Evidence map›Paper›PMID 21325646›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2011

Neuronostatin acts in brain to biphasically increase mean arterial pressure through sympatho-activation followed by vasopressin secretion: the role of melanocortin receptors.

Gina L C Yosten, Alicia T Pate, Willis K Samson

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Expression and function of nesfatin-1 are altered by stage of the estrous cycle.American journal of physiology. Regulatory, integrative and comparative physiology · 2019
    Article
  4. Review
  5. Novel regulator of vasopressin secretion: phoenixin.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    Article
  6. Article
  7. Review
  8. Association between a polymorphic poly-T repeat sequence in the promoter of the somatostatin gene and hypertension.Hypertension research : official journal of the Japanese Society of Hypertension · 2016
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Role of leptin and central nervous system melanocortins in obesity hypertension.Current opinion in nephrology and hypertension · 2013
    Review
  14. Evidence for an interaction of neuronostatin with the orphan G protein-coupled receptor, GPR107.American journal of physiology. Regulatory, integrative and comparative physiology · 2012
    Article
  15. Article
  16. 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

3 authors at 1 institution in 1 country.

Gina L C YostenDept. of Pharmacological and Physiological Science, Saint Louis University, St Louis, MO 63104, USA. gyosten@slu.edu
Alicia T Pate
Willis K Samson
Saint Louis University · US

Funding

Pharmacological Sciences Training GrantT32GM008306 · NIGMS · SAINT LOUIS UNIVERSITY · PI EGAN, TERRANCE M, WALKER, JOHN K. · 1990 to 2020
$3.6M
PHYSIOLOGY OF THE PROLACTIN RELEASING PEPTIDESR01HL066023 · NHLBI · SAINT LOUIS UNIVERSITY · PI SAMSON, WILLIS K. · 2001 to 2010
$2.0M
NHLBI NIH HHS HL-66023NHLBI NIH HHS R01 HL066023NIGMS NIH HHS 5T32GM008306
6 · The paper itself

Abstract

Neuronostatin is a recently described neuropeptide that is derived from the somatostatin preprohormone. We have shown previously that neuronostatin led to a biphasic, dose-related increase in mean arterial pressure when injected into the lateral cerebroventricle of adult, male rats. Because neuronostatin depolarized both magnocellular and parvocellular, paraventricular nucleus neurons in hypothalamic slice preparations, we hypothesized that neuronostatin elevated mean arterial pressure first by stimulating sympathetic nervous system activity followed by the release of a pressor hormone, specifically vasopressin. We found that the first phase of neuronostatin-induced increase in mean arterial pressure was reversed by pretreatment with phentolamine, indicating that phase 1 was, indeed, due to an increase in sympathetic activity. We also found that centrally injected neuronostatin led to a dose-related increase in vasopressin secretion in a time course consistent with the peak of the second phase. Furthermore, the second phase of arterial pressure elevation was reversed by pretreatment with a vasopressin 1 receptor antagonist, indicating that phase 2 was likely due to an increase in vasopressin secretion. We previously have shown that the anorexigenic and antidipsogenic effects of neuronostatin were reversed by pretreatment with the melanocortin 3/4 receptor antagonist, SHU9119, so we evaluated the ability of SHU9119 to reverse the effects of neuronostatin on MAP and vasopressin secretion. We found that SHU9119 abrogated the second phase of neuronostatin-induced increase in MAP and neuronostatin-induced vasopressin secretion, indicating that neuronostatin acts through the central melanocortin system to increase vasopressin release, ultimately leading to an elevation in MAP.

Indexed as

Adrenergic alpha-AntagonistsAnimalsBlood PressureBrainDose-Response Relationship, DrugHormone AntagonistsInjections, IntraventricularMaleMelanocyte-Stimulating HormonesPeptide FragmentsPhentolamineRatsReceptors, MelanocortinReceptors, VasopressinSomatostatinSympathetic Nervous SystemAdrenergic alpha-AntagonistsHormone AntagonistsMelanocyte-Stimulating HormonesPeptide FragmentsPhentolamineReceptors, MelanocortinReceptors, VasopressinSHU 9119SomatostatinVasopressins

Identifiers

PMID21325646
PMCPMC3094032
OpenAlexW2064784255

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.