Evidence map›Paper›PMID 23213191›Full record

ArticleHypertension (Dallas, Tex. : 1979)2013

Central nervous system Gαi2-subunit proteins maintain salt resistance via a renal nerve-dependent sympathoinhibitory pathway.

Daniel R Kapusta, Crissey L Pascale, Jill T Kuwabara, Richard D Wainford

Open access · bronzeAbstract read
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Central GαiFrontiers in endocrinology · 2022
    Review
  6. Salt sensitivity and hypertension.Journal of human hypertension · 2021
    Review
  7. Article
  8. Neuroanatomical characterization of GαiPhysiological genomics · 2021
    Article
  9. Sensory Afferent Renal Nerve Activated GαiFrontiers in physiology · 2021
    Article
  10. Article
  11. Hypothalamic Paraventricular Nucleus GαiHypertension (Dallas, Tex. : 1979) · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Mechanisms of altered renal sodium handling in age-related hypertension.American journal of physiology. Renal physiology · 2018
    Review
  17. Article
  18. Review
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Daniel R KapustaDepartment of Pharmacology and Experimental Therapeutics and the Whitaker Cardiovascular Institute, Boston University School of Medicine, 72 E Concord St, Boston, MA 02118, USA.
Crissey L Pascale
Jill T Kuwabara
Richard D Wainford
Boston University · US

Funding

VASCULAR SMOOTH MUSCLE PLASTICITY IN NITRIC OXIDEP20RR018766 · NCRR · LSU HEALTH SCIENCES CENTER · PI KAPUSTA, DANIEL R · 2003 to 2011
$18.5M
MENTORING IN CARDIOVASCULAR BIOLOGYP20GM103514 · NIGMS · LSU HEALTH SCIENCES CENTER · PI KAPUSTA, DANIEL R · 2012 to 2012
$2.0M
Brain G-alpha subunit protein mediated neural control of blood pressureR01HL107330 · NHLBI · LSU HEALTH SCIENCES CENTER · PI WAINFORD, RICHARD DAVID · 2011 to 2015
$1.9M
NCRR NIH HHS P20 RR018766NHLBI NIH HHS HL-107330NHLBI NIH HHS R01 HL107330NIGMS NIH HHS 8P20 GM103514NIGMS NIH HHS P20 GM103514
6 · The paper itself

Abstract

In salt-resistant phenotypes, chronic elevated dietary sodium intake evokes suppression of renal sodium-retaining mechanisms to maintain sodium homeostasis and normotension. We have recently shown that brain Gαi(2) protein pathways are required to suppress renal sympathetic nerve activity and facilitate maximal sodium excretion during acute intravenous volume expansion in Sprague-Dawley rats. Here, we studied the role of brain Gαi(2) proteins in the endogenous central neural mechanisms acting to maintain fluid and electrolyte homeostasis and normotension during a chronic elevation in dietary salt intake. Naive or bilaterally renal denervated adult male Sprague-Dawley rats were randomly assigned to receive an intracerebroventricular scrambled or Gαi(2) oligodeoxynucleotide infusion and then subjected to either a normal salt (0.4%) or high-salt (8.0%) diet for 21 days. In scrambled oligodeoxynucleotide-infused rats, salt loading, which did not alter blood pressure, evoked a site-specific increase in hypothalamic paraventricular nucleus Gαi(2) protein levels and suppression of circulating norepinephrine content and plasma renin activity. In salt-loaded rats continuously infused intracerebroventricularly with a Gαi(2) oligodeoxynucleotide, animals exhibited sodium and water retention, elevated plasma norepinephrine levels, and hypertension, despite suppression of plasma renin activity. Furthermore, in salt-loaded bilaterally renal denervated rats, Gαi(2) oligodeoxynucleotide infusion failed to evoke salt-sensitive hypertension. Therefore, in salt-resistant rats subjected to a chronic high-salt diet, brain Gαi(2) proteins are required to inhibit central sympathetic outflow to the kidneys and maintain sodium balance and normotension. In conclusion, these data demonstrate a central role of endogenous brain, likely paraventricular nucleus-specific, Gαi(2)-subunit protein-gated signal transduction pathways in maintaining a salt-resistant phenotype.

Indexed as

AnimalsBlood PressureBrainGTP-Binding Protein alpha Subunit, Gi2HomeostasisHypertensionKidneyMaleNeural PathwaysRatsRats, Sprague-DawleyReninSodium Chloride, DietarySympathectomySympathetic Nervous SystemGTP-Binding Protein alpha Subunit, Gi2ReninSodium Chloride, Dietary

Identifiers

PMID23213191
PMCPMC3562703
OpenAlexW2126724178

What OpenQuestion holds

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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.