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Malondialdehyde Contents in Infant Milk Formulas

Journal of Agricultural and Food Chemistry, 2004
Malondialdehyde (MDA) levels in infant milk formulas have been monitored by using an aqueous acid extraction method combined with the thiobarbituric acid method (TBA-test). Vegetable oils, with a remarkable content of polyunsaturated fatty acids (PUFA) are used to enrich the infant milk formulas. As PUFA are more susceptible to autoxidation, it becomes
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Glycosylation enhances malondialdehyde binding to proteins

Free Radical Biology and Medicine, 1996
To determine whether glycosylation of proteins increases their susceptibility to modification with malondialdehyde (MDA), bovine serum albumin, which was pretreated with 500 mg/dl dextrose at 37 degrees C for 0, 1, 2, and 4 weeks, were incubated with 100 mM MDA at 37 degrees C for 24 h.
A D, Mooradian, C C, Lung, J L, Pinnas
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Effect of malondialdehyde on nitrosamine formation

Food and Cosmetics Toxicology, 1980
Abstract Several aldehydes associated with foodstuffs were investigated for their effect on the formation of N-nitrosodimethylamine and N-nitrosodiethylamine. Whereas glucose, furfural, benzaldehyde and glyoxal had little influence on nitrosamine formation, malondialdehyde, which can be derived from lipids by peroxidation, greatly influenced the ...
T, Kurechi, K, Kikugawa, M, Ozawa
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Unique promotion of erythrophagocytosis by malondialdehyde

American Journal of Hematology, 1988
AbstractModification of the normal erythrocyte membrane by reagent malondialdehyde (MDA) promotes phagocytosis of red blood cells by human macrophages, a phenomenon previously shown to involve both IgG‐dependent and IgG‐independent mechanisms and to be demonstrable even at micromolar MDA concentrations.
R P, Hebbel, W J, Miller
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Serum Malondialdehyde in HIV Seropositive Children

Free Radical Biology and Medicine, 1998
Human immunodeficiency virus (HIV) infection is associated with oxidative stress as it has been demonstrated in adult seropositive individuals. We show in this study that serum malondialdehyde (MDA) concentration of HIV infected children was significantly higher than in control children. Moreover, a statistically significant decreased serum antioxidant
E J, Jareño   +4 more
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Malondialdehyde in Biological Systems

2019
Malondialdehyde (MDA) is one of several decomposition products of lipid peroxides formed in fats and oils, in food, and in the tissues. It is the most extensively investigated of these products because of its reactivity with a range of biological macromolecules and its association with the pathophysiology of a number of disease states.
H. H. Draper   +3 more
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Immunochemical properties of malondialdehyde-protein adducts

Journal of Immunological Methods, 1990
Malondialdehyde (MDA), a product of lipid peroxidation, can bind to and modify proteins by adduct formation. To determine whether MDA adducts were immunogenic, MDA was added to rabbit serum albumin (RSA) in order to characterize MDA-proteins and to immunize rabbits.
C C, Lung   +3 more
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Malondialdehyde Assays in Higher Plants

Malondialdehyde is a three-carbon dialdehyde produced as a byproduct of polyunsaturated fatty acid peroxidation widely used as a marker of the extent of lipid peroxidation in plants. There are several methodological approaches to quantify malondialdehyde contents in higher plants, ranging from the simplest, cheapest, and quickest spectrophotometric ...
Melanie, Morales, Sergi, Munné-Bosch
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Proinflammatory effects of malondialdehyde in lymphocytes

Journal of Leukocyte Biology, 2012
Abstract MDA changed cytokine/chemokines mRNA profiles in lymphocytes; increased cytokines expression is via oxidative stress, p38MAPK, and PKC pathways. Diabetes is an inflammatory disease promoted by alterations in immune cell function.
Somasundaram, Raghavan   +2 more
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An indo investigation of the structure and bonding in malondialdehyde and lithium malondialdehyde

Journal of Molecular Structure, 1975
Abstract The geometries of the enol forms of malondialdehyde and its lithium analog have been investigated using the INDO MO method in its original parametrization. The former molecule is predicted to have a planar, symmetric structure nearly identical with that of acetylacetone.
F.J. Marsh, B.G. Thomas, M.S. Gordon
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