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J Alzheimers Dis ; 14(1): 85-93, 2008 May.
Article in English | MEDLINE | ID: mdl-18525130

ABSTRACT

Several studies suggested that the activity of erythrocyte Na,K-ATPase declines with aging. Here, it is postulated that alterations in the substrate kinetics of the erythrocyte membrane Na,K-ATPase could be more aggravated in conditions of brain cholinergic dysfunction seen in Alzheimer's disease than in normal aging. To test this hypothesis, we compared the Na,K-ATPase activity (Vmax/Km parameters) in aged rats with those in young rats with brain cholinergic dysfunction induced by electrolytic-, kainic acid-lesioned nucleus basalis magnocellularis (NBM) or by intracerebroventricular AlCl_{3} administration. In the above mentioned groups, Vmax values were significantly lower in comparison to the control animals. Furthermore, Km values were significantly higher in animals with electrolytic-induced NBM lesions, AlCl_{3} treated rats and aged animals. However, Km was significantly lower in kainic acid-induced NBM lesions compared to the control group. The Na,K-ATPase catalytic efficiency, estimated by the ratio Vm/Km, decreased as followed: young animals > aged animals > kainic acid lesion > electrolityc lesion > AlCl_{3}. Our data suggest that neurodegenerative processes similar to those seen in Alzheimer's disease affect the sodium/potassium pump functionality which might be detected in peripheral blood erythrocyte membranes.


Subject(s)
Aluminum Compounds/toxicity , Alzheimer Disease/enzymology , Basal Nucleus of Meynert/drug effects , Chlorides/toxicity , Disease Models, Animal , Erythrocyte Membrane/enzymology , Kainic Acid/toxicity , Sodium-Potassium-Exchanging ATPase/blood , Adenosine Triphosphate/blood , Age Factors , Aluminum Chloride , Animals , Basal Nucleus of Meynert/enzymology , Cholinergic Fibers/physiology , Injections, Intraventricular , Male , Potassium/blood , Rats , Rats, Wistar , Sodium/blood , Substrate Specificity
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