Summary of Study ST002522

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 PR001624. The data can be accessed directly via it's Project DOI: 10.21228/M8S99J 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 IDST002522
Study TitleLipidomics study on the effect of LBP protein on hepatic lipid composition in mice
Study SummaryStress elevates the formation of ROS and lipid peroxidation, which induce lipid droplets (LDs) accumulation and adverse metabolic disturbance. Here, we explored the novel role of Lipopolysaccharide-binding protein (LBP) as an anti-oxidant, which can capture unsaturated triglyceride (TG) into LDs to avoid lipid peroxidation. Oxidative stress upregulates LBP level and promotes LDs growth via the LBP/TG phase transition. Upon N-Acetyl-L-cysteine (NAC) elimination of ROS, LBP is exported from LD along with PRDX4, resulting in an increase in phospholipid synthesis. Chronic stress causes LBP upregulation and leads to obesity, which can be rescued by NAC treatment in vivo. These results support that LBP maintains homeostasis by coupling lipid metabolism and redox signal, which provides insights into redox medicine that mitigate stress-induced metabolic dysfunction. Hepatic lipidomics in overexpressed LBP and WT mice treated with NAC after 24h fasting
Institute
University of Science and Technology of China
DepartmentDepartment of Endocrinology and Laboratory for Diabetes
LaboratoryThe First Affiliated Hospital of USTC, Division of Life Sciences and Medicine
Last NameZhang
First NameQilun
AddressLujiang road no.17
Emailzql66666@mail.ustc.edu.cn
Phone+8618356507293
Submit Date2023-03-21
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Analysis Type DetailLC-MS
Release Date2024-03-21
Release Version1
Qilun Zhang Qilun Zhang
https://dx.doi.org/10.21228/M8S99J
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

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

mb_sample_id local_sample_id Genotype Treatment
SA254474KIHFD3LBPKI/KI HFD16W
SA254475KIHFD2LBPKI/KI HFD16W
SA254476KIHFD1LBPKI/KI HFD16W
SA254477KIND2LBPKI/KI ND
SA254478KIND1LBPKI/KI ND
SA254479KIND3LBPKI/KI ND
SA254480WTFAST2Wild-type FAST24H
SA254481WTFAST1Wild-type FAST24H
SA254482WTFAST3Wild-type FAST24H
SA254483WTFASTNAC1Wild-type FAST24HNAC3H
SA254484WTFASTNAC2Wild-type FAST24HNAC3H
SA254485WTFASTNAC3Wild-type FAST24HNAC3H
SA254486WTHFD1Wild-type HFD16W
SA254487WTHFD2Wild-type HFD16W
SA254488WTHFD3Wild-type HFD16W
SA254489WTND2Wild-type ND
SA254490WTND3Wild-type ND
SA254491WTND1Wild-type ND
Showing results 1 to 18 of 18
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