#METABOLOMICS WORKBENCH hormel101_20170623_145343 DATATRACK_ID:1099 STUDY_ID:ST000650 ANALYSIS_ID:AN000982 PROJECT_ID:PR000460
VERSION             	1
CREATED_ON             	June 26, 2017, 8:16 am
#PROJECT
PR:PROJECT_TITLE                 	The dystrophic muscle metabolome: effects of exercise and NO donor therapy
PR:PROJECT_SUMMARY               	"In Duchenne and Becker muscular dystrophy (DMD, BMD), loss of the cytoskeletal
PR:PROJECT_SUMMARY               	protein dystrophin weakens the sarcolemma and disrupts cellular signaling,
PR:PROJECT_SUMMARY               	rendering the diseased muscles susceptible to contractioninduced damage. We and
PR:PROJECT_SUMMARY               	others have shown that loss of neuronal nitric oxide synthase (nNOSμ) from the
PR:PROJECT_SUMMARY               	sarcolemma of dystrophin-deficient muscle causes functional muscle ischemia
PR:PROJECT_SUMMARY               	during exercise due to unopposed sympathetic vasoconstriction, thereby
PR:PROJECT_SUMMARY               	exacerbating fatigue and injury of the diseased muscles. Genetic and
PR:PROJECT_SUMMARY               	pharmacologic strategies targeting nNOSμ-NO signaling ameliorate functional
PR:PROJECT_SUMMARY               	muscle ischemia, as well as many other features of the dystrophic phenotype in
PR:PROJECT_SUMMARY               	the mdx mouse model of DMD/BMD. These findings suggest that the therapeutic
PR:PROJECT_SUMMARY               	benefit of NO likely extends beyond its vascular effects. A growing body of
PR:PROJECT_SUMMARY               	evidence indicates that NO directly influences muscle metabolism through effects
PR:PROJECT_SUMMARY               	on glucose transport as well as mitochondrial biogenesis and function. Both
PR:PROJECT_SUMMARY               	nNOS-/- mice and mdx mice exhibit muscle mitochondrial dysfunction, decreased
PR:PROJECT_SUMMARY               	resistance to fatigue, and exercise-induced muscle injury, suggesting a causal
PR:PROJECT_SUMMARY               	role of nNOSμ-NO deficiency. However, the specific metabolic changes resulting
PR:PROJECT_SUMMARY               	from reduced NO signaling that might render dystrophic muscle susceptible to
PR:PROJECT_SUMMARY               	fatigue and use-dependent injury remain poorly defined. Therefore, the goal of
PR:PROJECT_SUMMARY               	this pilot metabolomics study is to identify the unique biochemical profiles of
PR:PROJECT_SUMMARY               	skeletal and cardiac muscles of mdx mice to gain further mechanistic insight
PR:PROJECT_SUMMARY               	into the pathophysiological role of NO deficiency in muscular dystrophy. In Aim
PR:PROJECT_SUMMARY               	1, we will characterize the skeletal and cardiac muscle metabolomes of mdx and
PR:PROJECT_SUMMARY               	nNOS-/- mice at rest and following a single bout of treadmill exercise with the
PR:PROJECT_SUMMARY               	goal of discovering common metabolic signatures caused by loss of NO signaling.
PR:PROJECT_SUMMARY               	In Aim 2, we will evaluate the potential of a NO donor drug that is under
PR:PROJECT_SUMMARY               	development as a therapeutic for DMD/BMD to improve the skeletal and cardiac
PR:PROJECT_SUMMARY               	muscle metabolomes in mdx mice. As a result of this pilot study, we hope to gain
PR:PROJECT_SUMMARY               	new understanding of the metabolic derangements in dystrophin-deficient muscle,
PR:PROJECT_SUMMARY               	insight into the therapeutic effects of NO replacement, and to identify new
PR:PROJECT_SUMMARY               	pathogenic mechanisms and putative therapeutic targets that will form the basis
PR:PROJECT_SUMMARY               	of future grant applications."
PR:INSTITUTE                     	Mayo Clinic
PR:LAST_NAME                     	Thomas
PR:FIRST_NAME                    	Gail
PR:ADDRESS                       	Penn State Hershey Heart and Vascular Institute Penn State College of Medicine
PR:ADDRESS                       	500 University Drive, MC H047 Hershey, PA 17033
PR:EMAIL                         	gthomas4@hmc.psu.edu
PR:PHONE                         	717-531-0003, ext. 287087
#STUDY
ST:STUDY_TITLE                   	Effects of NO Donor Therapy on the Dystrophic Mouse Muscle TCA Cycle (part VI)
ST:STUDY_SUMMARY                 	For this aim, we will only use male mdx mice. We will study three groups treated
ST:STUDY_SUMMARY                 	for 7 days with vehicle, naproxcinod (i.e., NO-naproxen), or naproxen (n = 10
ST:STUDY_SUMMARY                 	each group). Two hours after the final treatment, half the mice in each group
ST:STUDY_SUMMARY                 	will be run to exhaustion on a treadmill. The heart and gastrocnemius, soleus,
ST:STUDY_SUMMARY                 	and quadriceps muscles of one hindlimb will be sent to the Mayo Clinic
ST:STUDY_SUMMARY                 	Metabolomics Resource Core. The heart and quadriceps muscle will be used for
ST:STUDY_SUMMARY                 	untargeted metabolomics profiling (LC/MS) while the gastrocnemius and soleus
ST:STUDY_SUMMARY                 	muscles will be used for targeted analyses of amino acids plus amino
ST:STUDY_SUMMARY                 	metabolites, non-esterified fatty acids, and citric acid cycle intermediates.
ST:INSTITUTE                     	Mayo Clinic
ST:LAST_NAME                     	Thomas
ST:FIRST_NAME                    	Gail
ST:ADDRESS                       	Penn State Hershey Heart and Vascular Institute Penn State College of Medicine
ST:ADDRESS                       	500 University Drive, MC H047 Hershey, PA 17033
ST:EMAIL                         	gthomas4@hmc.psu.edu
ST:PHONE                         	717-531-0003, ext. 287087
#SUBJECT
SU:SUBJECT_TYPE                  	Mouse
SU:SUBJECT_SPECIES               	Mus musculus
SU:TAXONOMY_ID                   	10090
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Additional sample data
SUBJECT_SAMPLE_FACTORS           	-	Sample # 1	Time point:Sedentary | Grouping:SED-Naproxcinod	Date of study=9/23/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 2	Time point:Sedentary | Grouping:SED-Naproxcinod	Date of study=9/24/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 3	Time point:Sedentary | Grouping:SED-Naproxcinod	Date of study=10/1/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 4	Time point:Sedentary | Grouping:SED-Naproxcinod	Date of study=10/7/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 5	Time point:Sedentary | Grouping:SED-Naproxcinod	Date of study=10/9/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 6	Time point:Post Run | Grouping:RUN-Naproxcinod	Date of study=9/23/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 7	Time point:Post Run | Grouping:RUN-Naproxcinod	Date of study=9/24/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 8	Time point:Post Run | Grouping:RUN-Naproxcinod	Date of study=10/1/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 9	Time point:Post Run | Grouping:RUN-Naproxcinod	Date of study=10/7/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 10	Time point:Post Run | Grouping:RUN-Naproxcinod	Date of study=10/9/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 11	Time point:Sedentary | Grouping:SED-Naproxen	Date of study=9/23/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 12	Time point:Sedentary | Grouping:SED-Naproxen	Date of study=9/24/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 13	Time point:Sedentary | Grouping:SED-Naproxen	Date of study=10/1/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 14	Time point:Sedentary | Grouping:SED-Naproxen	Date of study=10/7/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 15	Time point:Sedentary | Grouping:SED-Naproxen	Date of study=10/9/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 16	Time point:Post Run | Grouping:RUN-Naproxen	Date of study=9/23/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 17	Time point:Post Run | Grouping:RUN-Naproxen	Date of study=9/24/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 18	Time point:Post Run | Grouping:RUN-Naproxen	Date of study=10/1/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 19	Time point:Post Run | Grouping:RUN-Naproxen	Date of study=10/7/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 20	Time point:Post Run | Grouping:RUN-Naproxen	Date of study=10/9/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 21	Time point:Sedentary | Grouping:SED-Vehicle	Date of study=9/23/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 22	Time point:Sedentary | Grouping:SED-Vehicle	Date of study=9/24/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 23	Time point:Sedentary | Grouping:SED-Vehicle	Date of study=10/1/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 24	Time point:Sedentary | Grouping:SED-Vehicle	Date of study=10/7/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 25	Time point:Sedentary | Grouping:SED-Vehicle	Date of study=10/9/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 26	Time point:Post Run | Grouping:RUN-Vehicle	Date of study=9/23/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 27	Time point:Post Run | Grouping:RUN-Vehicle	Date of study=9/24/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 28	Time point:Post Run | Grouping:RUN-Vehicle	Date of study=10/1/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 29	Time point:Post Run | Grouping:RUN-Vehicle	Date of study=10/7/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
SUBJECT_SAMPLE_FACTORS           	-	Sample # 30	Time point:Post Run | Grouping:RUN-Vehicle	Date of study=10/9/2015; Gender=Male; Sample type=Tissue-Gastrocnemius; Species=Mouse
#COLLECTION
CO:COLLECTION_SUMMARY            	Blood and Tissue Harvesting: Mice will be euthanized and blood will be taken by
CO:COLLECTION_SUMMARY            	cardiac puncture, centrifuged, and the plasma will be stored at -80ºC. The
CO:COLLECTION_SUMMARY            	heart, diaphragm, and muscles of both hindlimbs (gastrocnemius, soleus,
CO:COLLECTION_SUMMARY            	quadriceps) will be dissected and snap frozen in liquid nitrogen. Tibialis
CO:COLLECTION_SUMMARY            	anterior and plantaris muscles from both hindlimbs also will be dissected and
CO:COLLECTION_SUMMARY            	one set will be snap frozen in liquid nitrogen while the other set will be
CO:COLLECTION_SUMMARY            	mounted in OCT and frozen in isopentane cooled by liquid nitrogen. Cryosections
CO:COLLECTION_SUMMARY            	will be used to evaluate disease activity and exercise-induced muscle injury by
CO:COLLECTION_SUMMARY            	staining with: (a) hematoxylin and eosin to assess gross morphology, cellular
CO:COLLECTION_SUMMARY            	infiltration, and necrosis, (b) anti-F4/80 to label macrophages, and (c)
CO:COLLECTION_SUMMARY            	anti-IgG or IgM to label damaged muscle fibers.
#TREATMENT
TR:TREATMENT_SUMMARY             	"Studies will be performed in 12-16 week old male mdx mice, C57BL10 control
TR:TREATMENT_SUMMARY             	mice, and nNOS-/- mice obtained from Jackson Laboratory. All protocols will be
TR:TREATMENT_SUMMARY             	approved by the Penn State College of Medicine Institutional Animal Care and Use
TR:TREATMENT_SUMMARY             	Committee. Drug Treatment: Mice will be treated with vehicle, naproxcinod (20
TR:TREATMENT_SUMMARY             	mg/kg/day) or equimolar naproxen (12.5mg/kg/day) once a day for 7 consecutive
TR:TREATMENT_SUMMARY             	days. To avoid the stress of oral gavage or ip injections in mdx mice, drug or
TR:TREATMENT_SUMMARY             	vehicle will be administered in a small volume of peanut butter. Most mice
TR:TREATMENT_SUMMARY             	readily consume the dosed peanut butter within 30 min. Terminal experiments will
TR:TREATMENT_SUMMARY             	be performed 2 hours after the final dose is consumed."
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	mouse gastrocnemius TCA cyle
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_TYPE           	GC
CH:INSTRUMENT_NAME               	Agilent 7890B
CH:COLUMN_NAME                   	Agilent HP5-MS (30m × 0.25mm, 0.25 um)
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:MS_COMMENTS                   	-
MS:INSTRUMENT_NAME               	Agilent 5977A
MS:INSTRUMENT_TYPE               	Single quadrupole
MS:MS_TYPE                       	EI
MS:ION_MODE                      	POSITIVE
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS         	picomoles/mg
MS_METABOLITE_DATA_START
Samples	Sample # 1	Sample # 2	Sample # 3	Sample # 4	Sample # 5	Sample # 6	Sample # 7	Sample # 8	Sample # 9	Sample # 10	Sample # 11	Sample # 12	Sample # 13	Sample # 14	Sample # 15	Sample # 16	Sample # 17	Sample # 18	Sample # 19	Sample # 20	Sample # 21	Sample # 22	Sample # 23	Sample # 24	Sample # 25	Sample # 26	Sample # 27	Sample # 28	Sample # 29	Sample # 30
Factors	Time point:Sedentary | Grouping:SED-Naproxcinod	Time point:Sedentary | Grouping:SED-Naproxcinod	Time point:Sedentary | Grouping:SED-Naproxcinod	Time point:Sedentary | Grouping:SED-Naproxcinod	Time point:Sedentary | Grouping:SED-Naproxcinod	Time point:Post Run | Grouping:RUN-Naproxcinod	Time point:Post Run | Grouping:RUN-Naproxcinod	Time point:Post Run | Grouping:RUN-Naproxcinod	Time point:Post Run | Grouping:RUN-Naproxcinod	Time point:Post Run | Grouping:RUN-Naproxcinod	Time point:Sedentary | Grouping:SED-Naproxen	Time point:Sedentary | Grouping:SED-Naproxen	Time point:Sedentary | Grouping:SED-Naproxen	Time point:Sedentary | Grouping:SED-Naproxen	Time point:Sedentary | Grouping:SED-Naproxen	Time point:Post Run | Grouping:RUN-Naproxen	Time point:Post Run | Grouping:RUN-Naproxen	Time point:Post Run | Grouping:RUN-Naproxen	Time point:Post Run | Grouping:RUN-Naproxen	Time point:Post Run | Grouping:RUN-Naproxen	Time point:Sedentary | Grouping:SED-Vehicle	Time point:Sedentary | Grouping:SED-Vehicle	Time point:Sedentary | Grouping:SED-Vehicle	Time point:Sedentary | Grouping:SED-Vehicle	Time point:Sedentary | Grouping:SED-Vehicle	Time point:Post Run | Grouping:RUN-Vehicle	Time point:Post Run | Grouping:RUN-Vehicle	Time point:Post Run | Grouping:RUN-Vehicle	Time point:Post Run | Grouping:RUN-Vehicle	Time point:Post Run | Grouping:RUN-Vehicle
Lactate	14596.64511	16420.75983	15126.27525	16619.35266	19997.61534	19556.71475	22035.84166	15516.69709	18657.12426	13890.31759	18515.1742	20781.34894	21125.14994	14804.14821	26545.65113	8987.286032	20955.02826	14359.45038	19600.56498	18546.67448	19987.22389	14795.49088	14004.70925	23941.41968	13768.44387	19809.28376	15756.93677	14659.87655	18097.78279	16134.22994
Succinate	44.01633422	44.63672492	24.4127468	34.4418587	39.18839369	45.84325129	52.52413725	50.95848631	58.41268935	27.29246514	27.42818412	29.39479483	29.83524329	16.81996589	56.58251072	16.02763062	50.5412443	22.79770221	33.68454134	30.17677559	35.47640262	19.35292991	37.61946861	57.17342453	20.06497305	29.9802799	16.7974661	32.30513499	35.64087901	62.26259665
Fumarate	127.2430232	154.1698097	152.1796124	114.4404551	144.8785357	203.3937752	239.7540176	211.8967311	173.2402948	103.9920769	172.6543471	140.846423	154.4585281	131.1940718	144.0891663	154.3924845	192.3715068	148.6130466	210.0063672	207.2661194	155.4493438	157.9170417	108.0915115	197.3208578	147.5172929	195.1305304	166.2379325	142.1466807	209.891747	150.4474527
Oxaloacetate	0.302156462	0.331549227	0.213636957	0.232613134	0.216575598	0.284003421	0.286940844	0.331851737	0.324075865	0.327793732	0.276883479	0.36578117	0.328351776	0.339625445	0.269680298	0.226843447	0.272980568	0.250027015	0.192654768	0.248192886	0.299789789	0.354374226	0.327781903	0.327422014	0.332158878	0.310166521	0.284072916	0.412354038	0.475129383	0.445001851
Ketoglutarate	4.058147269	0.888284681	0.337554008	0.244860583	0.183112618	0.125413665	0.150015532	0.20247586	0.165656685	0.182440629	0.118767281	0.114767885	0.140505008	0.143395016	0.118948331	0.097545059	0.187915903	0.108669324	0.097815555	0.168506967	0.168039891	0.125142349	0.072906121	0.359036879	0.101943355	0.154594965	0.158347176	0.099390884	0.189123609	0.132391065
Malate	114.6728535	139.3540793	134.6312574	102.1387162	127.2927452	178.5011073	210.1390342	186.4425887	152.465831	96.45748433	153.9469339	125.3246053	137.2693175	115.045303	125.7996698	140.0564758	170.4749068	133.6776947	185.9337925	185.6666698	137.7935408	140.4353031	95.55244955	175.036296	132.3052911	173.9270855	136.757557	125.7796362	186.6916021	132.601348
2-Hydroxyglutarate	5.772210803	4.896599217	6.833668806	8.611665194	5.67520246	7.037465781	6.140841289	5.548828021	5.187760446	4.018313441	4.471823337	3.777857881	3.92415097	4.287781888	4.738517965	3.849364655	5.694905974	4.406578802	5.534862731	8.495301408	5.794653003	4.974903909	3.53283756	7.943746858	4.909560917	5.871592884	5.333829761	5.376779685	6.479829786	8.82091876
cis-Aconitic Acid	1.863194344	1.332655822	1.534438887	1.739507279	1.722795158	1.315756369	1.971697938	1.549910097	1.911311903	1.169436045	1.395744277	1.360608215	1.180386354	1.243824431	1.141821224	1.058867509	2.266932166	1.500296393	1.27310081	1.75128231	1.665329161	1.803913611	0.666260104	2.55731557	1.077358542	2.31685421	1.278538044	0.775829275	2.610668773	1.621287821
Citrate	65.13873867	54.8124167	79.5190848	85.11545593	87.63940273	77.62639995	103.4953624	70.80183789	119.3361431	72.68088998	77.95616282	68.75581453	67.49675906	72.89367102	51.05610849	58.4899187	115.4305464	88.50698182	75.90352169	98.283215	90.4882571	84.38743472	37.78458597	132.1414579	62.94466182	100.4218888	82.736994	64.96383015	120.4373076	81.62003565
Isocitrate	10.83051153	9.174140486	10.9528954	11.36902688	12.38726008	8.682194076	10.36972558	7.751696903	12.39787639	8.501532609	10.44417435	9.493869484	6.93364463	7.660011787	7.182636151	4.052252012	12.72283046	6.582370659	8.044852403	6.385482631	10.33120857	8.87693766	4.814773003	11.3367726	7.708240047	8.402129937	8.377875439	5.635094858	10.28049366	5.670032493
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name
Lactate
Succinate
Fumarate
Oxaloacetate
Ketoglutarate
Malate
2-Hydroxyglutarate
cis-Aconitic Acid
Citrate
Isocitrate
METABOLITES_END
#END