Literature DB >> 22821188

Nitric oxide in myogenesis and therapeutic muscle repair.

Clara De Palma1, Emilio Clementi.   

Abstract

Nitric oxide is a short-lived intracellular and intercellular messenger. The first realisation that nitric oxide is important in physiology occurred in 1987 when its identity with the endothelium-derived relaxing factor was discovered. Subsequent studies have shown that nitric oxide possesses a number of physiological functions that are essential not only to vascular homeostasis but also to neurotransmission, such as in the processes of learning and memory and endocrine gland regulation, as well as inflammation and immune responses. The discovery in 1995 that a splice variant of the neuronal nitric oxide synthase is localised at the sarcolemma via the dystrophin-glycoprotein complex and of its displacement in Duchenne muscular dystrophy has stimulated a host of studies exploring the role of nitric oxide in skeletal muscle physiology. Recently, nitric oxide has emerged as a relevant messenger also of myogenesis that it regulates at several key steps, especially when the process is stimulated for muscle repair following acute and chronic muscle injuries. Here, we will review briefly the mechanisms and functions of nitric oxide in skeletal muscle and discuss its role in myogenesis, with specific attention to the promising nitric oxide-based approaches now being explored at the pre-clinical and clinical level for the therapy of muscular dystrophy.

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Year:  2012        PMID: 22821188     DOI: 10.1007/s12035-012-8311-8

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN: 0893-7648            Impact factor:   5.590


  125 in total

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8.  Nitric oxide represses inhibitory kappaB kinase through S-nitrosylation.

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Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-07       Impact factor: 11.205

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Review 10.  Nitric oxide, a biological double-faced janus--is this good or bad?

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2.  Skeletal muscle as an endogenous nitrate reservoir.

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4.  Integrating molecular mechanisms with synaptic plasticity in neurological disease.

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6.  Long-term treatment with naproxcinod significantly improves skeletal and cardiac disease phenotype in the mdx mouse model of dystrophy.

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Journal:  Hum Mol Genet       Date:  2014-01-23       Impact factor: 6.150

7.  Requirement of inducible nitric oxide synthase for skeletal muscle regeneration after acute damage.

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Review 10.  Turn up the power - pharmacological activation of mitochondrial biogenesis in mouse models.

Authors:  J C Komen; D R Thorburn
Journal:  Br J Pharmacol       Date:  2014-04       Impact factor: 8.739

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