Glucose transport by horse kidney brush borders. I.–Transport properties of brush border membrane closed vesicles.
Abstract: Brush border membranes isolated from horse kidney cortex as closed right-side out vesicles show selective permeability when analyzed on sucrose and dextran gradients. These vesicles can actively accumulate D-glucose. The preservation of the glucose transport system is demonstrated by the following features: (a) the uptake and release rates of D-glucose are higher in the presence of a sodium gradient, showing that D-glucose transport is a sodium-dependent process; (b) this transport, specific for the D-isomer, is inhibited by phlorizin; (c) the D-glucose transport system is saturable; (d) no inhibition of D-glucose transport is found with C-mannose; (e) the D-glucose uptake is sensitive to osmotic variations.
Publication Date: 1978-09-29 PubMed ID: 719044DOI: 10.1016/s0300-9084(78)80783-4Google Scholar: Lookup
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- Journal Article
Summary
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This research analyzed the transport characteristics of glucose across the brush border membranes of horse kidneys. It demonstrates that these membranes carry out selective, sodium-dependent glucose transport that can be inhibited by phlorizin and is sensitive to osmotic changes.
Methodology and Findings
- The membranes in question were isolated from the cortex of a horse kidney and established as closed right-side out vesicles. These vesicles were found to have selective permeability when tested on sucrose and dextran gradients.
- The glucose transport process was observed and verified by several measures. The vesicles were found to actively accumulate D-glucose, signifying an efficient glucose transport system.
The Transport Process: Characteristics and Effectors
- The rate of uptake and release of D-glucose was found to be higher when a sodium gradient was present, indicating that the D-glucose transport is sodium-dependent. This suggests that sodium ions may play a crucial role in facilitating the transport mechanism.
- D-glucose transport was found to be specific for the D-isomer. Phlorizin, a known inhibitor of glucose transport in the kidneys, was found to impede this transport process, providing further evidence of the mechanism’s function.
- The transportation system showcased saturation kinetics, meaning there’s a maximum rate at which glucose can be transported over time, even with increased glucose concentration.
- The study also found that C-mannose, a stereoisomer of glucose, did not inhibit D-glucose transport, suggesting that the carrier protein involved in the transport is highly specific and does not interact with similar but structurally different sugars.
- Lastly, the researchers discovered the D-glucose uptake is sensitive to osmotic variations, meaning the transport can be affected by changes in pressure or concentration of other particles in the solution.
Cite This Article
APA
Poirée JC, Vannier C, Sudaka P, Fehlmann M.
(1978).
Glucose transport by horse kidney brush borders. I.–Transport properties of brush border membrane closed vesicles.
Biochimie, 60(6-7), 645-651.
https://doi.org/10.1016/s0300-9084(78)80783-4 Publication
Researcher Affiliations
MeSH Terms
- Animals
- Biological Transport, Active / drug effects
- Carbohydrates / pharmacology
- Cell Membrane / metabolism
- Cell Membrane Permeability / drug effects
- Glucose / metabolism
- Horses
- In Vitro Techniques
- Kidney Cortex / metabolism
- Kidney Cortex / ultrastructure
- Microvilli / metabolism
- Osmotic Pressure
- Phlorhizin / pharmacology
- Sodium / pharmacology
Citations
This article has been cited 4 times.- Meier A, Reiche D, de Laat M, Pollitt C, Walsh D, Sillence M. The sodium-glucose co-transporter 2 inhibitor velagliflozin reduces hyperinsulinemia and prevents laminitis in insulin-dysregulated ponies.. PLoS One 2018;13(9):e0203655.
- Mengual R, Sudaka P. The mechanism of Na+-L-lactate cotransport by brush border membrane vesicles from horse kidney: analysis of rapid equilibrium kinetics in absence of membrane potential.. J Membr Biol 1983;71(3):163-71.
- Boudouard M, Giudicelli J, Vannier C, Sudaka P. Reconstitution of brush border membrane proteins in phosphatidylcholine vesicles. Biochemical and functional characterization.. Biochem J 1986 Apr 1;235(1):111-6.
- Mengual R, Claude-Schlageter MH, Poiree JC, Yagello M, Sudaka P. Characterization of sodium and pyruvate interactions of the two carrier systems specific of mono- and di- or tricarboxylic acids by renal brush-border membrane vesicles.. J Membr Biol 1989 Jun;108(3):197-205.
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