Affiliations: Group of Neurobiology, Cardiology Research Center, Moscow, Russia | [x] Department of Biochemistry, M.V. Lomonosov Moscow State University, Moscow, Russia | [y] Department of Biomedical Sciences, Ohio University, Athens, OH, USA
Correspondence:
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Address for correspondence: Group of Neurobiology, Cardiology Research Center, 3-Cherepkovskaya st. 15A, Moscow, 121552, Russia. Tel.: +7 495 414 68 57; Fax: +7 495 414 66 99; E-mail: [email protected].
Abstract: The major cause of neurodegenerative disorders, including mid- to late-life onset Alzheimer's Disease, is permanent oxidative stress in the brain. Polyunsaturated fatty acids (PUFA) and α-tocopherol (α-TOH) are the most oxygen-sensitive constituents of cells. The presence of α-TOH in biological membranes is required but not sufficient to protect them against lipid peroxidation. The data presented in this review consider the role of α-TOH and cytochrome b5 which permit operation of lipid-radical cycles and the participation of lipid-radical reactions in key processes occurring in the membrane. Analysis of role of these cycles in membrane bioenergetics led us to a model involving the adenine nucleotide translocator and ATP synthesis in brain mitochondria. This paper summarizes experimental evidence for oxidative and non-oxidative pathways of PUFA metabolism with respective intermediates, which could be relevant to elucidation of new mechanisms of neurodegenerative diseases. Lipid-radical reactions in membranes work as important component of normal cell metabolism. Discussion is focused on the consequences of ineffective electron transfer to peroxyl radicals (LOO˙→ LOO-) and excessive oxidative pathway of PUFA metabolism (LOO˙→LOOH) with two reactive secondary products: malondialdehyde and methylglyoxal. Our future aim is to develop a more detailed model supplemented by the formation of lipofuscin and amyloid structures.
Keywords: Brain mitochondria, ATP synthesis, cytochrome b5, α-tocopherol, methylglyoxal
