Evidence map›Paper›PMID 32696129›Full record

ArticleWorld journal of urology2021

The effect of botulinum toxin on ureteral inflammation.

Kevin Krughoff, Faith L Anderson, Scott Palisoul, Alison L Young, Jason R Pettus, Karen L Moodie, Christopher Ogomo, Steven S Tau, Rachel A Moses, Matthew C Havrda and 1 more

Abstract read
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In one paragraph

Article in World journal of urology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 2 institutions in 1 country.

Kevin KrughoffDepartment of Urology, Dartmouth-Hitchcock, 1 Medical Center Dr, Lebanon, NH, USA. Kevin.j.krughoff@hitchcock.org.ORCID http://orcid.org/0000-0002-7957-831X
Faith L AndersonDepartment of Molecular and Systems Biology, Geisel School of Medicine At Dartmouth and Dartmouth-Hitchcock Medical Center, 1 Medical Center Dr, Lebanon, NH, USA.
Scott PalisoulDepartment of Pathology, Dartmouth-Hitchcock, 1 Medical Center Dr, Lebanon, NH, USA.
Alison L YoungDepartment of Molecular and Systems Biology, Geisel School of Medicine At Dartmouth and Dartmouth-Hitchcock Medical Center, 1 Medical Center Dr, Lebanon, NH, USA.
Jason R PettusDepartment of Pathology, Dartmouth-Hitchcock, 1 Medical Center Dr, Lebanon, NH, USA.
Karen L MoodieCenter for Comparative Medicine and Research, Dartmouth College, Hanover, NH, USA.
Christopher OgomoElectron Microscopy, Dartmouth College, 5 Allen St, Hanover, NH, USA.
Steven S TauDepartment of Molecular and Systems Biology, Geisel School of Medicine At Dartmouth and Dartmouth-Hitchcock Medical Center, 1 Medical Center Dr, Lebanon, NH, USA.
Rachel A MosesDepartment of Urology, Dartmouth-Hitchcock, 1 Medical Center Dr, Lebanon, NH, USA.
Matthew C HavrdaDepartment of Molecular and Systems Biology, Geisel School of Medicine At Dartmouth and Dartmouth-Hitchcock Medical Center, 1 Medical Center Dr, Lebanon, NH, USA.
David R ChavezDepartment of Urology, Dartmouth-Hitchcock, 1 Medical Center Dr, Lebanon, NH, USA.
Dartmouth–Hitchcock Medical Center · USDartmouth College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe impact of onabotulinum toxin type A (BoNT-A) on bladder afferent nerve pathways and chemosensory functions is an active area of investigation. There may be a role for BoNT-A in disorders of the ureter; however, no histologic studies have assessed the effects of BoNT-A on ureteral tissue. Our objective was to develop an animal model of ureteral inflammation and determine the impact of ureteral BoNT-A instillation on known mechanisms of inflammation.

methodsThe safety and feasibility of a novel animal model of ureteral inflammation was assessed. Through open cystotomy, the effect of ureteral BoNT-A instillation on inflammation was determined through H&E, masson's trichrome, Ki-67 stain, and prostaglandin E (PGE) synthase expression, a known marker of pain and inflammation in ureteral tissue. Urothelial microstructure was assessed using electron microscopy and standard histologic techniques.

resultsAll experiments were carried to completion, and no systemic signs of botulinum toxicity were seen. BoNT-A exposure was associated with a decrease in PGE synthase expression in a dose-dependent fashion. BoNT-A exposure was not found to impact collagen deposition or cell proliferation. Disruption of tight junctions between urothelial cells was observed under conditions of inflammation.

conclusionWe describe the feasibility of a novel in vivo model of ureteral inflammation and report the first histologic study of the effects of BoNT-A on the ureter. Preliminary findings show that BoNT-A attenuates ureteral PGE synthase expression under conditions of inflammation. The application of BoNT-A may provide anti-inflammatory and analgesic effects in the context of ureteral disorders.

Indexed as

Acetylcholine Release InhibitorsAnimalsBotulinum Toxins, Type ADisease Models, AnimalFeasibility StudiesFemaleInflammationMaleRabbitsUreteral DiseasesAcetylcholine Release InhibitorsBotulinum Toxins, Type AincobotulinumtoxinABotulinum toxinHistologyInflammationProstaglandinUreter

Identifiers

PMID32696129
OpenAlexW3043985955

What OpenQuestion holds

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Registered trials

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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.