Evidence map›Paper›PMID 39292699›Full record

ArticlePloS one2024

PDE5 inhibitor potentially improves polyuria and bladder storage and voiding dysfunctions in type 2 diabetic rats.

Takafumi Kabuto, So Inamura, Hisato Kobayashi, Xinmin Zha, Keiko Nagase, Minekatsu Taga, Masaya Seki, Nobuki Tanaka, Yoshinaga Okumura, Osamu Yokoyama and 1 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

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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

2 citing papers in PubMed.

  1. Review
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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

11 authors.

Takafumi KabutoDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.
So InamuraDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.
Hisato KobayashiDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.
Xinmin ZhaDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.
Keiko NagaseDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.
Minekatsu TagaDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.
Masaya SekiDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.
Nobuki TanakaDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.
Yoshinaga OkumuraDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.
Osamu YokoyamaDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.
Naoki TeradaDepartment of Urology, Faculty of Medical Science, University of Fukui, Fukui, Japan.ORCID 0009-0005-1082-6089

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBladder dysfunction associated with type 2 diabetes mellitus (T2DM) includes urine storage and voiding disorders. We examined pathological conditions of the bladder wall in a rat T2DM model and evaluated the effects of the phosphodiesterase-5 (PDE-5) inhibitor tadalafil. MATERIALS AND

methodsMale Otsuka Long-Evans Tokushima Fatty (OLETF) rats and Long-Evans Tokushima Otsuka (LETO) rats were used as the T2DM and control groups, respectively. Tadalafil was orally administered for 12 weeks. Micturition behavior was monitored using metabolic cages, and bladder function was evaluated by cystometry. Bladder blood flow was evaluated by laser speckle imaging, and an organ bath bladder distention test was used to measure adenosine triphosphate (ATP) release from the bladder urothelium. The expression levels of vesicular nucleotide transporter (VNUT), hypoxia markers, pro-inflammatory cytokines and growth factors in the bladder wall were measured using real-time polymerase chain reaction and enzyme-linked immunosorbent assay. Bladder wall contractions in response to KCl and carbachol were monitored using bladder-strip tests.

resultsWith aging, OLETF rats had higher micturition frequency and greater urine volume than LETO rats. Although bladder capacity was not significantly different, non-voiding bladder contraction occurred more frequently in OLETF rats than in LETO rats. Bladder blood flow was decreased and ATP release was increased with higher VNUT expression in OLETF rats than in LETO rats. These effects were suppressed by tadalafil administration, with accompanying decreased HIF-1α, 8-OHdG, IL-6, TNF-α, IGF-1, and bFGF expression. The impaired contractile responses of bladder strips to KCl and carbachol in OLETF rats with aging were restored by tadalafil administration.

conclusionsThe T2DM rats had polyuria, increased ATP release induced by decreased bladder blood flow and impaired contractile function. PDE5 inhibition improved these changes and may prevent T2DM-associated urinary frequency and bladder storage and voiding dysfunctions.

Indexed as

Diabetes Mellitus, Type 2Phosphodiesterase 5 InhibitorsPolyuriaTadalafilUrinary BladderAdenosine TriphosphateAnimalsDiabetes Mellitus, ExperimentalMaleMuscle ContractionRatsRats, Inbred OLETFUrinationAdenosine TriphosphatePhosphodiesterase 5 InhibitorsTadalafil

Identifiers

PMID39292699
PMCPMC11410213

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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.