Summary of Study ST003739

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 PR002325. The data can be accessed directly via it's Project DOI: 10.21228/M83J9R This work is supported by NIH grant, U2C- DK119886. See: https://www.metabolomicsworkbench.org/about/howtocite.php

Perform statistical analysis  |  Show all samples  |  Show named metabolites  |  Download named metabolite data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST003739
Study TitleSerum neurotransmitter targeted metabolome in sleep-deprived (SD) 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/M83J9R
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR002325
Project DOI:doi: 10.21228/M83J9R
Project Title:Serum neurotransmitter targeted metabolome in sleep-deprived mice
Project Summary:This project investigates the changes in serum neurotransmitter levels before and after 2 days of sleep deprivation in mice, exploring the alterations in serum neurotransmitter release caused by sleep deprivation. Metabolomic results indicate that in mice subjected to 2 days of sleep deprivation, serum neurotransmitters such as 5-HTP, Kyn, and KynA were significantly reduced, while Ach, Gln, Trp, and 5-HT were significantly increased.
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:SU003871
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Gender:Female

Factors:

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

mb_sample_id local_sample_id Treatment
SA407853SD0d_1Ctrl
SA407854SD0d_2Ctrl
SA407855SD0d_3Ctrl
SA407856SD0d_4Ctrl
SA407857SD0d_5Ctrl
SA407858SD2d_1SD2d
SA407859SD2d_2SD2d
SA407860SD2d_3SD2d
SA407861SD2d_4SD2d
SA407862SD2d_5SD2d
Showing results 1 to 10 of 10

Collection:

Collection ID:CO003864
Collection Summary:Serum samples were obtained immediately after mice were subjected to 48 hours of continuous sleep deprivation(SD). Fresh blood from mice was collected via cardiac puncture before and after sleep deprivation. After allowing the blood to stand for 1 hour, it was centrifuged at 3000g for 10 minutes to obtain 400 µL of serum, which was then stored at -80°C.
Sample Type:Blood (serum)

Treatment:

Treatment ID:TR003880
Treatment Summary:The samples (100 μL for each sample) were homogenized with 200 μL of acetonitrile (80%) which contained mixed internal standards and centrifuged at 12,000 rpm for 10 min. Finally, the supernatant (2 μL) was injected into the LC-MS/MS system for analysis.

Sample Preparation:

Sampleprep ID:SP003877
Sampleprep Summary:The stock solution of individual neurotransmitter was mixed and prepared in neurotransmitter-free matrix to obtain a series of neurotransmitter calibrators. Certain concentrations of L-Tyrosine-d4 was mixed as Internal Standard (IS). The stock solution of all of these and working solution were stored in refrigerator of -20°C

Combined analysis:

Analysis ID AN006139
Chromatography ID CH004663
MS ID MS005845
Analysis type MS
Chromatography type HILIC
Chromatography system AB Sciex QTRAP 6500+
Column Waters XSelect HSS T3 XP (150 x 3mm,2.5um)
MS Type ESI
MS instrument type QTOF
MS instrument name Agilent 6520 QTOF
Ion Mode POSITIVE
Units ng/ml

Chromatography:

Chromatography ID:CH004663
Instrument Name:AB Sciex QTRAP 6500+
Column Name:Waters XSelect HSS T3 XP (150 x 3mm,2.5um)
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:MS005845
Analysis ID:AN006139
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
Ion Mode:POSITIVE
  logo