Evidence map›Paper›PMID 17890869›Full record

ArticleKidney & blood pressure research2007

Combined effects of carbonic anhydrase inhibitor and adenosine A1 receptor antagonist on hemodynamic and tubular function in the kidney.

Cynthia M Miracle, Timo Rieg, Roland C Blantz, Volker Vallon, Scott C Thomson

Open access · bronzeAbstract read
In one paragraph

Article in Kidney & blood pressure research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Contribution of NHE3 and dietary phosphate to lithium pharmacokinetics.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2019
    Article
  2. Article
  3. Caffeine-induced diuresis and natriuresis is independent of renal tubular NHE3.American journal of physiology. Renal physiology · 2015
    Article
  4. Article
  5. Article
  6. Acute and chronic effects of SGLT2 blockade on glomerular and tubular function in the early diabetic rat.American journal of physiology. Regulatory, integrative and comparative physiology · 2012 · on this map
    Article
  7. Article
  8. Article
  9. Adenosine receptors and the kidney.Handbook of experimental pharmacology · 2009
    Review
  10. Review
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

5 authors at 1 institution in 1 country.

Cynthia M MiracleDivision of Nephrology-Hypertension, University of California, Veterans Affairs San Diego Healthcare System, San Diego, CA 92161, USA. cmiracle@ucsd.edu
Timo Rieg
Roland C Blantz
Volker Vallon
Scott C Thomson
VA San Diego Healthcare System · US

Funding

AUTOREGULATION OF GLOMERULAR FILTRATION RATER01DK028602 · NIDDK · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI BLANTZ, ROLAND C · 1986 to 2011
$3.9M
NIDDK NIH HHS R01 DK028602NIDDK NIH HHS R01 DK-28602NIDDK NIH HHS T32 DK0076711-11
6 · The paper itself

Abstract

backgroundCarbonic anhydrase inhibitors (CAI) reduce proximal reabsorption, activating tubuloglomerular feedback (TGF) and reducing glomerular filtration rate (GFR). Adenosine A(1) receptors (A(1)R) mediate the TGF response and stimulate proximal reabsorption.

methodsClearance and micropuncture studies were performed in Wistar rats to determine whether blockade of A(1)R (KW3902 0.3 mg/kg i.v.) would prevent CAI (benzolamide 5 mg/kg i.v.) from lowering GFR, whether CAI and KW3902 exert additive effects on sodium excretion, and to what extent such interactions depend on events in the glomerulus, proximal tubule, or distal nephron.

resultsKW3902 raised GFR and prevented CAI from lowering GFR. KW3902 and CAI caused additive diuresis and natriuresis. KW3902 and CAI increased lithium clearance, but their effects were redundant. CAI increased the dependence of proximal reabsorption on active chloride transport. KW3902, alone, did likewise, but to a lesser extent than CAI. Adding KW3902 to CAI lessened the shift toward active chloride transport.

conclusionsThe data reveal that A(1)R mediate glomerular vascular resistance whether or not TGF is activated, that additive effects of CAI and KW3902 on salt excretion occur, in part, because KW3902 inhibits reabsorption downstream from the macula densa, and that KW3902 likely inhibits proximal reabsorption by interfering with apical sodium-hydrogen exchange.

Indexed as

Adenosine A1 Receptor AntagonistsAnimalsBenzolamideCarbonic Anhydrase InhibitorsDiureticsDrug SynergismGlomerular Filtration RateHeart RateKidney TubulesLithiumMaleRatsRats, WistarRegional Blood FlowSodiumVasoconstrictionAdenosine A1 Receptor AntagonistsBenzolamideCarbonic Anhydrase InhibitorsDiureticsLithiumrolofyllineSodiumXanthines

Identifiers

PMID17890869
PMCPMC2814144
OpenAlexW2010080463

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.