Summary of Study ST003746

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 PR002332. The data can be accessed directly via it's Project DOI: 10.21228/M86C29 This work is supported by NIH grant, U2C- DK119886. See: https://www.metabolomicsworkbench.org/about/howtocite.php

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Study IDST003746
Study TitleSerum hormone-targeted metabolome of sleep-deprived mice
Study SummarySleep disturbances associate with pathogenesis of numerous chronic disorders, including chronic gastrointestinal diseases. However, the mechanism that transmits sleep disturbance-induced aberrant neural signaling from the brain to the gut remains elusive. We show that acute sleep deprivation (SD) impairs intestinal stem cell function, leading to shortening of crypt-villus architecture and Paneth cell loss. We identified dorsal motor nucleus of vagus (DMV) as the SD-sensitive central nervous system center that transmits sleep effects to the gut. SD aberrantly activates DMV neurons, driving excessive acetylcholine release from the vagus nerve into the gut. Acetylcholine triggers 5-hydroxytryptamine (5-HT) release by enterochromaffin cells and suppresses its reuptake via muscarinic receptors, thereby causing a spike in 5-HT levels. Elevated 5-HT induces excessive oxidative stress in intestinal stem cells through its receptor HTR4, promoting gut pathologies. Overall, we reveal SD-responsive neural circuit that controls intestinal stem cells and identify therapeutic strategies for mitigating SD-related gut diseases.
Institute
China Agricultural University
Last NameZhang
First NameMingxin
Address2 West Yuanmingyuan Road, Beijing, Beijing, 100193, China
Emailzmx15310686122@163.com
Phone18800152903
Submit Date2025-02-14
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2026-01-02
Release Version1
Mingxin Zhang Mingxin Zhang
https://dx.doi.org/10.21228/M86C29
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR002332
Project DOI:doi: 10.21228/M86C29
Project Title:Serum hormone-targeted metabolome of sleep-deprived mice
Project Summary:This project investigates the changes in serum hormone levels before and after 2 days of sleep deprivation in mice, exploring the alterations in serum hormone release caused by sleep deprivation. Metabolomic results indicate that in mice subjected to 2 days of sleep deprivation, serum hormones such as DHT, Progesterone, and Corticosterone were significantly reduced
Institute:China Agriculture University
Last Name:Zhang
First Name:Mingxin
Address:2 West Yuanmingyuan Road, Beijing, Beijing, 100193, China
Email:zmx15310686122@163.com
Phone:18800152903

Subject:

Subject ID:SU003879
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090

Factors:

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

mb_sample_id local_sample_id Treatment
SA408229SD0d_1Ctrl
SA408230SD0d_2Ctrl
SA408231SD0d_3Ctrl
SA408232SD0d_4Ctrl
SA408233SD0d_5Ctrl
SA408234SD2d_1SD2d
SA408235SD2d_2SD2d
SA408236SD2d_3SD2d
SA408237SD2d_4SD2d
SA408238SD2d_5SD2d
Showing results 1 to 10 of 10

Collection:

Collection ID:CO003872
Collection Summary:Fresh blood from mice was collected via cardiac puncture before and after 48 hours of continuous sleep deprivation. After allowing the blood to stand for 1 hour, it was centrifuged at 3000g for 10 minutes to obtain serum. A total of 100 μL of serum sample was collected.
Sample Type:Blood (serum)

Treatment:

Treatment ID:TR003888
Treatment Summary:The serum sample was mixed by adding 100 μL of methanol, and then 100 μL of water was added and mixed at 4°C. The samples were centrifuged at 12000 rpm for 15 min.

Sample Preparation:

Sampleprep ID:SP003885
Sampleprep Summary:The supernatant obtained after centrifugation was removed and slowly passed through the Oasis PRIME HLB column. The column was washed with 5% methanol. Finally, the animal hormones were eluted using 90/10 (v/v) acetonitrile/methanol and collected. The eluate was dried and redissolved before injection for LC-MS analysis.

Combined analysis:

Analysis ID AN006152
Chromatography ID CH004673
MS ID MS005857
Analysis type MS
Chromatography type HILIC
Chromatography system AB Sciex QTRAP 6500+
Column Kinetex C18 column (100 x 2.1 mm, 2.6 μm)
MS Type ESI
MS instrument type QTOF
MS instrument name Agilent 6520 QTOF
Ion Mode POSITIVE
Units ng/mL

Chromatography:

Chromatography ID:CH004673
Instrument Name:AB Sciex QTRAP 6500+
Column Name:Kinetex C18 column (100 x 2.1 mm, 2.6 μm)
Column Temperature:45°C
Flow Gradient:initial 5% B, 2min; 5-40% B, 4min; 40-70% B, 7 min; 70-100% B, 7.5min; 100% B, 9min; 100-5% B, 9.1min; 5% B, 11min.
Flow Rate:0.30 mL/min
Solvent A:100% Water; 0.1% Formic acid; 5mM Ammonium acetate
Solvent B:100% Acetonitrile; 0.1% Formic acid
Chromatography Type:HILIC

MS:

MS ID:MS005857
Analysis ID:AN006152
Instrument Name:Agilent 6520 QTOF
Instrument Type:QTOF
MS Type:ESI
MS Comments:Curtain Gas:35psi; Collision Gas:Medium;IonSpray Voltage:4500V; Temperature:550℃; Ion Source Gas 1:60; Ion Source Gas 2:60 The characteristic ion of each substance is screened by the triple quadrupole, and the signal of the characteristic ion is obtained in the detector No. Intensity (CPS), open the sample mass spectrometry file with SCIEX OS V1.4 software, and perform chromatographic peaks Integration and calibration work, the peak Area (Area) of each chromatographic peak represents the relative quantitative value of the corresponding substance, the most All chromatographic peak area integral data were then exported
Ion Mode:POSITIVE
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