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2.
Neurosci Lett ; 405(1-2): 89-93, 2006 Sep 11.
Article in English | MEDLINE | ID: mdl-16854526

ABSTRACT

Nitric oxide (NO) is a physiological neurotransmitter, a mediator of the excitatory neurotransmitter glutamate pathways that regulates several neuroendocrine functions, but excessive NO is toxic by itself and it interacts with superoxide radical (O(2)(-)) to form the peroxynitrite anion (ONOO(-)). Using rat brain homogenates, we investigated the effects of melatonin and pinoline in preventing the level of lipid peroxidation (LPO) and carbonyl contents in proteins induced by nitric oxide (NO) which was released by the addition of sodium nitroprusside (SNP). Lipid and protein peroxidation were estimated by quantifying malondialdehyde (MDA) and 4-hydroxyalkenal (4-HDA) concentrations and carbonyl contents, respectively. SNP increased MDA+4-HDA and carbonyl contents production in brain homogenates in a time and concentration dependent manner. Both, melatonin and pinoline reduced NO-induced LPO and carbonyl contents in a dose-dependent manner in concentrations from 0.03 to 3 mM and 1 to 300 microM, respectively. Under the in vitro conditions of this experiment, both antioxidants were more efficient in limiting SNP protein oxidation than lipid damage.


Subject(s)
Antioxidants/metabolism , Brain/metabolism , Carbolines/metabolism , Lipid Peroxidation , Melatonin/metabolism , Nitric Oxide/physiology , Protein Carbonylation , Animals , Antioxidants/pharmacology , Carbolines/pharmacology , In Vitro Techniques , Lipid Peroxidation/drug effects , Male , Melatonin/pharmacology , Nitric Oxide Donors/pharmacology , Nitroprusside/pharmacology , Peroxides/metabolism , Protein Carbonylation/drug effects , Rats , Rats, Sprague-Dawley
3.
J Trace Elem Med Biol ; 19(1): 19-22, 2005.
Article in English | MEDLINE | ID: mdl-16240667

ABSTRACT

According to the Fluid Mosaic Model, a biological membrane is a two-dimensional fluid of oriented proteins and lipids. The lipid bilayer is the basic structure of all cell and organelle membranes. Cell membranes are dynamic, fluid structures, and most of their molecules are able to move in the plane of the membrane. Fluidity is the quality of ease of movement and represents the reciprocal value of membrane viscosity. Fluid properties of biological membranes are essential for numerous cell functions. Even slight changes in membrane fluidity may cause aberrant function and pathological processes. Several evidences suggest that trace elements, e.g., iron, copper, zinc, selenium, chromium, cadmium, mercury and lead may influence membrane fluidity. The interaction of heavy metals with cellular membranes may contribute to explain, at least partially, the toxicity associated with these metals.


Subject(s)
Cell Membrane/chemistry , Membrane Fluidity , Trace Elements/chemistry , Cell Membrane/metabolism , Free Radicals/chemistry , Lipid Peroxidation
4.
Neurosci Lett ; 323(1): 55-9, 2002 Apr 19.
Article in English | MEDLINE | ID: mdl-11911989

ABSTRACT

Deferoxamine (DF) is an antioxidant molecule because of its ability to chelate iron. This study compared the ability of DF alone or in combination with melatonin, 5-methoxytryptophol or pinoline in preventing lipid peroxidation due to hydrogen peroxide (H(2)O(2)) in rat brain homogenates. Malondialdehyde (MDA) and 4-hydroxyalkenals (4-HDA) in the homogenates were measured as indices of lipid peroxidation. Incubation of homogenates with DF reduced, in a dose-dependent manner, MDA+4-HDA formation due to H(2)O(2). When melatonin, 5-methoxytryptophol or pinoline were added to the incubation medium, the efficacy of DF in preventing lipid peroxidation was enhanced. These cooperative effects between DF, melatonin, and related pineal products may be important in protecting tissues from the oxidative stress due to iron overload.


Subject(s)
Antioxidants/pharmacology , Brain/drug effects , Brain/metabolism , Deferoxamine/pharmacology , Hydrogen Peroxide/adverse effects , Iron Chelating Agents/pharmacology , Lipid Peroxidation/drug effects , Melatonin/pharmacology , Animals , Hydrogen Peroxide/pharmacology , Male , Malondialdehyde/metabolism , Rats , Rats, Sprague-Dawley
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