Evidence map›Paper›PMID 30282823›Full record

ArticleJCI insight2018

Arginine vasopressin infusion is sufficient to model clinical features of preeclampsia in mice.

Jeremy A Sandgren, Guorui Deng, Danny W Linggonegoro, Sabrina M Scroggins, Katherine J Perschbacher, Anand R Nair, Taryn E Nishimura, Shao Yang Zhang, Larry N Agbor, Jing Wu and 14 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
6.3field-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

47 citing papers in PubMed, 2 syntheses or guidelines pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Guidelines for assessing maternal cardiovascular physiology during pregnancy and postpartum.American journal of physiology. Heart and circulatory physiology · 2024
    Guideline
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Cardiovascular complications of pregnancy.The Journal of clinical investigation · 2026
    Review
  9. Review
  10. Localization and quantification of placentalPhysiological genomics · 2025
    Article
  11. Article
  12. Article
  13. Review
  14. Role of vasopressin for chronic hypertension in pregnancy.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Article
  15. Anti-angiogenic mechanisms and serotonergic dysfunction in the Rgs2 knockout model for the study of psycho-obstetric risk.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  16. Article
  17. Article
  18. Article
  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

24 authors at 3 institutions in 3 countries.

Jeremy A SandgrenDepartment of Pharmacology.
Guorui DengDepartment of Pharmacology.
Danny W LinggonegoroDepartment of Pharmacology.
Sabrina M ScrogginsDepartment of Obstetrics & Gynecology.
Katherine J PerschbacherDepartment of Pharmacology.
Anand R NairDepartment of Pharmacology.
Taryn E NishimuraDepartment of Obstetrics & Gynecology.
Shao Yang ZhangDepartment of Pharmacology.
Larry N AgborDepartment of Pharmacology.
Jing WuDepartment of Pharmacology.
Henry L KeenDepartment of Pharmacology.
Meghan C NaberDepartment of Pharmacology.
Nicole A PearsonDepartment of Pharmacology.
Kathy A ZimmermanDepartment of Internal Medicine.
Robert M WeissDepartment of Internal Medicine.
Noelle C BowdlerDepartment of Obstetrics & Gynecology.
Yuriy M UsachevDepartment of Pharmacology.
Donna A SantillanDepartment of Obstetrics & Gynecology.
Matthew J PotthoffDepartment of Pharmacology.
Gary L PierceDepartment of Health & Human Physiology.
Katherine N Gibson-CorleyDepartment of Pathology.
Curt D SigmundDepartment of Pharmacology.
Mark K SantillanDepartment of Obstetrics & Gynecology.
Justin L GrobeDepartment of Pharmacology.
University of Iowa · USUniversity of Iowa Hospitals and Clinics · USFraternal Order of Eagles · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
Role of the brain Renin-Angiotensin Sys. in Cardiovas and Metabolic RegulationP01HL084207 · NHLBI · UNIVERSITY OF IOWA · PI GROBE, JUSTIN L · 2007 to 2022
$30.2M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007337 · NIGMS · UNIVERSITY OF IOWA · PI GEYER, PAMELA K., LENTZ, STEVEN R · 1985 to 2020
$15.9M
INTERDISCIPLINARY IMMUNOLOGY TRAINING PROGRAMT32AI007260 · NIAID · UNIVERSITY OF IOWA · PI BUTLER, NOAH SULLIVAN, WU, LI · 1986 to 2023
$5.7M
Interaction between leptin and angiotensin in the pathogenesis of obesity-hypertensionR01HL134850 · NHLBI · UNIVERSITY OF IOWA · PI Justin L Grobe · 2017 to 2026
$4.4M
Predoctoral Training in the Pharmacological SciencesT32GM067795 · NIGMS · UNIVERSITY OF IOWA · PI STRACK, STEFAN · 2004 to 2021
$3.4M
Mitochondria fission and fusion (MFF)-dependent mechanisms in neuronal toxicityR01NS087068 · NINDS · UNIVERSITY OF IOWA · PI USACHEV, YURIY M · 2014 to 2017
$1.3M
High-Resolution Research UltrasoundS10OD019941 · OD · UNIVERSITY OF IOWA · PI WEISS, ROBERT M · 2015 to 2015
$298k
NCI NIH HHS P30 CA086862NHLBI NIH HHS P01 HL084207NHLBI NIH HHS R01 HL134850NIAID NIH HHS T32 AI007260NIGMS NIH HHS T32 GM007337NIGMS NIH HHS T32 GM067795NIH HHS S10 OD019941NINDS NIH HHS R01 NS087068
6 · The paper itself

Abstract

Copeptin, a marker of arginine vasopressin (AVP) secretion, is elevated throughout human pregnancies complicated by preeclampsia (PE), and AVP infusion throughout gestation is sufficient to induce the major phenotypes of PE in mice. Thus, we hypothesized a role for AVP in the pathogenesis of PE. AVP infusion into pregnant C57BL/6J mice resulted in hypertension, renal glomerular endotheliosis, intrauterine growth restriction, decreased placental growth factor (PGF), altered placental morphology, placental oxidative stress, and placental gene expression consistent with human PE. Interestingly, these changes occurred despite a lack of placental hypoxia or elevations in placental fms-like tyrosine kinase-1 (FLT1). Coinfusion of AVP receptor antagonists and time-restricted infusion of AVP uncovered a mid-gestational role for the AVPR1A receptor in the observed renal pathologies, versus mid- and late-gestational roles for the AVPR2 receptor in the blood pressure and fetal phenotypes. These findings demonstrate that AVP is sufficient to initiate phenotypes of PE in the absence of placental hypoxia, and indicate that AVP may mechanistically (independently, and possibly synergistically with hypoxia) contribute to the development of clinical signs of PE in specific subtypes of human PE. Additionally, they identify divergent and gestational time-specific signaling mechanisms that mediate the development of PE phenotypes in response to AVP.

Indexed as

AnimalsAntidiuretic Hormone Receptor AntagonistsBlood PressureBlood Pressure DeterminationCell HypoxiaDisease Models, AnimalFemaleHumansMiceMice, Inbred C57BLNeurophysinsPlacentaPlethysmographyPre-EclampsiaPregnancyProtein PrecursorsAntidiuretic Hormone Receptor AntagonistsAVP protein, humanAVPR1a receptor, mouseNeurophysinsProtein PrecursorsReceptors, VasopressinRecombinant ProteinsVasopressinsHypertensionMouse modelsObstetrics/gynecologyReproductive Biology

Identifiers

PMID30282823
PMCPMC6237463
OpenAlexW2895504925

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.