#METABOLOMICS WORKBENCH STUDY_ID:ST000185 ANALYSIS_ID:AN000285 PROJECT_ID:PR000158
VERSION             	1
CREATED_ON          	01-15-2019
#PROJECT
PR:PROJECT_TITLE                 	LEC metabolomics
PR:PROJECT_SUMMARY               	Comparison of metabolomic profile in LECs derived from normal and shunt animals
PR:INSTITUTE                     	University of California, San Francisco
PR:DEPARTMENT                    	Pediatrics
PR:LABORATORY                    	Fineman Lab
PR:LAST_NAME                     	Fineman
PR:FIRST_NAME                    	Jeffrey
PR:ADDRESS                       	San Francisco, CA
PR:EMAIL                         	jeff.fineman@ucsf.edu
PR:PHONE                         	415-502-6390
PR:DOI                           	http://dx.doi.org/10.21228/M8T01Q
#STUDY
ST:STUDY_TITLE                   	Fetal Lambs vascular graft Normal v Shunt LECs
ST:STUDY_TYPE                    	Glycolysis/TCA/Nucleotide analysis (tissue/cells)
ST:STUDY_SUMMARY                 	We recently reported superior right ventricle (RV) performance in response to
ST:STUDY_SUMMARY                 	acute afterload challenge in lambs with a model of congenital heart disease with
ST:STUDY_SUMMARY                 	chronic left-to-right cardiac shunts. Compared with control animals, shunt lambs
ST:STUDY_SUMMARY                 	demonstrated increased contractility because of an enhanced Anrep effect (the
ST:STUDY_SUMMARY                 	slow increase in contractility following myocyte stretch). This advantageous
ST:STUDY_SUMMARY                 	physiological response may reflect preservation of a fetal phenotype, since the
ST:STUDY_SUMMARY                 	RV of shunt lambs remains exposed to increased pressure postnatally. Nitric
ST:STUDY_SUMMARY                 	oxide (NO) production by NO synthase (NOS) is activated by myocyte stretch and
ST:STUDY_SUMMARY                 	is a necessary intermediary of the Anrep response. The purpose of this study was
ST:STUDY_SUMMARY                 	to test the hypothesis that NO signaling is increased in the RV of fetal lambs
ST:STUDY_SUMMARY                 	compared with controls and shunt lambs have persistence of this fetal pattern.
ST:STUDY_SUMMARY                 	An 8-mm graft was placed between the pulmonary artery and aorta in fetal lambs
ST:STUDY_SUMMARY                 	(shunt). NOS isoform expression, activity, and association with activating
ST:STUDY_SUMMARY                 	cofactors were determined in fetal tissue obtained during late-gestation and in
ST:STUDY_SUMMARY                 	4-wk-old juvenile shunt and control lambs. We demonstrated increased RNA and
ST:STUDY_SUMMARY                 	protein expression of NOS isoforms and increased total NOS activity in the RV of
ST:STUDY_SUMMARY                 	both shunt and fetal lambs compared with control. We also found increased NOS
ST:STUDY_SUMMARY                 	activation and association with cofactors in shunt and fetal RV compared with
ST:STUDY_SUMMARY                 	control. These data demonstrate preserved fetal NOS phenotype and NO signaling
ST:STUDY_SUMMARY                 	in shunt RV, which may partially explain the mechanism underlying the adaptive
ST:STUDY_SUMMARY                 	response to increased afterload seen in the RV of shunt lambs. Research is
ST:STUDY_SUMMARY                 	published, core data not used but project description is relevant:
ST:STUDY_SUMMARY                 	http://ajpheart.physiology.org/content/309/1/H157.long
ST:INSTITUTE                     	University of Michigan
ST:DEPARTMENT                    	Biomedical Research Core Facilities
ST:LABORATORY                    	Metabolomics core
ST:LAST_NAME                     	Kachman
ST:FIRST_NAME                    	Maureen
ST:ADDRESS                       	6300 Brehm Tower, 1000 Wall Street, Ann Arbor, MI 48105-5714
ST:EMAIL                         	mkachman@umich.edu
ST:PHONE                         	-
#SUBJECT
SU:SUBJECT_TYPE                  	Animal
SU:SUBJECT_SPECIES               	Ovis aries
SU:TAXONOMY_ID                   	9940
SU:SPECIES_GROUP                 	Mammal
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	SU0011546	S00017020	Type:increased flow	
SUBJECT_SAMPLE_FACTORS           	SU0011547	S00017021	Type:increased flow	
SUBJECT_SAMPLE_FACTORS           	SU0011548	S00017022	Type:increased flow	
SUBJECT_SAMPLE_FACTORS           	SU0011543	S00017017	Type:normal control	
SUBJECT_SAMPLE_FACTORS           	SU0011544	S00017018	Type:normal control	
SUBJECT_SAMPLE_FACTORS           	SU0011545	S00017019	Type:normal control	
#COLLECTION
CO:SAMPLE_TYPE                   	Endothelial Cells
CO:COLLECTION_SUMMARY            	-
#TREATMENT
TR:TREATMENT_SUMMARY             	-
#SAMPLEPREP
SP:SAMPLEPREP_PROTOCOL_FILENAME  	Gly-TCA-nucleotides_analysis_protocol-2015-03-09.docx
SP:SAMPLEPREP_SUMMARY            	-
#CHROMATOGRAPHY
CH:METHODS_ID                    	AQM011
CH:METHODS_FILENAME              	ALPHA_KETO_ACIDS-FULL.M.zip
CH:INSTRUMENT_NAME               	Agilent 7890A
CH:COLUMN_NAME                   	Agilent DB5-MS (30m × 0.25mm, 0.25um)
CH:CHROMATOGRAPHY_TYPE           	GC
#ANALYSIS
AN:LABORATORY_NAME               	MRC2 (University of Michigan)
AN:ANALYSIS_TYPE                 	MS
AN:ACQUISITION_PARAMETERS_FILE   	ALPHA_KETO_ACIDS-FULL.M.zip
#MS
MS:MS_COMMENTS                   	-
MS:INSTRUMENT_NAME               	Agilent 5975C
MS:INSTRUMENT_TYPE               	Single quadrupole
MS:MS_TYPE                       	EI
MS:ION_MODE                      	POSITIVE
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS         	pmol/µg protein
MS_METABOLITE_DATA_START
Samples	S00017020	S00017021	S00017022	S00017017	S00017018	S00017019
Factors	Type:increased flow	Type:increased flow	Type:increased flow	Type:normal control	Type:normal control	Type:normal control	
alpha-Ketoglutarate	23.9633	97.6063	25.9218	10.2784	18.6104	4.0044
Aspartate	28.9800	53.3015	30.6237	46.9567	68.9472	14.6040
fumarate	7.9338	15.4468	6.3243	9.4925	16.9246	3.5431
Glutamate	790.1819	2101.6621	615.9909	600.9693	920.9131	182.8471
Lactate	16463.0497	90098.3522	25552.9804	2325.6219	5968.9836	684.1921
pyruvate	48.1264	173.4467	68.0630	44.0311	115.6702	13.8828
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	pubchem_id	inchi_key	kegg_id	other_id	other_id_type	ri	ri_type	moverz_quant	
alpha-Ketoglutarate	51		C00026	AKG	UM_Target_ID				
Aspartate	5960		C00049	ASP	UM_Target_ID				
fumarate	444972		C00122	FUM	UM_Target_ID				
Glutamate	611			GLU	UM_Target_ID				
Lactate	107689		C00186	LAC	UM_Target_ID				
pyruvate	1060		C00022	PYR	UM_Target_ID				
METABOLITES_END
#END