Evidence map›Paper›PMID 31660030›Full record

ArticleWorld journal of gastroenterology2019

STW 5 is effective against nonsteroidal anti-inflammatory drugs induced gastro-duodenal lesions in rats.

Mohamed T Khayyal, Walaa Wadie, Enas A Abd El-Haleim, Kawkab A Ahmed, Olaf Kelber, Ramy M Ammar, Heba Abdel-Aziz

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2019. 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
0.7field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. An integrated network analysis, RNA-seq andFrontiers in pharmacology · 2023
    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

7 authors at 1 institution in 1 country.

Mohamed T KhayyalDepartment of Pharmacology, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt. mtkhayyal@gmail.com.
Walaa WadieDepartment of Pharmacology, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt.
Enas A Abd El-HaleimDepartment of Pharmacology, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt.
Kawkab A AhmedDepartment of Pathology, Faculty of Veterinary Medicine, Cairo University, Cairo 12211, Egypt.
Olaf KelberSteigerwald Arzneimittelwerk GmbH, Bayer Consumer Health, Darmstadt 64295, Germany.
Ramy M AmmarSteigerwald Arzneimittelwerk GmbH, Bayer Consumer Health, Darmstadt 64295, Germany.
Heba Abdel-AzizSteigerwald Arzneimittelwerk GmbH, Bayer Consumer Health, Darmstadt 64295, Germany.
Cairo University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProton pump inhibitors are often used to prevent gastro-intestinal lesions induced by nonsteroidal anti-inflammatory drugs. However, they are not always effective against both gastric and duodenal lesions and their use is not devoid of side effects.

aimTo explore the mechanisms mediating the clinical efficacy of STW 5 in gastro-duodenal lesions induced by nonsteroidal anti-inflammatory drugs (NSAIDs), exemplified here by diclofenac, in a comparison to omeprazole.

methodsGastro-duodenal lesions were induced in rats by oral administration of diclofenac (5 mg/kg) for 6 successive days. One group was given concurrently STW 5 (5 mL/kg) while another was given omeprazole (20 mg/kg). A day later, animals were sacrificed, stomach and duodenum excised and divided into 2 segments: One for histological examination and one for measuring inflammatory mediators (tumor necrosis factor α, interleukins-1β and 10), oxidative stress enzyme (heme oxygenase-1) and apoptosis regulator (B-cell lymphoma 2).

resultsDiclofenac caused overt histological damage in both tissues, associated with parallel changes in all parameters measured. STW 5 and omeprazole effectively prevented these changes, but STW 5 superseded omeprazole in protecting against histological damage, particularly in the duodenum.

conclusionThe findings support the therapeutic usefulness of STW 5 and its superiority over omeprazole as adjuvant therapy to NSAIDs to protect against their possible gastro-duodenal side effects.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalDiclofenacDisease Models, AnimalDuodenal UlcerDuodenumFemaleGastric MucosaHumansIntestinal MucosaPlant ExtractsProtective AgentsRatsRats, WistarStomach UlcerTreatment OutcomeAnti-Inflammatory Agents, Non-SteroidalDiclofenaciberogastPlant ExtractsProtective AgentsDiclofenacGastro-intestinal lesionsInflammationOmeprazoleSTW 5

Identifiers

PMID31660030
PMCPMC6815791
OpenAlexW2980576782

What OpenQuestion holds

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LicenceCC BY-NC
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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.