Evidence map›Paper›PMID 37175592›Full record

ReviewInternational journal of molecular sciences2023

Molecular Mechanisms of Neurogenic Lower Urinary Tract Dysfunction after Spinal Cord Injury.

Nobutaka Shimizu, Tetsuichi Saito, Naoki Wada, Mamoru Hashimoto, Takahiro Shimizu, Joonbeom Kwon, Kang Jun Cho, Motoaki Saito, Sergei Karnup, William C de Groat and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
9.2field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Urogenital dysfunction in neurological diseases.Nature reviews. Neurology · 2026
    Review
  8. bioRxiv : the preprint server for biology · 2026
    Article
  9. Article
  10. Observational
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Serotonin (5-HT)CNS neuroscience & therapeutics · 2024
    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

11 authors at 2 institutions in 2 countries.

Nobutaka ShimizuDepartment of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.ORCID 0000-0003-4185-323X
Tetsuichi SaitoDepartment of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Naoki WadaDepartment of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.ORCID 0000-0002-9587-6798
Mamoru HashimotoDepartment of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.ORCID 0000-0002-4137-942X
Takahiro ShimizuDepartment of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Joonbeom KwonDepartment of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Kang Jun ChoDepartment of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.ORCID 0000-0002-5305-901X
Motoaki SaitoDepartment of Pharmacology, Kochi Medical School, Kochi University, Nankoku 783-8505, Japan.
Sergei KarnupDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA 15213, USA.
William C de GroatDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Naoki YoshimuraDepartment of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.ORCID 0000-0001-8070-1664
University of Pittsburgh · USKōchi University · JP

Funding

Intraspinal circuits supporting synergy between the bladder and urethral sphincter in miceR01DK129194 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KARNUP, SERGEI V, YOSHIMURA, NAOKI · 2021 to 2024
$1.4M
NIDDK NIH HHS R01 DK129194NIH HHS R01DK129194
6 · The paper itself

Abstract

This article provides a synopsis of current progress made in fundamental studies of lower urinary tract dysfunction (LUTD) after spinal cord injury (SCI) above the sacral level. Animal models of SCI allowed us to examine the effects of SCI on the micturition control and the underlying neurophysiological processes of SCI-induced LUTD. Urine storage and elimination are the two primary functions of the LUT, which are governed by complicated regulatory mechanisms in the central and peripheral nervous systems. These neural systems control the action of two functional units in the LUT: the urinary bladder and an outlet consisting of the bladder neck, urethral sphincters, and pelvic-floor striated muscles. During the storage phase, the outlet is closed, and the bladder is inactive to maintain a low intravenous pressure and continence. In contrast, during the voiding phase, the outlet relaxes, and the bladder contracts to facilitate adequate urine flow and bladder emptying. SCI disrupts the normal reflex circuits that regulate co-ordinated bladder and urethral sphincter function, leading to involuntary and inefficient voiding. Following SCI, a spinal micturition reflex pathway develops to induce an overactive bladder condition following the initial areflexic phase. In addition, without proper bladder-urethral-sphincter coordination after SCI, the bladder is not emptied as effectively as in the normal condition. Previous studies using animal models of SCI have shown that hyperexcitability of C-fiber bladder afferent pathways is a fundamental pathophysiological mechanism, inducing neurogenic LUTD, especially detrusor overactivity during the storage phase. SCI also induces neurogenic LUTD during the voiding phase, known as detrusor sphincter dyssynergia, likely due to hyperexcitability of Aδ-fiber bladder afferent pathways rather than C-fiber afferents. The molecular mechanisms underlying SCI-induced LUTD are multifactorial; previous studies have identified significant changes in the expression of various molecules in the peripheral organs and afferent nerves projecting to the spinal cord, including growth factors, ion channels, receptors and neurotransmitters. These findings in animal models of SCI and neurogenic LUTD should increase our understanding of pathophysiological mechanisms of LUTD after SCI for the future development of novel therapies for SCI patients with LUTD.

Indexed as

Spinal Cord InjuriesUrinary Bladder, OveractiveAnimalsSpinal CordUrinary BladderUrinationAδ-fiber afferentC-fiber afferentdetrusor overactivitydetrusor–sphincter dyssynergiafibrosisspinal-cord injury

Identifiers

PMID37175592
PMCPMC10177842
OpenAlexW4367183129

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.