Evidence map›Paper›PMID 10981146›Full record

ReviewCurrent hypertension reports2000

Renal dopamine and sodium homeostasis.

P A Jose, G M Eisner, R A Felder

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Current hypertension reports, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00685919 (Kidney Dopamine Effects on Urinary Sodium Excretion in Postural Tachycardia Syndrome), which is not on this map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.7field-weighted citation impact, top 31% 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.

NCT00685919 phase2 / phase3completednot on this mapstarted 2008, after this paper: background citation

Kidney Dopamine Effects on Urinary Sodium Excretion in Postural Tachycardia Syndrome

TypeinterventionalSponsorVanderbilt UniversityRan2008 to 2021Enrolled32ConditionsPostural Tachycardia Syndrome, Orthostatic IntoleranceArmsCarbidopa, Placebo
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. The Intricacies of Renal Phosphate Reabsorption-An Overview.International journal of molecular sciences · 2024
    Review
  3. Dopamine reduces cell surface NaAmerican journal of physiology. Renal physiology · 2017
    Article
  4. Article
  5. Article
  6. Article
  7. NHERF-1 and the regulation of renal phosphate reabsoption: a tale of three hormones.American journal of physiology. Renal physiology · 2012
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Effects of long-term ouabain treatment on blood pressure, sodium excretion, and renal dopamine D(1) receptor levels in rats.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2010
    Article
  13. Article
  14. Inhibition of natriuretic factors increases blood pressure in rats.American journal of physiology. Renal physiology · 2009
    Article
  15. Article
  16. Dopamine receptors and hypertension.Current hypertension reports · 2008
    Review
  17. Article
  18. Article
  19. Dopamine receptor-coupling defect in hypertension.Current hypertension reports · 2002
    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

3 authors at 2 institutions in 1 country.

P A JoseDepartment of Pediatrics, Georgetown University Medical Center, 3800 Reservoir Road NW, Washington, DC 20007, USA.
G M Eisner
R A Felder
Georgetown University · USUniversity of Virginia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the past decade, it has become evident that dopamine plays an important role in the regulation of fluid and electrolyte balance and blood pressure. Dopamine exerts its actions through two families of dopamine receptors, designated D1-like and D2-like, which are identical in the brain and in peripheral tissues. The two D1-like receptors--D1 and D5 receptors--expressed in mammals are linked to stimulation of adenylyl cyclase. The three D2-like receptors--D2, D3, and D4,--are linked to inhibition of adenylyl cyclase. Dopamine affects fluid and electrolyte balance by regulation of renal excretion of electrolytes and water through actions on renal hemodynamics and tubular epithelial transport and by modulation of the secretion and/or action of vasopressin, renin, aldosterone, catecholamines, and endothelin B receptors (ETB) receptors. It also affects fluid and sodium intake by way of "appetite" centers in the brain and alterations of gastrointestinal tract transport. The production of dopamine in neural and non-neural tissues and the presence of receptors in these tissues suggest that dopamine can act in an autocrine or paracrine fashion. This renal autocrine-paracrine function, which becomes most evident during extracellular fluid volume expansion, is lost in essential hypertension and in some animal models of genetic hypertension. This deficit may be caused by abnormalities in renal dopamine production and polymorphisms or abnormal post-translational modification and regulation of dopamine receptor subtypes.

Indexed as

Adenylyl CyclasesAnimalsBiological Transport, ActiveDopamineHomeostasisHumansHypertensionKidneyNatriuresisReceptors, DopamineSodiumWater-Electrolyte BalanceAdenylyl CyclasesDopamineReceptors, DopamineSodium

Identifiers

PMID10981146
OpenAlexW2015522286

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.