Evidence map›Paper›PMID 24647713›Full record

ReviewAmerican journal of physiology. Renal physiology2014

Ammonia transport in the kidney by Rhesus glycoproteins.

I David Weiner, Jill W Verlander

Abstract readReview
In one paragraph

Review in American journal of physiology. Renal physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 70 citations in OpenAlex.

  1. Uncoupling proximal tubule ammoniagenesis from bicarbonate generation byAmerican journal of physiology. Renal physiology · 2026
    Article
  2. Article
  3. Mechanistic insights into the liver-brain axis during chronic liver disease.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  4. Article
  5. Article
  6. State of knowledge on ammonia handling by the kidney.Pflugers Archiv : European journal of physiology · 2024
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. A mathematical model of the rat kidney. III. Ammonia transport.American journal of physiology. Renal physiology · 2021
    Article
  13. Testosterone modulates renal ammonia metabolism.American journal of physiology. Renal physiology · 2020
    Article
  14. NBCe1-A is required for the renal ammonia and KAmerican journal of physiology. Renal physiology · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Differences in renal ammonia metabolism in male and female kidney.American journal of physiology. Renal physiology · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

I David WeinerNephrology and Hypertension Section, North Florida/South Georgia Veterans Health System, Gainesville Florida; and Division of Nephrology, Hypertension, and Transplantation, University of Florida College of Medicine, Gainesville, Florida David.Weiner@Medicine.ufl.edu.
Jill W VerlanderNephrology and Hypertension Section, North Florida/South Georgia Veterans Health System, Gainesville Florida; and.
Florida College · USNorth Florida/South Georgia Veterans Health System · US

Funding

H/HCO3 transport in the collecting ductR01DK045788 · NIDDK · UNIVERSITY OF FLORIDA · PI WEINER, I. DAVID · 2000 to 2017
$4.4M
NIDDK NIH HHS R01 DK045788NIDDK NIH HHS R01-DK045788
6 · The paper itself

Abstract

Renal ammonia metabolism is a fundamental element of acid-base homeostasis, comprising a major component of both basal and physiologically altered renal net acid excretion. Over the past several years, a fundamental change in our understanding of the mechanisms of renal epithelial cell ammonia transport has occurred, replacing the previous model which was based upon diffusion equilibrium for NH3 and trapping of NH4(+) with a new model in which specific and regulated transport of both NH3 and NH4(+) across renal epithelial cell membranes via specific membrane proteins is required for normal ammonia metabolism. A major advance has been the recognition that members of a recently recognized transporter family, the Rhesus glycoprotein family, mediate critical roles in renal and extrarenal ammonia transport. The erythroid-specific Rhesus glycoprotein, Rh A Glycoprotein (Rhag), was the first Rhesus glycoprotein recognized as an ammonia-specific transporter. Subsequently, the nonerythroid Rh glycoproteins, Rh B Glycoprotein (Rhbg) and Rh C Glycoprotein (Rhcg), were cloned and identified as ammonia transporters. They are expressed in specific cell populations and membrane domains in distal renal epithelial cells, where they facilitate ammonia secretion. In this review, we discuss the distribution of Rhbg and Rhcg in the kidney, the regulation of their expression and activity in physiological disturbances, the effects of genetic deletion on renal ammonia metabolism, and the molecular mechanisms of Rh glycoprotein-mediated ammonia transport.

Indexed as

Acid-Base EquilibriumAmmoniaAnimalsBiological TransportCation Transport ProteinsGlycoproteinsHomeostasisHumansKidneyMembrane GlycoproteinsMembrane Transport ProteinsMiceModels, AnimalAmmoniaCation Transport ProteinsGlycoproteinsMembrane GlycoproteinsMembrane Transport ProteinsRHBG protein, humanRhBG protein, mouseRHCG protein, humanRhcg protein, mouseacid-baseammoniacollecting ductintercalated cellprincipal cell

Identifiers

PMID24647713
PMCPMC4024734
OpenAlexW2075736411

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.