Search results for " Slow-Twitch"

showing 4 items of 14 documents

Absence of an aging-related increase in fiber type grouping in athletes and non-athletes

2020

The ageing-related loss of muscle mass is thought to be partly attributable to motor neuron loss and motor unit remodelling that result in fibre type grouping. We examined fibre type grouping in 19- to 85-year-old athletes and non-athletes and evaluated to which extent any observed grouping is explained by the fibre type composition of the muscle. Since regular physical activity may stimulate reinnervation, we hypothesised that fibre groups are larger in master athletes than in age-matched non-athletes. Fibre type grouping was assessed in m. vastus lateralis biopsies from 22 young (19-27 years) and 35 healthy older (66-82 years) non-athletes, and 14 young (20-29 years), 51 middle-aged (38%6…

MaleBiopsy030204 cardiovascular system & hematologyMuskel- und KnochenstoffwechselQuadriceps Muscleudc:612.74:612.660302 clinical medicinegroupingOrthopedics and Sports MedicineFibre typeAged 80 and overMotor NeuronsDenervationbiologyFiber typestaranjemišična vlaknaMiddle Agedfibre typeMuscle Fibers Slow-Twitchmedicine.anatomical_structureMuscle Fibers Fast-TwitchreinervacijaFemaleSportsReinnervationAdultmedicine.medical_specialtyPhysical Therapy Sports Therapy and RehabilitationYoung Adult03 medical and health sciencesInternal medicinevastus lateralismedicineHumansAgeddenervationbusiness.industryAthletesaging030229 sport sciencesMotor neuronbiology.organism_classificationfiber typereinnervationMotor unitdenervacijaCross-Sectional StudiesEndocrinologyAgeingbusiness
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Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred

2006

Abstract Myosin storage myopathy (OMIM 608358), a congenital myopathy characterised by subsarcolemmal, hyaline-like accumulations of myosin in Type I muscle fibres, was first described by Cancilla and Colleagues in 1971 [Neurology 1971;21:579–585] in two siblings as ‘familial myopathy with probable lysis of myofibrils in type I muscle fibres'. Two mutations in the slow skeletal myosin heavy chain gene ( MYH7 ) have recently been associated with the disease in other families. We have identified a novel heterozygous Leu1793Pro mutation in MYH7 in DNA from paraffin sections of one of the original siblings. This historical molecular analysis confirms the original cases had myosin storage myopat…

MaleHeterozygotemacromolecular substancesMyosinsBiologymedicine.disease_causeMuscular DiseasesMyofibrilsMyosinmedicineHumansMyopathyGeneGenetics (clinical)GeneticsMutationMyosin Heavy ChainsMyosin storage myopathyDNAExonsmedicine.diseaseMolecular biologyCongenital myopathyMuscle Fibers Slow-TwitchNeurologyChild PreschoolMutationPediatrics Perinatology and Child HealthFemaleMYH7Neurology (clinical)medicine.symptomMyofibrilCardiac MyosinsNeuromuscular Disorders
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Muscle fiber-type distribution predicts weight gain and unfavorable left ventricular geometry: a 19 year follow-up study

2006

Abstract Background Skeletal muscle consists of type-I (slow-twitch) and type-II (fast-twitch) fibers, with proportions highly variable between individuals and mostly determined by genetic factors. Cross-sectional studies have associated low percentage of type-I fibers (type-I%) with many cardiovascular risk factors. Methods We investigated whether baseline type-I% predicts left ventricular (LV) structure and function at 19-year follow-up, and if so, which are the strongest mediating factors. At baseline in 1984 muscle fiber-type distribution (by actomyosin ATPase staining) was studied in 63 healthy men (aged 32–58 years). The follow-up in 2003 included echocardiography, measurement of obes…

Malelcsh:Diseases of the circulatory (Cardiovascular) systemTime Factors030204 cardiovascular system & hematologyDoppler echocardiographyWeight GainBody fat percentageCohort StudiesVentricular Dysfunction Left0302 clinical medicineReference Valuesmedicine.diagnostic_testIncidenceBiopsy NeedleMiddle AgedEchocardiography Dopplermedicine.anatomical_structureMuscle Fibers Slow-TwitchCardiovascular DiseasesMuscle Fibers Fast-TwitchCardiologyRegression Analysismedicine.symptomCardiology and Cardiovascular MedicineResearch ArticleAdultmedicine.medical_specialtyWaistRisk AssessmentSensitivity and Specificity03 medical and health sciencesAge DistributionPredictive Value of TestsInternal medicineHeart ratemedicineHumansObesityMuscle SkeletalAngiologyAgedProbabilityRetrospective Studiesbusiness.industrySkeletal muscle030229 sport sciencesMyocardial ContractionBlood pressurelcsh:RC666-701businessWeight gainFollow-Up StudiesBMC Cardiovascular Disorders
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The metalloproteinase-disintegrin ADAM10 is exclusively expressed by type I muscle fibers.

2008

ADAM10 (Kuzbanian) is a member of a recently discovered family of membrane-anchored metalloproteinases with a complex and conserved domain structure. In part, these metalloproteinases have been implicated in muscle formation. Herein the expression pattern of ADAM10 in human skeletal muscle was studied. ADAM10 was found to be present in human myoblasts and to be exclusively expressed in type I fibers, suggesting that it may be critical in muscle fiber differentiation.

PhysiologyADAM10Matrix metalloproteinaseCellular and Molecular NeuroscienceADAM10 ProteinPhysiology (medical)DisintegrinmedicineMyocyteHumansAdenosine TriphosphatasesMetalloproteinasebiologyMyosin Heavy ChainsMyogenesisChemistrySkeletal muscleMembrane ProteinsCell biologyADAM Proteinsmedicine.anatomical_structureMuscle Fibers Slow-TwitchBiochemistrybiology.proteinNeurology (clinical)Amyloid Precursor Protein SecretasesITGA7Musclenerve
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