Evidence map›Paper›PMID 27450022›Full record

ArticleThe Kaohsiung journal of medical sciences2016

The effects of tadalafil and pentoxifylline on apoptosis and nitric oxide synthase in liver ischemia/reperfusion injury.

Sibel Bektas, Kemal Karakaya, Murat Can, Burak Bahadir, Berrak Guven, Nilsen Erdogan, Sukru Oguz Ozdamar

Open access · goldAbstract read
In one paragraph

Article in The Kaohsiung journal of medical sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  6. Review
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  11. Review
  12. Chronic liver diseases and erectile dysfunction.Frontiers in public health · 2022
    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

7 authors at 2 institutions in 1 country.

Sibel BektasDepartment of Pathology, Gaziosmanpasa Taksim Training and Research Hospital, Gaziosmanpasa, Istanbul, Turkey. Electronic address: sibel_bektas@yahoo.com.
Kemal KarakayaDepartment of General Surgery, Bulent Ecevit University, School of Medicine, Kozlu, Zonguldak, Turkey.
Murat CanDepartment of Biochemistry, Bulent Ecevit University, School of Medicine, Kozlu, Zonguldak, Turkey.
Burak BahadirDepartment of Pathology, Bulent Ecevit University, School of Medicine, Kozlu, Zonguldak, Turkey.
Berrak GuvenDepartment of Biochemistry, Bulent Ecevit University, School of Medicine, Kozlu, Zonguldak, Turkey.
Nilsen ErdoganDepartment of Pathology, Gaziosmanpasa Taksim Training and Research Hospital, Gaziosmanpasa, Istanbul, Turkey.
Sukru Oguz OzdamarDepartment of Pathology, Bulent Ecevit University, School of Medicine, Kozlu, Zonguldak, Turkey.
Bülent Ecevit University · TRGaziosmanpaşa Taksim Eğitim ve Araştırma Hastanesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate the effects of tadalafil (TDF) and pentoxifylline (PTX) on hepatic apoptosis and the expressions of endothelial and inducible nitric oxide synthases (eNOS and iNOS) after liver ischemia/reperfusion (IR). Forty Wistar albino rats were randomly divided into five groups (n=8) as follows: sham group; IR group with ischemia/reperfusion alone; low-dose and high-dose TDF groups received 2.5 mg/kg and 10 mg/kg TDF, respectively; and PTX group received 40 mg/kg PTX. Blood was collected for the analysis of serum alanine aminotransferase, aspartate aminotransferase, γ-glutamyl transferase, uric acid, malondialdehyde (MDA), and total antioxidant capacity (TAC). MDA and TAC also were measured in liver tissue. Histopathological examination was performed to assess the severity of hepatic injury. Apoptosis was evaluated using the apoptosis protease-activating factor 1 (APAF-1) antibody; the expressions of eNOS and iNOS were also assessed by immunohistochemistry in all groups. Serum alanine aminotransferase, aspartate aminotransferase, γ-glutamyl transferase, uric acid, MDA, and TAC, tissue MDA and TAC levels, hepatic injury, and score for extent and for intensity of eNOS, iNOS, and apoptosis protease-activating factor 1 were significantly different in TDF and PTX groups compared to the IR group. High dose-TDF and PTX have the best protective effect on IR-induced liver tissue damage. This study showed that TDF and PTX supplementation may be helpful in preventing free oxygen radical damage, lipid peroxidation, hepatocyte necrosis, and apoptosis in liver IR injury and minimizing liver damage.

Indexed as

AnimalsApoptosisApoptotic Protease-Activating Factor 1FemaleImmunohistochemistryLiverNitric Oxide SynthasePentoxifyllineRats, WistarReperfusion InjuryTadalafilApoptotic Protease-Activating Factor 1Nitric Oxide SynthasePentoxifyllineTadalafilIschemia/reperfusionLiverPentoxifyllineTadalafil

Identifiers

PMID27450022
PMCPMC11916170
OpenAlexW2414266139

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.