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The Journal of veterinary medical science1993; 55(2); 281-285; doi: 10.1292/jvms.55.281

A novel response of anion transporter in equine erythrocytes to a fluorescent substrate, N-(2-aminoethyl sulfonate)-7-nitrobenz-2-oxa-3-diazole (NBD-taurine).

Abstract: This report describes a unique response of the anion transporter in equine erythrocytes to the fluorescent substrate N-(2-aminoethyl sulfonate)-7-nitrobenz-2-oxa-3-diazole (NBD-taurine). Equine erythrocytes showed fluxes of NBD-taurine both inward and outward at rates considerably slower than those in human cells. These fluxes were completely abolished by a typical anion transport inhibitor, 4,4'-diisothiocyanostilbene-2,2'-disulfonate. Furthermore, NBD-taurine competitively inhibited the uptake of phosphate in equine red cells with an inhibition constant of phosphate that was slightly higher than the Michaelis constant of phosphate uptake. These results demonstrate that the anion transporter (band 3) in equine red cells binds NBD-taurine but does not prefer it as the substrate for transport, suggesting a structural difference between equine and human anion transporters at the polypeptide portion which is implicated in anion transport.
Publication Date: 1993-04-01 PubMed ID: 8513010DOI: 10.1292/jvms.55.281Google Scholar: Lookup
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  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research study investigates how the anion transporter in horse red blood cells responds to a fluorescent substrate, called NBD-taurine, showing distinctive reactions compared to human cells, suggesting a fundamental structural difference between equine and human anion transporters.

Introduction to the Research

  • The paper seeks to understand the unique reaction of the anion transporter (specifically, band 3) in equine erythrocytes (horse red blood cells) to a fluorescent substrate named NBD-taurine.
  • Scientists have found that equine erythrocytes demonstrate influxes and outflows of NBD-taurine at rates much slower than those observed in human cells.
  • The study aims to examine why this difference exists and what implications it could have on our understanding of anion transporters.

Experimental Research and Findings

  • The rates of NBD-taurine flowing in and out were completely stopped by a common anion transport inhibitor, 4,4′-diisothiocyanostilbene-2,2′-disulfonate, indicating that these fluxes do involve the anion transporter.
  • The research paper also noted that NBD-taurine competitively inhibited the uptake of phosphate in equine red cells. The inhibition constant of phosphate was slightly higher than its Michaelis constant, which defines the rate of uptake.
  • Interestingly, the study found that band 3 in equine red cells binds NBD-taurine but doesn’t seem to prefer it as a substrate for transport. This suggests a structural difference between equine and human anion transporters, specifically at the polypeptide part, which is responsible for anion transport.

Significance and Impact of the Research

  • The research provides a fresh perspective on the structural differences of anion transporters between species – horses and humans in this case.
  • It furthers our understanding of how various species’ erythrocytes (red blood cells) function under specific substrates or inhibitors and opens new paths for research related to equine blood cells and the role of anion transporters.
  • Such studies could aid in developing better medications and treatments for diseases in both animals and humans that involve anion transportation in the erythrocytes.

Cite This Article

APA
Inaba M, Goto I, Sato K, Maede Y. (1993). A novel response of anion transporter in equine erythrocytes to a fluorescent substrate, N-(2-aminoethyl sulfonate)-7-nitrobenz-2-oxa-3-diazole (NBD-taurine). J Vet Med Sci, 55(2), 281-285. https://doi.org/10.1292/jvms.55.281

Publication

ISSN: 0916-7250
NlmUniqueID: 9105360
Country: Japan
Language: English
Volume: 55
Issue: 2
Pages: 281-285

Researcher Affiliations

Inaba, M
  • Department of Veterinary Internal Medicine, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Goto, I
    Sato, K
      Maede, Y

        MeSH Terms

        • Animals
        • Biological Transport
        • Carrier Proteins / blood
        • Carrier Proteins / drug effects
        • Erythrocytes / drug effects
        • Erythrocytes / metabolism
        • Fluorescent Dyes
        • Horses / blood
        • Humans
        • Kinetics
        • Oxadiazoles / blood
        • Oxadiazoles / pharmacology
        • Phosphate-Binding Proteins
        • Phosphates / blood
        • Species Specificity
        • Taurine / analogs & derivatives
        • Taurine / blood
        • Taurine / pharmacology

        Citations

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