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Sugar uptake into brush border vesicles from dog kidney. II. Kinetics
Biochimica Et Biophysica Acta
|August 17, 1978
Summary
Dog kidney cortex D-glucose transport involves both sodium-dependent and independent pathways. The sodium-dependent route shows high and low affinity sites, differing from alpha-methyl-D-glucoside transport kinetics.
Area of Science:
- Nephrology
- Molecular Biology
- Biochemistry
Background:
- D-glucose transport is crucial for kidney function.
- Understanding glucose transport kinetics aids in diagnosing and treating renal conditions.
Purpose of the Study:
- To investigate the kinetics of D-glucose transport in dog kidney cortex.
- To differentiate between sodium-dependent and independent transport mechanisms.
- To characterize the affinity and capacity of glucose transporters.
Main Methods:
- Vesiculated membrane preparation from dog kidney cortex.
- Uptake assays for D-glucose and alpha-methyl-D-glucoside.
- Eadie-Hofstee plot analysis to determine kinetic parameters.
- Investigation of effects of membrane potential and sodium gradients.
Main Results:
- D-glucose uptake exhibits both sodium-dependent and independent components.
- The sodium-dependent component is phlorizin-sensitive and electrogenic, with high and low affinity sites.
- alpha-Methyl-D-glucoside transport is sodium-dependent, phlorizin-sensitive, and shows a single carrier site kinetics.
- Newborn dog kidney shows similar kinetics, but with a less developed low-affinity system.
Conclusions:
- Dog kidney cortex utilizes distinct kinetic mechanisms for D-glucose and alpha-methyl-D-glucoside transport.
- The presence of high and low affinity sites for D-glucose suggests complex regulatory processes.
- Developmental differences in glucose transport systems are observed in newborn dogs.