The Open Toxicology Journal




(Discontinued)

ISSN: 1874-3404 ― Volume 7, 2021

Role of Environmental and Inflammatory Toxicity in Neuronal Cell Death


The Open Toxicology Journal , 2008, 2: 26-41

Mallika Somayajulu-Nitu, Danijela Domazet-Damjanov, Anca Matei, Edward Schwartzenberger, Jerome Cohen , Siyaram Pandey

Chemistry and Biochemistry, University of Windsor, Windsor, ON N9B 3P4, Canada.

Electronic publication date 04/7/2008
[DOI: 10.2174/1874340400802010026]




Abstract:

Neuronal cells are exclusively dependent on oxidative phosphorylation for energy and are under constant threat of oxidative damage due to mitochondrial production of reactive oxygen species by partial reduction of molecular oxygen. These cells also have a multitude of antioxidative defense mechanisms, but there is a slow decline of antioxidative defence capacity with aging. The result is the increased vulnerability of cells to oxidative stress, particularly neuronal cells. Any environmental, inflammatory or psychological stress that can topple the redox balance will eventually lead to oxidative stress and neuronal cell death. Indeed, cell death induced by oxidative stress has been implicated in age-related loss of neurons during normal aging and several neurodegenerative disorders. It is critical to understand the mechanisms by which different risk factors lead to neuronal cell death in order to identify pathways involved in neurodegenerative diseases. In this review we focus on the implications of various factors such as environmental toxins, drugs and psychological stress in neurodegenerative diseases with specific focus on Parkinson’s disease and Alzheimer’s disease. Here we highlight the recent progress that supports the role of molecular mechanisms of oxidative stress, neuroinflammation and mitochondrial dysfunction as contributors to neurotoxicity and research on developing therapeutics that could potentially slow down the progression of neurodegeneration.


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