Evidence map›Paper›PMID 33009887›Full record

ArticleJournal of cellular and molecular medicine2020

Changes in the expression and function of the PDE5 pathway in the obstructed urinary bladder.

Weixiang He, Han Xiang, Daoquan Liu, Jianmin Liu, Mingzhou Li, Qian Wang, Qiaofeng Qian, Yan Li, Xun Fu, Ping Chen and 7 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-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

5 citing papers in PubMed, 11 citations in OpenAlex.

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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

17 authors at 3 institutions in 2 countries.

Weixiang HeDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.ORCID 0000-0002-4366-8321
Han XiangDepartment of Urology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Daoquan LiuDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Jianmin LiuDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Mingzhou LiDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Qian WangDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Qiaofeng QianDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Yan LiDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Xun FuDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Ping ChenDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Yuming GuoDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Guang ZengDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Zhonghua WuDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Daxing ZhanDepartment of Anesthesiology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Xinghuan WangDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Michael E DiSantoDepartment of Surgery and Biomedical Sciences, Cooper Medical School of Rowan University, Camden, NJ, USA.
Xinhua ZhangDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.ORCID 0000-0003-0267-428X
Wuhan University · CNCooper Medical School of Rowan University · USSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our study aims to explore changes in bladder contractility and the phosphodiesterase type 5 (PDE5) signalling pathway in response to partial bladder outlet obstruction (PBOO). A surgically induced male rat PBOO model and human obstructed bladder tissues were used. Histological changes were examined by H&E and Masson's trichrome staining. Bladder strip contractility was measured via organ bath. The expressions of nitric oxide synthase (NOS) isoforms, PDE5, muscarinic cholinergic receptor (CHRM) isoforms and PDE4 isoforms in bladder were detected by RT-PCR and Western blotting. The immunolocalization of the PDE5 protein and its functional activity were also determined. PBOO bladder tissue exhibited significant SM hypertrophy and elevated responsiveness to KCl depolarization and the muscarinic receptor agonist carbachol. NOS isoforms, PDE5, CHRM2, CHRM3 and PDE4A were up-regulated in obstructed bladder tissue, whereas no change in PDE4B and PDE4D isoform expression was observed. With regard to PDE5, it was expressed in the SM bundles of bladder. Interestingly, obstructed bladder exhibited less relaxation responsiveness to sodium nitroprusside (SNP), but an exaggerated PDE5 inhibition effect. The up-regulation of PDE5 could contribute to the lack of effect on Q

Indexed as

Gene Expression ProfilingAnimalsBody WeightCyclic Nucleotide Phosphodiesterases, Type 5HumansMaleMuscle ContractionMuscle, SmoothNitroprussideOrgan SizeProstatic HyperplasiaProtein IsoformsRatsRats, Sprague-DawleyReceptors, MuscarinicUrinary BladderCyclic Nucleotide Phosphodiesterases, Type 5NitroprussidePDE5A protein, humanPde5a protein, ratProtein IsoformsReceptors, Muscarinicbenign prostate hyperplasialower urinary tract symptomspartial bladder outlet obstructionphosphodiesterase type 5

Identifiers

PMID33009887
PMCPMC7701571
OpenAlexW3089988972

What OpenQuestion holds

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LicenceCC BY
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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.