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Oxidative stress, mitochondrial dysfunction and, inflammation common events in skin of patients with Fibromyalgia
dc.contributor.author | Sánchez-Domínguez B. | |
dc.contributor.author | Bullón P. | |
dc.contributor.author | Román-Malo L. | |
dc.contributor.author | Marín-Aguilar F. | |
dc.contributor.author | Alcocer-Gómez E. | |
dc.contributor.author | Carrión A.M. | |
dc.contributor.author | Sánchez-Alcazar J.A. | |
dc.contributor.author | Cordero M.D. | |
dc.date.accessioned | 2020-09-02T22:28:50Z | |
dc.date.available | 2020-09-02T22:28:50Z | |
dc.date.issued | 2015 | |
dc.identifier | 10.1016/j.mito.2015.01.010 | |
dc.identifier.citation | 21, , 69-75 | |
dc.identifier.issn | 15677249 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12728/6364 | |
dc.description | Fibromyalgia is a chronic pain syndrome with unknown etiology. Recent studies have shown some evidence demonstrating that oxidative stress, mitochondrial dysfunction and inflammation may have a role in the pathophysiology of fibromyalgia. Despite several skin-related symptoms accompanied by small fiber neuropathy have been studied in FM, these mitochondrial changes have not been yet studied in this tissue. Skin biopsies from patients showed a significant mitochondrial dysfunction with reduced mitochondrial chain activities and bioenergetics levels and increased levels of oxidative stress. These data were related to increased levels of inflammation and correlated with pain, the principal symptom of FM. All these parameters have shown a role in peripheral nerve damage which has been observed in FM as a possible responsible to allodynia. Our findings may support the role of oxidative stress, mitochondrial dysfunction and inflammation as interdependent events in the pathophysiology of FM with a special role in the peripheral alterations. © 2015 Elsevier B.V. | |
dc.language.iso | en | |
dc.publisher | Elsevier | |
dc.subject | Fibromyalgia | |
dc.subject | Inflammation | |
dc.subject | Mitochondrial dysfunction | |
dc.subject | Oxidative stress | |
dc.subject | adenosine triphosphate | |
dc.subject | cytochrome c oxidase | |
dc.subject | mitochondrial DNA | |
dc.subject | mitochondrial protein | |
dc.subject | reduced nicotinamide adenine dinucleotide dehydrogenase (ubiquinone) | |
dc.subject | succinate dehydrogenase (ubiquinone) | |
dc.subject | tumor necrosis factor alpha | |
dc.subject | ubidecarenone | |
dc.subject | ubiquinol cytochrome c reductase | |
dc.subject | adult | |
dc.subject | Article | |
dc.subject | bioenergy | |
dc.subject | clinical article | |
dc.subject | controlled study | |
dc.subject | disorders of mitochondrial functions | |
dc.subject | enzyme activity | |
dc.subject | female | |
dc.subject | fibromyalgia | |
dc.subject | human | |
dc.subject | human tissue | |
dc.subject | inflammation | |
dc.subject | middle aged | |
dc.subject | oxidative stress | |
dc.subject | pathogenesis | |
dc.subject | peripheral nerve injury | |
dc.subject | protein expression | |
dc.subject | skin biopsy | |
dc.subject | biopsy | |
dc.subject | energy metabolism | |
dc.subject | fibromyalgia | |
dc.subject | inflammation | |
dc.subject | mitochondrion | |
dc.subject | pain | |
dc.subject | pathology | |
dc.subject | pathophysiology | |
dc.subject | peripheral nerve | |
dc.subject | physiology | |
dc.subject | skin | |
dc.subject | Adult | |
dc.subject | Biopsy | |
dc.subject | Energy Metabolism | |
dc.subject | Female | |
dc.subject | Fibromyalgia | |
dc.subject | Humans | |
dc.subject | Inflammation | |
dc.subject | Middle Aged | |
dc.subject | Mitochondria | |
dc.subject | Oxidative Stress | |
dc.subject | Pain | |
dc.subject | Peripheral Nerves | |
dc.subject | Skin | |
dc.title | Oxidative stress, mitochondrial dysfunction and, inflammation common events in skin of patients with Fibromyalgia | |
dc.type | Article |