International Meeting for Autism Research (May 7 - 9, 2009): Increased Activities of Brain Na+-K+-ATPase and Ca2+-Mg2+-ATPase in Frontal Cortex and Cerebellum from Autism

Increased Activities of Brain Na+-K+-ATPase and Ca2+-Mg2+-ATPase in Frontal Cortex and Cerebellum from Autism

Thursday, May 7, 2009
Northwest Hall (Chicago Hilton)
10:00 AM
V. Chauhan , Neurochemistry, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, NY
L. Ji , Neurochemistry, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, NY
B. Muthiayah , Neurochemistry, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, NY
W. T. Brown , Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY
A. Chauhan , Neurochemistry, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, NY
Background: The enzymes Na+-K+-ATPase and Ca2+-Mg2+-ATPase are ubiquitously present and they maintain intracellular gradients of ions that are essential for signal transduction. 

Objectives: To compare the activities of Na+-K+-ATPase and Ca2+-Mg2+-ATPase in brain homogenates from frontal, temporal, parietal, and occipital cortex and cerebellum from autism subjects with an age range of 4 to 39 yrs (N = 7 to 10 for different regions) and age-matched control subjects (N = 9 to 10). 

Methods: Na+-K+-ATPase and Ca2+-Mg2+-ATPase hydrolyze the ATP into ADP and inorganic phosphorus.  Inorganic phosphorus thus released was assayed by measuring the inorganic phosphorus.

Results: The activities of both Na+-K+-ATPase (p < 0.05) and Ca2+-Mg2+-ATPase (p < 0.001) were significantly increased in the cerebellum in the autism samples as compared to age-matched controls. The activity of Na+-K+-ATPase (p < 0.05) but not Ca2+-Mg2+-ATPase was increased in the frontal cortex in the autism samples as compared to age-matched controls.  In contrast, the activities of these enzymes were not different between autism and control groups in other regions of brains, i.e., temporal, parietal and occipital cortex.  
Conclusions: We propose that increased activities of Na+-K+-ATPase and Ca2+-Mg2+-ATPase in frontal cortex and cerebellum may contribute, in part, to altered neocortical circuit functions in autism.

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