Search results for "Dystrophy"

showing 10 items of 268 documents

Alterations of intestinal transit and fecal output in dystrophic mdx mice.

2009

Duchenne Muscular Dystrophy smooth muscle.Settore BIO/09 - Fisiologia
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Proteomic analysis of skeletal muscle in dystrophic (mdx) mice subject to low-intensity endurance exercise

2014

La rigenerazione del muscolo scheletrico in risposta ad un trauma dipende, dal tipo di lesione come contusione, deformazione e lacerazione e della gravità. Molti fattori regolatori svolgono un ruolo importante nella rigenerazione muscolare e uno di loro è l'esercizio fisico. Come l’esercizio fisico influisca sui muscoli dipende sia dalla modalità,dall’ intensità e durata dell’ allenamento e dslle caratteristiche specifiche del muscolo scheletrico in questione. Il primo obiettivo di questo studio è stato esaminare come l’esercizio di resistenza a bassa intensità influisca sul processo di rigenerazione in ratti con danno muscolare di tipo meccanico. I ratti sono stati divisi in tre gruppi: se…

Duchenne Muscular DystrophySettore BIO/09 - Fisiologia
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Increased bronchial epithelial thickness in small airways of mdx mice at rest and after exercise training

2009

Duchenne muscolar dystrophy low intensity endurance training bronchiolar epitheliumSettore MED/10 - Malattie Dell'Apparato RespiratorioSettore BIO/09 - Fisiologia
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Bronchial epithelial thickness is increased in small airways of MDX mise at rest and after training

2009

Duchenne muscolar dystrophy low-intensity endurance training bronchiolar epithelium thicknessSettore MED/10 - Malattie Dell'Apparato RespiratorioSettore BIO/09 - Fisiologia
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Memory deficit of children with Duchenne muscular dystrophy

2007

Several studies on intelligence of children suffering from Duchenne muscular dystrophy (DMD) found impairments in linguistic functions and memory. Memory deficit mainly involves long-term memory; short-term memory impairment was also present, even if less frequently. Some studies tried to establish a correlation between the distal deletion of the dystrophin gene and low intelligence levels. The present study investigated the neuropsychological performance in a group of DMD children (26 subjects); neuropsychological tests included: Wechsler intelligence scale for children-revised; Raven’s progressive matrices test; Rey’s complex figure test; memory and digit span tests; Benton’s visual reten…

Duchenne muscular dystrophy childrenSettore MED/39 - Neuropsichiatria Infantile
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Early alterations of the behavioural structure of mice affected by Duchenne muscular dystrophy and tested in open-field

2020

Present study has been carried out to assess whether early alterations of the behavioural structure may be detected in mice affected by Duchenne muscular dystrophy (DMD). To this purpose, both quantitative and T-pattern analysis (TPA) were used to analyse the behaviour of two groups of male, two months old mice, 18 MDX and 18 normal as control, tested in an open-field apparatus. T-pattern analysis is a multivariate technique able to reveal hidden structural features of behaviour and, in particular, its temporal characteristics. As to quantitative analyses, mean durations evidenced a significant increase of Walking, Modified Climbing and Rearing and a significant reduction of Immobile-Sniffi…

Duchenne muscular dystrophyMalemdx mouseDuchenne muscular dystrophyCombined usePhysiologyBiologySettore BIO/09 - FisiologiaOpen fieldMice03 medical and health sciencesBehavioral Neuroscience0302 clinical medicineSniffingDMDImage Processing Computer-AssistedmedicineAnimalsMuscle Skeletal030304 developmental biologyBehavioural repertoire0303 health sciencesBehavior AnimalT-pattern analysimedicine.diseaseMice Inbred C57BLMuscular Dystrophy DuchenneMDX mouseDisease Models AnimalClimbingMultivariate AnalysisMice Inbred mdxTPALicking030217 neurology & neurosurgeryBehavioural Brain Research
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MMP-10 Is Required for Efficient Muscle Regeneration in Mouse Models of Injury and Muscular Dystrophy

2013

Abstract Matrix metalloproteinases (MMPs), a family of endopeptidases that are involved in the degradation of extracellular matrix components, have been implicated in skeletal muscle regeneration. Among the MMPs, MMP-2 and MMP-9 are upregulated in Duchenne muscular dystrophy (DMD), a fatal X-linked muscle disorder. However, inhibition or overexpression of specific MMPs in a mouse model of DMD (mdx) has yielded mixed results regarding disease progression, depending on the MMP studied. Here, we have examined the role of MMP-10 in muscle regeneration during injury and muscular dystrophy. We found that skeletal muscle increases MMP-10 protein expression in response to damage (notexin) or diseas…

Duchenne muscular dystrophyMatrix metalloproteinaseBiologyMuscle disorderMuscular DystrophiesExtracellular matrixMiceMatrix Metalloproteinase 10medicineAnimalsHumansRegenerationMuscular dystrophyMuscle SkeletalRegeneration (biology)Skeletal muscleCell BiologyAnatomymedicine.diseaseCell biologyDisease Models Animalmedicine.anatomical_structureMatrix Metalloproteinase 9Mice Inbred mdxMatrix Metalloproteinase 2Molecular MedicineITGA7Developmental BiologyStem Cells
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Long-Term Ventilation in Neuromuscular Patients: Review of Concerns, Beliefs, and Ethical Dilemmas

2019

<b><i>Background:</i></b> Noninvasive mechanical ventilation (NIV) is an effective treatment in patients with neuromuscular diseases (NMD) to improve symptoms, quality of life, and survival. <b><i>Summary:</i></b> NIV should be used early in the course of respiratory muscle involvement in NMD patients and its requirements may increase over time. Therefore, training on technical equipment at home and advice on problem solving are warranted. Remote monitoring of ventilator parameters using built-in ventilator software is recommended. Telemedicine may be helpful in reducing hospital admissions. Anticipatory planning and palliative care should be …

Duchenne muscular dystrophyPulmonary and Respiratory MedicineRespiratory Therapymedicine.medical_specialtyTelemedicineTime FactorsPalliative caremedicine.medical_treatmentNeuromuscular disorderHome care03 medical and health sciencesTracheostomy0302 clinical medicineQuality of life (healthcare)Health caremedicineRespiratory muscleHumansIn patient030212 general & internal medicineIntensive care medicineAmyotrophic lateral sclerosiAmyotrophic lateral sclerosis; Duchenne muscular dystrophy; Home care; Neuromuscular disorders; Noninvasive ventilation; TracheostomyMechanical ventilationbusiness.industryNeuromuscular DiseasesAmyotrophic lateral sclerosisRespiration Artificial030228 respiratory systemQuality of LifeRespiratory InsufficiencybusinessNoninvasive ventilationNeuromuscular disordersFollow-Up StudiesLong term ventilationRespiration
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Myogenic NOS and endogenous NO production are defective in colon from dystrophic (mdx) mice

2001

The aim of the present study was to evaluate whether alterations in the distribution and/or function of nitric oxide synthase (NOS) could be involved in the development of the spontaneous mechanical tone observed in colon from dystrophic (mdx) mice. By recording the intraluminal pressure of isolated colon from normal mice, we showed that Nω-nitro-L-arginine methyl ester (L-NAME) increased the tone, even in the presence of tetrodotoxin. The effect was prevented by L-arginine, nifedipine, or Ca2+-free solution. In colon from mdx mice, L-NAME was ineffective. Immunohistochemistry revealed that the presence and distribution of neuronal (nNOS), endothelial, and inducible NOS isoforms in smooth m…

Duchenne muscular dystrophySpontaneous tonePhysiologyNitric oxide synthasePhysiology (medical)GastroenterologyNitric oxideImmunohistochemistrySettore BIO/09 - FisiologiaIntestinal smooth muscle
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An attempt to enhance neurogenesis of mdx mice via aerobic exercise and myostatin inhibition

2013

Duchennen lihasdystrofia (DMD) on perinnöllinen sairaus, jonka esiintyvyys on noin 1/3600 poikavauvasta. Siihen liittyy lihasten heikkoutta, rappeutumista ja kognitiivista vajavaisuutta. Taudin aiheuttaa mutatoitunut geeni dystrophiini proteiinille. On esitetty, että kognitiivinen vajavaisuus johtuu taudin vaikutuksesta ehkäistä neurogeneesiä. Neurogeneesi on prosessi, joka jatkuvasti synnyttää uusia hermosoluja pääasiallisesti subventikulaari alueella ja hippokampuksen dentate gyruksella. Hoitoa ja parannusta tautiin tutkitaan yleensä mdx-hiirillä, joiden taudin etiologia on riittävän lähellä ihmisten tautia. Tämä tutkimus keskittyy pyrkimykseen vaikuttaa mdx-hiirten neurogeneesiin aerobis…

Duchenne muscular dystrophyaerobic exerciseneurogeneesimyostatin blockermyostatiininitric oxideNeurogenesismdx miceDuchennen lihasdystrofiaaerobinen harjoittelu
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