Evidence map›Paper›PMID 35655356›Full record

ArticleTransplantation2022

The Selective Estrogen Receptor Modulator, Raloxifene, Is Protective Against Renal Ischemia-reperfusion Injury.

Paul Hernandez, Ciaran O'Brien, Seth J Concors, Zhonglin Wang, Guanghui Ge, Wayne W Hancock, Matthew H Levine

Abstract read
In one paragraph

Article in Transplantation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
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  6. Article
  7. Sex as a biological variable: Mechanistic insights and clinical relevance in solid organ transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2023
    Review
  8. Article
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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

7 authors at 2 institutions in 1 country.

Paul HernandezDepartment of Surgery, University of Pennsylvania, Philadelphia, PA.
Ciaran O'BrienDepartment of Surgery, University of Pennsylvania, Philadelphia, PA.
Seth J ConcorsDepartment of Surgery, University of Pennsylvania, Philadelphia, PA.
Zhonglin WangDepartment of Surgery, University of Pennsylvania, Philadelphia, PA.
Guanghui GeDepartment of Surgery, University of Pennsylvania, Philadelphia, PA.
Wayne W HancockDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA.
Matthew H LevineDepartment of Surgery, University of Pennsylvania, Philadelphia, PA.
University of Pennsylvania · USChildren's Hospital of Philadelphia · US

Funding

Estrogen and Serms as Therapy for Renal Ischemia Reperfusion InjuryR01DK139679 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Wayne William Hancock, Matthew Howard Levine · 2024 to 2026
$2.8M
HDAC2 Inhibition Mitigates Renal Ischemia Reperfusion InjuryR01DK106243 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI LEVINE, MATTHEW HOWARD · 2016 to 2020
$1.8M
NIDDK NIH HHS R01 DK106243NIDDK NIH HHS R01 DK139679
6 · The paper itself

Abstract

backgroundThere is increasing evidence that estrogen is responsible for improved outcomes in female kidney transplant recipients. Although the exact mechanism is not yet known, estrogen appears to exert its protective effects by ameliorating ischemia-reperfusion injury (IRI). In this study, we have examined whether the beneficial effects of exogenous estrogen in renal IRI are replicated by therapy with any one of several selective estrogen receptor modulators.

methodsC57BL/6 adult mice underwent standardized warm renal ischemia for 28 min after being injected with the selective estrogen receptor modulators, raloxifene, lasofoxifene, tamoxifen, bazedoxifene, or control vehicle (dimethyl sulfoxide), at 16 and 1 h before IRI. Plasma concentrations of blood urea nitrogen and creatinine were assessed 24, 48, 72, and 96 h post-IRI. Tissue was collected 30 d postischemia for fibrosis analysis using Sirius Red staining.

resultsRaloxifene treatment in female mice resulted in significantly lower blood urea nitrogen and creatinine after IRI and significantly lower fibrosis 30 d following IRI.

conclusionsRaloxifene is protective against both acute kidney injury and fibrosis resulting from renal IRI in a mouse model.

Indexed as

Acute Kidney InjuryReperfusion InjuryAnimalsCreatinineDimethyl SulfoxideEstrogensFemaleFibrosisKidneyMiceMice, Inbred C57BLRaloxifene HydrochlorideSelective Estrogen Receptor ModulatorsCreatinineDimethyl SulfoxideEstrogensRaloxifene HydrochlorideSelective Estrogen Receptor Modulators

Identifiers

PMID35655356
PMCPMC12063156
OpenAlexW4281694585

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.