Evidence map›Paper›PMID 22933301›Full record

ArticleAmerican journal of physiology. Renal physiology2012

Use of ultrasound to assess renal reperfusion and P-selectin expression following unilateral renal ischemia.

Erika I Boesen, G Ryan Crislip, Jennifer C Sullivan

Open access · greenAbstract readComparative StudyEvaluation Study
In one paragraph

Article in American journal of physiology. Renal physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Non-invasive molecular imaging of kidney diseases.Nature reviews. Nephrology · 2021
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. ETPhysiological reports · 2018
    Article
  10. Review
  11. Long-Term Administration of Angiotensin (1-7) toOxidative medicine and cellular longevity · 2018
    Article
  12. New Ultrasound Techniques Promise Further Advances in AKI and CKD.Journal of the American Society of Nephrology : JASN · 2017
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Taking a sound approach to acute kidney injury.American journal of physiology. Renal physiology · 2012
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Erika I BoesenSection of Experimental Medicine, Department of Medicine, Georgia Health Sciences University, Augusta, GA 30912, USA.
G Ryan Crislip
Jennifer C Sullivan
Augusta University Health · US

Funding

Sexual dimorphisms of renin-angiotensin system in hypertension and renal injuryR01HL093271 · NHLBI · AUGUSTA UNIVERSITY · PI SULLIVAN, JENNIFER C · 2009 to 2013
$1.8M
NHLBI NIH HHS HL-093271
6 · The paper itself

Abstract

Renal ischemia-reperfusion injury is a major cause of acute kidney injury that carries a high mortality rate and increases the risk of later development of hypertension and chronic kidney disease. Although mouse models have contributed much to our understanding of the mechanisms involved, studying aspects of the injury process in vivo remains technically challenging. This study validates the use of noninvasive ultrasound imaging to assess both renal perfusion and vascular adhesion molecule expression following 1-h unilateral renal ischemia in male and female mice. Pulsed-wave Doppler measurements of renal arterial blood velocity revealed renal perfusion recoveries of 56 ± 9% in male and 69 ± 10% in female mice 1 h after the commencing of reperfusion, which is similar to what we have previously published using conventional invasive methodology. At 24 h postischemia, renal perfusion was 40 ± 8% in male and 46 ± 7% in female mice, representing a further significant reduction of perfusion (P(Time) < 0.001). Using ultrasound imaging of a P-selectin-targeted contrast agent, a significant increase in vascular P-selectin protein expression was observed after 1-h reperfusion in the cortex of the postischemic compared with contralateral kidney in both male and female mice (18 ± 5 vs. 3 ± 3 intensity units in male and 30 ± 6 vs. 0 ± 4 in female mice, P(Ischemia) < 0.01). An approximately sixfold increase in P-selectin mRNA was observed ex vivo in the renal vasculature of male and female mice at this time point (P < 0.01). In conclusion, ultrasound represents an effective and noninvasive method for the measurement of both renal perfusion and vascular adhesion molecule expression in mice.

Indexed as

AnimalsBlood Flow VelocityCell Adhesion MoleculesDisease Models, AnimalFemaleKidneyMaleMiceMice, Inbred C57BLP-SelectinRegional Blood FlowRenal ArteryReperfusion InjurySex CharacteristicsTime FactorsUltrasonography, Doppler, PulsedCell Adhesion MoleculesP-Selectin

Identifiers

PMID22933301
PMCPMC3518191
OpenAlexW2152723823

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.