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2016 | 16 | 3 | 136–145
Article title

Stres oksydacyjny w patogenezie stwardnienia rozsianego. Nowe możliwości terapeutyczne

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EN
Oxidative stress in the pathogenesis of multiple sclerosis. New possibilities of treatment
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Abstracts
EN
Multiple sclerosis is a progressive inflammatory and demyelinating disease of the central nervous system. Although the primary cause of this disease has not been established yet, it is known that destruction of myelin sheaths and loss of neurons and oligodendrocytes can be observed as disease progresses. It has been suggested that a  possible link between neuroinflammation and neurodegeneration could be the phenomenon of oxidative stress. Oxidative stress develops when there are too many free radicals produced within the cell, and the natural antioxidative mechanisms are not effective enough to dispose of them. It has been proven to contribute to the pathomechanism of such neurodegenerative disorders as Parkinson’s disease or Alzheimer’s disease. The role of oxidative stress in the pathogenesis of multiple sclerosis has also been recently confirmed, establishing it as a new target in the disease’s management. Even though the efficacy of such antioxidants as polyphenols, vitamins (A, C, E) and alpha-lipoic acid has been confirmed in many preclinical experiments, no significant effect has been shown in clinical trials. However, some clinical trials related to the use of antioxidants in multiple sclerosis treatment are still in progress. One compound with antioxidant potential that has been proven effective and safe in both preclinical and clinical trials is dimethyl fumarate. It was licensed for the treatment of multiple sclerosis in 2013. Even though its mechanism of action has not been fully established, one of its known effects is the induction of antioxidant pathway related to Nrf2 transcription factor and synthesis of antioxidant enzymes, leading to decrease in oxidative stress.
PL
Stwardnienie rozsiane to choroba zapalno-demielinizacyjna ośrodkowego układu nerwowego o dotychczas nieznanej przyczynie. W przebiegu stwardnienia rozsianego następuje uszkodzenie osłonki mielinowej komórek nerwowych oraz śmierć neuronów i  oligodendrocytów. W  ostatnich latach zwrócono uwagę, że ogniwem łączącym proces zapalny z neurodegeneracją może być stres oksydacyjny, czyli przewaga tworzenia wolnych rodników nad ich eliminacją przez systemy antyoksydacyjne komórki. Udowodniono, iż stres oksydacyjny ma związek z  patogenezą wielu chorób neurodegeneracyjnych, w tym choroby Parkinsona czy choroby Alzheimera. Wykazano także jego udział w patogenezie stwardnienia rozsianego. W związku z tym zwalczanie stresu oksydacyjnego stało się jednym z nowych celów terapeutycznych. W badaniach przedklinicznych i klinicznych oceniano skuteczność różnych substancji o właściwościach antyoksydacyjnych, m.in. polifenoli, witamin, kwasu α-liponowego czy ekstraktów z Ginkgo biloba, jako potencjalnych leków na stwardnienie rozsiane. Ich skuteczność w modelach zwierzęcych rzadko znajduje odzwierciedlenie w wynikach badań klinicznych, ale wybrane związki są obecnie w trakcie oceny klinicznej. W badaniach zarówno przedklinicznych, jak i klinicznych skuteczny okazał się fumaran dimetylu, zarejestrowany w 2013 roku do leczenia stwardnienia rozsianego. Mechanizm działania tego związku nie został jeszcze w pełni poznany. Wiadomo jednak, że pobudza on naturalny szlak antyoksydacyjny związany z czynnikiem transkrypcyjnym Nrf2, co prowadzi do redukcji nasilenia stresu oksydacyjnego.
Discipline
Year
Volume
16
Issue
3
Pages
136–145
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References
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