#METABOLOMICS WORKBENCH dmw178_20180911_072635 DATATRACK_ID:1499 STUDY_ID:ST001092 ANALYSIS_ID:AN001778 PROJECT_ID:PR000708
VERSION             	1
CREATED_ON             	November 6, 2018, 4:06 pm
#PROJECT
PR:PROJECT_TITLE                 	Metabolic approaches reveal the role of CAR in energy metabolism
PR:PROJECT_TYPE                  	Time Course
PR:PROJECT_SUMMARY               	The constitutive androstane receptor (CAR; NR1I3) contributes important
PR:PROJECT_SUMMARY               	regulatory roles in biotransformation, xenobiotic transport function, energy
PR:PROJECT_SUMMARY               	metabolism and lipid homeostasis. In this investigation, global serum and liver
PR:PROJECT_SUMMARY               	tissue metabolomes were assessed analytically in wild type and CAR-null
PR:PROJECT_SUMMARY               	transgenic mice using NMR, GC/MS and UPLC/MS-MS-based metabolomics.
PR:PROJECT_SUMMARY               	Significantly, CAR activation increased serum levels of fatty acids, lactate,
PR:PROJECT_SUMMARY               	ketone bodies and tricarboxylic acid cycle products, whereas levels of
PR:PROJECT_SUMMARY               	phosphatidylcholine, sphingomyelin, amino acids and liver glucose were decreased
PR:PROJECT_SUMMARY               	following short-term activation of CAR. Mechanistically, quantitative mRNA
PR:PROJECT_SUMMARY               	analysis demonstrated significantly decreased expression of key gluconeogenic
PR:PROJECT_SUMMARY               	pathways, and increased expression of glucose utilization pathways, changes
PR:PROJECT_SUMMARY               	likely resulting from down-regulation of the hepatic glucose sensor and
PR:PROJECT_SUMMARY               	bi-directional transporter, Glut2. Short-term CAR activation also resulted in
PR:PROJECT_SUMMARY               	enhanced fatty acid synthesis and impaired β-oxidation. In summary, CAR
PR:PROJECT_SUMMARY               	contributes an expansive role regulating energy metabolism, significantly
PR:PROJECT_SUMMARY               	impacting glucose, and monocarboxylic acid, as well as fatty acid metabolism and
PR:PROJECT_SUMMARY               	lipid homeostasis, through receptor-mediated regulation of several genes in
PR:PROJECT_SUMMARY               	multiple associated pathways.
PR:INSTITUTE                     	Pennsylvania State University
PR:LABORATORY                    	Omiecinski Lab
PR:LAST_NAME                     	Omiecinski
PR:FIRST_NAME                    	Curt
PR:ADDRESS                       	101 Life Sciences Building
PR:EMAIL                         	cjo10@psu.edu, dmw178@psu.edu
PR:PHONE                         	8148651572
#STUDY
ST:STUDY_TITLE                   	Metabolic profiling by NMR analysis in liver aqueous extract samples
ST:STUDY_TYPE                    	Time Course
ST:STUDY_SUMMARY                 	Liver tissue were harvested from wild type and CAR knockout mice treated for 48
ST:STUDY_SUMMARY                 	or 72h with or without TCPOBOP.
ST:INSTITUTE                     	Pennsylvania State University
ST:LABORATORY                    	Omiecinski Lab
ST:LAST_NAME                     	Omiecinski
ST:FIRST_NAME                    	Curt
ST:ADDRESS                       	101 Life Sciences Building
ST:EMAIL                         	cjo10@psu.edu, dmw178@psu.edu
ST:PHONE                         	8148651572
ST:NUM_GROUPS                    	8
ST:TOTAL_SUBJECTS                	48
ST:NUM_MALES                     	48
#SUBJECT
SU:SUBJECT_TYPE                  	Mammal
SU:SUBJECT_SPECIES               	Mus musculus
SU:TAXONOMY_ID                   	10090
SU:GENOTYPE_STRAIN               	Wild Type C57BL/6 and CAR Knockout
SU:AGE_OR_AGE_RANGE              	Approximately 8 weeks old
SU:GENDER                        	Male
SU:ANIMAL_LIGHT_CYCLE            	12 h
SU:ANIMAL_FEED                   	ad libitum
SU:ANIMAL_WATER                  	ad libitum
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_48H_101	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_48H_102	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_48H_103	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_48H_104	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_48H_105	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_48H_106	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_48H_201	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_48H_202	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_48H_203	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_48H_204	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_48H_205	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_48H_206	Genotype:WT | Time Point (h):48 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_72H_301	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_72H_302	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_72H_303	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_72H_304	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_72H_305	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_DMSO_72H_306	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):-	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_72H_401	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_72H_402	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_72H_403	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_72H_404	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_72H_405	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):2	
SUBJECT_SAMPLE_FACTORS           	-	WT_TCP_72H_406	Genotype:WT | Time Point (h):72 | TCPOBOP (mg/kg):2	
#COLLECTION
CO:COLLECTION_SUMMARY            	Liver tissue was snap-frozen in liquid nitrogen and stored at -80C.
CO:SAMPLE_TYPE                   	Liver
CO:STORAGE_CONDITIONS            	-80℃
#TREATMENT
TR:TREATMENT_SUMMARY             	Each mouse was treated with either a singel does of 2 mg/kg of Car agonist
TR:TREATMENT_SUMMARY             	(TCPOBOP) or the vehicle control via intraperitoneal injection.
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Liver tissue was homogenized in a methanol-water mixture, dried and resuspended
SP:SAMPLEPREP_SUMMARY            	in phosphate buffer containing TSP-d4.
SP:SAMPLEPREP_PROTOCOL_FILENAME  	NMR_metabolomics_protocol.pdf
SP:PROCESSING_METHOD             	Homogenization
SP:PROCESSING_STORAGE_CONDITIONS 	4℃
SP:EXTRACTION_METHOD             	Methanol/Water
SP:EXTRACT_STORAGE               	On ice
SP:SAMPLE_RESUSPENSION           	D2O
SP:SAMPLE_SPIKING                	TSP-d4
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_TYPE           	-
CH:INSTRUMENT_NAME               	-
CH:COLUMN_NAME                   	-
#ANALYSIS
AN:ANALYSIS_TYPE                 	NMR
AN:LABORATORY_NAME               	Omiecinski Lab
#NMR
NM:INSTRUMENT_NAME               	Bruker Avance III
NM:INSTRUMENT_TYPE               	FT-NMR
NM:NMR_EXPERIMENT_TYPE           	Other
NM:NMR_COMMENTS                  	NOESYPR1D
NM:SPECTROMETER_FREQUENCY        	600 MHz
NM:NMR_SOLVENT                   	D2O
NM:NMR_RESULTS_FILE              	ST001092_AN001778_Results.txt	UNITS:ppm
#END