TY - JOUR
T1 - GC/MS-based urinary metabolomics reveals systematic differences in metabolism and ethanol response between Sprague-Dawley and Wistar rats
AU - Gao, Xianfu
AU - Zhao, Aihua
AU - Zhou, Mingmei
AU - Lin, Jingchao
AU - Qiu, Yunping
AU - Su, Mingming
AU - Jia, Wei
N1 - Funding Information:
Acknowledgments This work was financially supported by the projects of Shanghai Commission of Science and Technology (07DZ19715), and National comprehensive technology platforms for innovative drug R&D (2009ZX09301-007) and E-institutes of Shanghai Municipal Education Comminssion, Project Number: E03008, 09YZ119.
PY - 2011/9
Y1 - 2011/9
N2 - Metabolic differences of experimental animals contribute to pharmacological variations. Sprague-Dawley (SD) and Wistar rats are commonly used experimental rats with similar genetic background, and considered interchangeable in practical researches. In this study, we present the urinary metabolomics results, based on gas chromatography coupled to mass spectrometry (GC/MS), which reveal the systematic metabolic differences between SD and Wistar rats under different perturbations such as fasting, feeding, and consecutive acute ethanol interventions. The different metabotypes between the two strains of rats involve a number of metabolic pathways and symbiotic gut microflora. SD rats exhibited higher individualized metabolic variations in the fasting and feeding states, and a stronger ability to recover from an altered metabolic profile with less hepatic injury from the consecutive ethanol exposure, as compared to Wistar rats. In summary, the GC/MS-based urinary metabolomics studies demonstrated an intrinsic metabolic difference between SD and Wistar rats, which warrants consideration in experimental design using these animal strains.
AB - Metabolic differences of experimental animals contribute to pharmacological variations. Sprague-Dawley (SD) and Wistar rats are commonly used experimental rats with similar genetic background, and considered interchangeable in practical researches. In this study, we present the urinary metabolomics results, based on gas chromatography coupled to mass spectrometry (GC/MS), which reveal the systematic metabolic differences between SD and Wistar rats under different perturbations such as fasting, feeding, and consecutive acute ethanol interventions. The different metabotypes between the two strains of rats involve a number of metabolic pathways and symbiotic gut microflora. SD rats exhibited higher individualized metabolic variations in the fasting and feeding states, and a stronger ability to recover from an altered metabolic profile with less hepatic injury from the consecutive ethanol exposure, as compared to Wistar rats. In summary, the GC/MS-based urinary metabolomics studies demonstrated an intrinsic metabolic difference between SD and Wistar rats, which warrants consideration in experimental design using these animal strains.
KW - Ethanol intervention
KW - GC/MS
KW - Metabolomics
KW - Sprague-Dawley rats
KW - Systematic difference
KW - Wistar rats
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U2 - 10.1007/s11306-010-0252-5
DO - 10.1007/s11306-010-0252-5
M3 - Article
AN - SCOPUS:80051664076
SN - 1573-3882
VL - 7
SP - 363
EP - 374
JO - Metabolomics
JF - Metabolomics
IS - 3
ER -