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Cited by 233

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Furosemide inhibition of chloride transport in human red blood cells.

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Brazy, P C, Gunn, R B·1976·The Journal of general physiology

Abstract

The chloride self-exchange flux across the human red cell membrane is rapidly and reversibly inhibited by 10(-4) M furosemide, a potent chloruretic agent. Furosemide reduces the chloride flux at all chloride concentrations and increases the cellular chloride concentration at which the flux is half-maximum. Kinetic analysis of the flux measurements made at several furosemide and chloride concentrations yields a pattern of mixed inhibition with a dissociation constant for the inhibitor-transport mechanism complex of 5 X 10(-5) M. From this pattern of inhibition and other observations, including that the percent inhibition is independent of pH (range 5.6-8.9), we conclude that the anionic form of furosemide interacts primarily with the chloride transport mechanism at a site separate from both the transport site and the halide-reactive modifier site.

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Metadata

Authors
Brazy, P. C., & Gunn, R. B.
Venue
The Journal of general physiology
Published
1976-12-01
Volume
68
Issue
6
Pages
583-599
ISSN
  • 0022-1295 (ISSN-L)
  • 1540-7748
OpenAlex
W2116549996
Cited by
233
References
0
FWCI
4.95
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Furosemide inhibition of chloride transport in human red blood cells. https://app.cochat.ai/papers/10.1085/jgp.68.6.583
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Brazy, P. C., & Gunn, R. B. (1976). Furosemide inhibition of chloride transport in human red blood cells. The Journal of general physiology. https://doi.org/10.1085/jgp.68.6.583

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.