383075	SA020958	White adipose tissue	Sham / 13C-Serin
SA383076	SA020912	White adipose tissue	Sham / 13C-Serin
SA383077	SA020951	White adipose tissue	Sham / Vehicle
SA383078	SA020919	White adipose tissue	Sham / Vehicle
SA383079	SA020931	White adipose tissue	Sham / Vehicle

Showing results 1 to 34 of 34

Showing results 1 to 34 of 34

Collection:

Collection ID:	CO003590
Collection Summary:	Mice tissue samples were collected from our in vivo mice model and frozen at -80 °C. Samples were shipped to MS-OMICS for metabolomic analysis.
Sample Type:	White adipose

Treatment:

Treatment ID:	TR003606
Treatment Summary:	Approximately 30% of the cecum was ligated and punctured twice with a 23 Gauge (G) needle. A small amount of faeces was extruded and the cecum was placed back into the abdominal cavity. All animals received 40 mL/kg saline s.c. directly after the procedure and once 25mg/kg s.c. Imipenem/Cilastatin after 6 hours. This model is associated with a 14-day mortality of 30%, closely mimicking the clinical situation. Animals were orally gavaged with 500mg/kg 12C-Serin (Sigma) or 13C-Serin (CLM-1574-H-0.25 Serine-L (13C3 99%13C), Euroisotope, Germany) in 10mL/kg drinking water or drinking water only (vehicle) 6 and 18 hours after CLP98,99. After 24 hours, the animals are then perfused with ice cold PBS and organs were harvested, snap frozen and stored at -80° until further analysis. Sham animals underwent exactly to the same procedures except for the CLP.

Treatment ID:

TR003606

Treatment Summary:

Approximately 30% of the cecum was ligated and punctured twice with a 23 Gauge (G) needle. A small amount of faeces was extruded and the cecum was placed back into the abdominal cavity. All animals received 40 mL/kg saline s.c. directly after the procedure and once 25mg/kg s.c. Imipenem/Cilastatin after 6 hours. This model is associated with a 14-day mortality of 30%, closely mimicking the clinical situation. Animals were orally gavaged with 500mg/kg 12C-Serin (Sigma) or 13C-Serin (CLM-1574-H-0.25 Serine-L (13C3 99%13C), Euroisotope, Germany) in 10mL/kg drinking water or drinking water only (vehicle) 6 and 18 hours after CLP98,99. After 24 hours, the animals are then perfused with ice cold PBS and organs were harvested, snap frozen and stored at -80° until further analysis. Sham animals underwent exactly to the same procedures except for the CLP.

Sample Preparation:

Sampleprep ID:	SP003604
Sampleprep Summary:	In the different tissue samples, the pellet from the semipolar extraction were used to extract lipids as follows. DCM:MeOH (3:1) were added to the pellets, and the samples were homogenized using a pre-cooled Bead-beater (4 x 60 sec at 30 Hz), with colling of the blocks between the beading cycles. Subsequently, the samples were ultrasonicate for 5 mins and centrifuged (5 mins, 1800 RCF, 4 °C). The supernatant were collected and dried under nitrogen gas. Samples were then reconstitute with 6x (spleen and WAT) or 3x (heart, liver and kidney) the sample weight with the reconstitution solvent eluent mix and vortex mixed for 30 sec. The reconstituted samples were filtrated using SpinX filters by centrifugation (5 mins, 1800 RCF, 4 °C). All samples were mixed 1: 50 in eluent mix. For serum samples, an alliqoute of the serum samples are mixed with extraction solvent (0.1 M BHT in isopropanol with stable isotope labelled internal standard) in a Spin-X® filter. The filters were vortex-mixed for 60 sec and left at room temperature for 10 mins before placing in -20 °C Freezer overnight. The following day samples were left at room temperature for 30 mins before centrifuging (1800g /4°C/2 min). The filtrate were mixed with eluent mix 1:3.

Sampleprep ID:

SP003604

Sampleprep Summary:

In the different tissue samples, the pellet from the semipolar extraction were used to extract lipids as follows. DCM:MeOH (3:1) were added to the pellets, and the samples were homogenized using a pre-cooled Bead-beater (4 x 60 sec at 30 Hz), with colling of the blocks between the beading cycles. Subsequently, the samples were ultrasonicate for 5 mins and centrifuged (5 mins, 1800 RCF, 4 °C). The supernatant were collected and dried under nitrogen gas. Samples were then reconstitute with 6x (spleen and WAT) or 3x (heart, liver and kidney) the sample weight with the reconstitution solvent eluent mix and vortex mixed for 30 sec. The reconstituted samples were filtrated using SpinX filters by centrifugation (5 mins, 1800 RCF, 4 °C). All samples were mixed 1: 50 in eluent mix. For serum samples, an alliqoute of the serum samples are mixed with extraction solvent (0.1 M BHT in isopropanol with stable isotope labelled internal standard) in a Spin-X® filter. The filters were vortex-mixed for 60 sec and left at room temperature for 10 mins before placing in -20 °C Freezer overnight. The following day samples were left at room temperature for 30 mins before centrifuging (1800g /4°C/2 min). The filtrate were mixed with eluent mix 1:3.

Chromatography:

Chromatography ID:	CH004326
Methods Filename:	Doneanu_etal.pdf
Instrument Name:	Thermo Vanquish
Column Name:	Waters ACQUITY UPLC CSH C18 (100 x 2.1mm,1.7um)
Column Temperature:	55
Flow Gradient:	0-2 min: 40 % B, 2.1 min 50% B, 12 min 54% B, 12.1 min 70% B, 18-20 min 99 % B, 20.1-22 min 40% B
Flow Rate:	0.4mL/min
Solvent A:	60% Acetonitrile/40% water; 10 mM ammonium formate; 0.1% formic acid
Solvent B:	90% Isopropanol/10% acetonitrile; 10 mM ammonium formate; 0.1% formic acid
Chromatography Type:	Reversed phase

Analysis:

Analysis ID:	AN005703
Laboratory Name:	MS-Omics, Denmark
Analysis Type:	MS
Analysis Protocol File:	Doneanu_etal.pdf
Chromatography ID:	CH004326
Num Factors:	8
Num Metabolites:	146
Has Rt:	1
Rt Units:	Minutes
Results File:	ST003469_AN005703_Results.txt
Units:	Normalized peak area

Analysis ID:	AN005704
Laboratory Name:	MS-Omics, Denmark
Analysis Type:	MS
Analysis Protocol File:	Doneanu_etal.pdf
Chromatography ID:	CH004326
Num Factors:	8
Num Metabolites:	55
Has Rt:	1
Rt Units:	Minutes
Results File:	ST003469_AN005704_Results.txt
Units:	Normalized peak area