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Journal ArticleDOI

Oxidative stress in autism

Abha Chauhan, +1 more
- 01 Aug 2006 - 
- Vol. 13, Iss: 3, pp 171-181
TLDR
Increases in oxidative stress with membrane lipid abnormalities, inflammation, aberrant immune response, impaired energy metabolism and excitotoxicity, leading to clinical symptoms and pathogenesis of autism is proposed.
About
This article is published in Pathophysiology.The article was published on 2006-08-01. It has received 569 citations till now. The article focuses on the topics: Autism & Oxidative stress.

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Citations
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Journal ArticleDOI

From Genes to Environment: Using Integrative Genomics to Build a “Systems-Level” Understanding of Autism Spectrum Disorders

TL;DR: Emphasis is placed on the need to study defined ASD phenotypes as well as to integrate large-scale "omics" data in order to develop a "systems-level" perspective of ASD, which in turn is necessary to allow predictions regarding responses to specific perturbations and interventions.
Journal ArticleDOI

Homocysteine level in urine of autistic and healthy children.

TL;DR: The higher level of homocysteine in autistic children may indicate deficiencies of folic acid and vitamins B ₆ and B₁₂ in nutrition of these children.
Journal ArticleDOI

Altered Sulfur Amino Acid Metabolism In Immune Cells of Children Diagnosed With Autism

TL;DR: A novel liquid chromatography linked tandem mass spectrometric method was used to determine the levels of SAA metabolites in peripheral blood mononuclear cells obtained from 11 healthy controls and 31 autistic children, providing novel evidence for altered metabolism in immune cells.
Journal ArticleDOI

Malondialdehyde, Bcl-2, Superoxide Dismutase and Glutathione Peroxidase may Mediate the Association of Sonic Hedgehog Protein and Oxidative Stress in Autism

TL;DR: The level or activity of Bcl-2, brain-derived neurotrophic factor, and the activities of superoxide dismutase and glutathione peroxidase are decreased in autism.
Journal ArticleDOI

Alterations of circulating endogenous secretory RAGE and S100A9 levels indicating dysfunction of the AGE-RAGE axis in autism.

TL;DR: The results of a significantly reduced peripheral level of esRAGE coupled with elevated S100A9 point to a subtle but definite dysfunction of the AGEs/RAGE axis in autism that could play a role in the pathophysiology of this disorder.
References
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Book ChapterDOI

Role of free radicals and catalytic metal ions in human disease: an overview.

TL;DR: The chapter discusses the metabolism of transition metals, such as iron and copper, and the chelation therapy that is an approach to site-specific antioxidant protection.
Journal ArticleDOI

Nitric oxide: a cytotoxic activated macrophage effector molecule.

TL;DR: The results suggest that nitric oxide is the precursor of nitrite/nitrate synthesized by cytotoxic activated macrophages and, via formation of iron-nitric oxide complexes and subsequent degradation of Iron-sulfur prosthetic groups, an effector molecule.
Journal ArticleDOI

The mitochondrial death/life regulator in apoptosis and necrosis

TL;DR: The acquisition of the biochemical and ultrastructural features of apoptosis critically relies on the liberation of apoptogenic proteases or protease activators from mitochondria.
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Neuroglial activation and neuroinflammation in the brain of patients with autism

TL;DR: It is indicated that innate neuroimmune reactions play a pathogenic role in an undefined proportion of autistic patients, suggesting that future therapies might involve modifying neuroglial responses in the brain.
Journal ArticleDOI

Biological effects of the superoxide radical.

TL;DR: Can the superoxide radical exert deleterious effects independent of participating with H2O2 in the production of the hydroxyl radical?
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