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1.
Cell Immunol ; 263(2): 166-71, 2010.
Article in English | MEDLINE | ID: mdl-20392440

ABSTRACT

Altered neutrophil function may contribute to the development of AIDS during the course of HIV infection. It has been described that Nef, a regulatory protein from HIV, can modulate superoxide production in other cells, therefore altered superoxide production in neutrophils from HIV infected patients, could be secondary to a direct effect of Nef on components of the NADPH oxidase complex. In this work, we describe that Nef, was capable of increasing superoxide production in human neutrophils. Furthermore, a specific association between Nef and p22-phox, a membrane component of the NADPH oxidase complex, was found. We propose that this association may reflect a capability of Nef to modulate by direct association, the enzymatic complex responsible for one of the most efficient innate defense mechanisms in phagocytes, contributing to the pathogenesis of the disease.


Subject(s)
HIV-1/metabolism , NADH, NADPH Oxidoreductases/metabolism , NADPH Oxidases/metabolism , nef Gene Products, Human Immunodeficiency Virus/metabolism , Cloning, Molecular , Flow Cytometry , Fluorescent Antibody Technique , HIV-1/pathogenicity , Humans , Multienzyme Complexes , NADPH Oxidase 1
2.
Neurosci Lett ; 327(3): 149-52, 2002 Jul 26.
Article in English | MEDLINE | ID: mdl-12113899

ABSTRACT

There is evidence that systemic administration of haloperidol, a dopamine receptor blocker, attenuates visual cortex evoked potentials. However, there is scarce information on cortical neurochemical changes associated with haloperidol effects on visual function. The present experiment was designed to investigate: (1) the effect of photic stimulation on glutamate release in the visual cortex; and (2) whether systemic administration of haloperidol would affect those neurochemical changes. Microdialysis probes were implanted in the occipital cortex. Glutamate levels were measured every 30 s using capillary zone electrophoresis. Extracellular glutamate levels increased to about 282% 30 s after photic stimulation started and remain elevated for the 3 min that the photic stimulation lasted. Haloperidol (1.5 and 5 mg/kg, i.p.) completely suppressed the increased of glutamate efflux during photic stimulation. Finally, it was also found that the highest dose of haloperidol (5 mg/kg) did not change glutamate basal levels. The results are discussed with reference to possible dopaminergic actions on the visual system function.


Subject(s)
Dopamine Antagonists/pharmacology , Glutamic Acid/metabolism , Haloperidol/pharmacology , Photic Stimulation , Visual Cortex/drug effects , Visual Cortex/metabolism , Animals , Electrophoresis , Extracellular Space/drug effects , Extracellular Space/metabolism , Glutamic Acid/drug effects , Male , Microdialysis , Rats , Rats, Wistar
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