نتایج جستجو برای: mcardle cells and vldl

تعداد نتایج: 17076115  

Journal: :Arteriosclerosis, Thrombosis, and Vascular Biology 1996

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2012
Lazar A Bojic Cynthia G Sawyez Dawn E Telford Jane Y Edwards Robert A Hegele Murray W Huff

OBJECTIVE Hypertriglyceridemia is an important risk factor for cardiovascular disease. Elevated plasma very low-density lipoprotein (VLDL) puts insulin-resistant patients at risk for atherosclerosis. VLDL readily induces macrophage lipid accumulation and inflammatory responses, for which targeted therapeutic strategies remain elusive. We examined the ability of VLDL to induce macrophage foam ce...

Journal: :Journal of lipid research 1993
A J Evans C G Sawyez B M Wolfe P W Connelly G F Maguire M W Huff

The present investigations have examined the mechanism(s) whereby Sf 60-400 very low density lipoproteins (VLDL) from Type IV hypertriglyceridemic subjects cause cholesteryl ester and triglyceride accumulation in J774 macrophages. Both apolipoprotein (apo) E-poor and apoE-rich Type IV VLDL subfractions, isolated by heparin-Sepharose chromatography, were capable of enhancing cellular cholesterol...

Journal: :Archives of neurology 2009
Susanne T Andersen Tina D Jeppesen Tanja Taivassalo Marie-Louise Sveen Katja Heinicke Ronald G Haller John Vissing

BACKGROUND The major fuel for exercising muscle at low exercise intensities is fat. OBJECTIVE To investigate the role of fat metabolism in McArdle disease (also known as glycogen storage disease type V), an inborn error of muscle glycogenolysis, by manipulating free fatty acid availability for oxidation during exercise. DESIGN Randomized, placebo-controlled, crossover trial. SETTING Hospi...

Journal: :Journal of lipid research 2011
Michelle Bamji-Mirza Meenakshi Sundaram Shumei Zhong Erik F Yao Robin J Parks Zemin Yao

Hepatic lipase (HL) plays a role in the catabolism of apolipoprotein (apo)B-containing lipoproteins through its lipolytic and ligand-binding properties. We describe a potential intracellular role of HL in the assembly and secretion of VLDL. Transient or stable expression of HL in McA-RH7777 cells resulted in decreased (by 40%) incorporation of [(3)H]glycerol into cell-associated and secreted tr...

Journal: :Physiological genomics 2016
Gisela Nogales-Gadea Richard Godfrey Alfredo Santalla Jaume Coll-Cantí Guillem Pintos-Morell Tomàs Pinós Joaquín Arenas Miguel Angel Martín Alejandro Lucia

McArdle disease (glycogen storage disease type V) is caused by inherited deficiency of a key enzyme in muscle metabolism, the skeletal muscle-specific isoform of glycogen phosphorylase, "myophosphorylase," which is encoded by the PYGM gene. Here we review the main pathophysiological, genotypic, and phenotypic features of McArdle disease and their interactions. To date, moderate-intensity exerci...

Journal: :Archives of neurology 2008
Susanne Tvede Andersen Ronald G Haller John Vissing

BACKGROUND Oral sucrose (75 g) ingested 40 minutes before exercise improves exercise tolerance in McArdle disease. OBJECTIVE To determine whether a lower dose of sucrose administered closer in time to exercise could have a similar beneficial effect on exercise capacity in patients with McArdle disease. DESIGN Placebo-controlled crossover. SETTING Neuromuscular Research Unit at the Departm...

Journal: :Neuromuscular Disorders 2017
Renata Siciliani Scalco Jasper M. Morrow Suzanne Booth Sherryl Chatfield Richard Godfrey Ros Quinlivan

Diagnosis of McArdle disease is frequently delayed by many years following the first presentation of symptoms to a health professional. The aim of this study was to investigate the importance of misdiagnosis in delaying diagnosis of McArdle disease. The frequency of misdiagnosis, duration of diagnostic delay, categories of misdiagnoses and inappropriate medical interventions were assessed in 50...

Journal: :Arteriosclerosis: An Official Journal of the American Heart Association, Inc. 1984

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