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Neurochemical Aspects of Amyotropic Lateral Sclerosis

Free fatty acid composition Altered Farooqui and Horrocks (2007) [Pg.278]

Other neurological diseases. It is proposed that anti-SGPG antibodies may be responsible for the activation of endothelial cells in ALS and the increased expression of E-selectin may be related to immunological disturbances in some ALS patients (Ikeda et ah, 2000). [Pg.280]

ALS occurs in sporadic and familial forms. The pathogenesis of neuronal degeneration in both sporadic and familial ALS may involve mutations in copper/zinc superoxide dismutase, mitochondrial dysfunction (alterations in respiratory complexes I and III), protein aggregation, and neuroinflammation (Aimer et al., 2001 Liu et al., 2002). Cytosolic Cu/Zn superoxide dismutase (SODl) is a ubiquitous small cytosolic metalloenzyme that catalyzes the conversion of superoxide anion to hydrogen peroxide. The mutant copper/zinc superoxide dismutase exhibits a toxic gain of function that adversely affects the function of neurons in the spinal cord, brain stem, and motor cortex. [Pg.280]


See other pages where Neurochemical Aspects of Amyotropic Lateral Sclerosis is mentioned: [Pg.278]    [Pg.281]    [Pg.283]   


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