Abstract
Prior studies demonstrated far greater amounts of lipid peroxidation (LP) in mitochondria from the zona reticularis (inner zone) of the guinea pig adrenal cortex than in mitochondria from the outer zone (zona fasciculata + zona glomerulosa) of the gland. α-Tocopherol concentrations, by contrast, were greater in the outer zone. To determine if the differences in α-tocopherol content were responsible for the regional differences in LP, the effects of α-tocopherol deficiency on mitochondrial LP were investigated. Tocopherol deficiency had relatively little effect on ferrous ion- or ascorbic acid-induced LP in inner zone mitochondria. However, depletion of adrenal tocopherol substantially increased outer zone LP, eliminating the differences between the two zones. Fatty acid analyses revealed that mitochondria from tocopherol-deficient animals contained significantly less linoleic acid (C18 : 2) and arachidonic acid (C20:4) than those from controls, suggesting peroxidative losses in vivo. In mitochondria from control animals, subphysiological concentrations of ascorbic acid stimulated LP, but physiological levels did not. However, in tocopherolepleted mitochondria, even physiological concentrations of ascorbic acid stimulated LP. The results indicate that the intra-adrenal distribution of α-tocopherol is responsible for the regional differences in mitochondrial LP and that α-tocopherol is a major determinant of ascorbic acid actions on adrenal LP. The data also provide evidence of adrenal LP in vivo in tocopherol-deficient animals.
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