Summary
Cytochemical techniques were used to demonstrate, with appropriate controls, alkaline phosphatase and HCO −3 -activated adenosine triphosphatase (ATPase) in rat duodenal brush border microvillus membranes. Intense activity of ecto-alkaline phosphatase activity was demonstrated with 2-glycerophosphate as substrate. Although biochemical assays suggested thatl-phenylalanine inhibited both alkaline phosphatase and HCO −3 -activated ATPase, cytochemical studies indicated that there was marked inhibition of alkaline phosphatase revealing a specific HCO −3 -activated ATPase on the inner aspect of the microvillus membrane. While it is tempting to suggest that this HCO −3 -activated ATPase is implicated in active bicarbonate secretion by the duodenum, decisive identification is not yet possible.
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Sharp, G., Stiel, D. & Peters, T.J. Cytochemical studies on the localization of alkaline phosphatase and HCO −3 -activated adenosine triphosphatase in the brush border membrane of rat duodenal enterocytes. Histochem J 15, 1131–1139 (1983). https://doi.org/10.1007/BF01003976
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DOI: https://doi.org/10.1007/BF01003976