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Stability of neuronal and glial marker enzymes in post-mortem rat brain
Authors:Terry Ritchie  Sheila A. Scully  Jean de Vellis  Ernest P. Noble
Affiliation:(1) Alcohol Research Center, University of California, 90024 Los Angeles, CA;(2) Department of Psychiatry and Biobehavioral Sciences, University of California, 90024 Los Angeles, CA;(3) Brain Research Institute, University of California, 90024 Los Angeles, CA;(4) Laboratory of Biomedical and Environmental Sciences, University of California, 90024 Los Angeles, CA;(5) Mental Retardation Research Center, University of California, 90024 Los Angeles, CA
Abstract:The enzymatic activities in post-mortem rat brain kept at 4°C and at 25°C were determined for a number of enzymes localized in specific cell types in the central nervous system. Choline acetyltransferase (CAT), glycerol-3-phosphate dehydrogenase (GPDH), glutamine synthetase (GS), lactate dehydrogenase (LDH) and 2prime,3prime-cyclic nucleotide phosphohydrolase (CNPase) were found to be very stable at both 4°C and 25°C with only slight, if any, losses of activity being seen even at periods as long as 72 hr. Glutamic acid decarboxylase (GAD) activity was less stable than that of the other enzymes. In brains kept at 4°C GAD activity was stable out to 24 hr after which it began to decline rapidly to 65% of control at 72 hr. In brains kept at 25°C, GAD activity was stable for 6–8 hr and then began to steadily decline to 58% of control at 24 hr and 29% of control at 72 hr. Assuming that these enzymes have similar stabilities in post-mortem human brain, the effect of post-mortem delay in processing tissues may be of lesser significance than other factors with regard to the measured enzyme activities in human brain samples.
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