Evidence map›Paper›PMID 32383030›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2020

Protective effect of oleuropein on ketamine-induced cardiotoxicity in rats.

Mehmet Selim Çömez, Mustafa Cellat, Hüseyin Özkan, Yakup Borazan, Tuba Aydın, İshak Gökçek, Erdinç Türk, Mehmet Güvenç, Ahmet Çakır, Şule Yurdagül Özsoy

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In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 22 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

10 authors at 5 institutions in 1 country.

Mehmet Selim ÇömezDepartment of Anesthesiology and Reanimation, Faculty of Medicine, Hatay Mustafa Kemal University, 31300, Hatay, Turkey. mehmetcomez@mku.edu.tr.ORCID 0000-0003-0821-5148
Mustafa CellatDepartment of Physiology, Faculty of Veterinary Medicine, Hatay Mustafa Kemal University, Hatay, Turkey.
Hüseyin ÖzkanDepartment of Genetics, Faculty of Veterinary Medicine, Hatay Mustafa Kemal University, Hatay, Turkey.
Yakup BorazanAdıyaman University, Education And Research Hospital, Adıyaman, Turkey.
Tuba AydınDepartment of Pharmacognosy, Faculty of Pharmacy, Ağrı İbrahim Çeçen University, Agrı, Turkey.
İshak GökçekDepartment of Physiology, Faculty of Veterinary Medicine, Hatay Mustafa Kemal University, Hatay, Turkey.
Erdinç TürkDepartment of Pharmacology and Toxicology, Faculty of Veterinary Medicine, Hatay Mustafa Kemal University, Hatay, Turkey.
Mehmet GüvençDepartment of Physiology, Faculty of Veterinary Medicine, Hatay Mustafa Kemal University, Hatay, Turkey.
Ahmet ÇakırDepartment of Chemistry, Faculty of Science and Letters, Kilis 7 Aralık University, Kilis, Turkey.
Şule Yurdagül ÖzsoyDepartment of Pathology, Faculty of Veterinary Medicine, Adnan Menderes University, Aydın, Turkey.
Mustafa Kemal University · TRAdıyaman University · TRAdnan Menderes University · TRAğrı İbrahim Çeçen University · TRKilis 7 Aralık University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The antioxidant and cardioprotective effects of oleuropein have been reported in several studies; however, its effect on ketamine cardiotoxicity has not been known yet. The aim of this study was to investigate the effects of oleuropein in ketamine-induced cardiotoxicity model in rats. A total of 28 male Wistar Albino rats were included in the study and they were randomly divided into four groups, each having seven rats. Group 1 (control): rats were given 1 mL of DMSO by oral gavage method for 7 days. Group 2 (ketamine): on the seventh day of the study, 60 mg/kg ketamine was administered intraperitoneally. Then, 60 mg/kg ketamine was administered intraperitoneally every 10 min for 3 h. Group 3 (oleuropein): rats were given 200 mg/kg/day oleuropein by oral gavage method for 7 days. Group 4 (oleuropein + ketamine): rats were given 1 × 200 mg/kg oleuropein by oral gavage method for 7 days. Furthermore, 60 mg/kg ketamine was administered intraperitoneally on the seventh day of the experiment. Then, 60 mg/kg ketamine was administered intraperitoneally every 10 min for 3 h. Serum cardiac marker (TnI, CK-MB and CK) levels were measured. Histopathological analysis was performed on a portion of the cardiac tissue. Cardiac tissue oxidative stress and antioxidant markers (MDA, GSH, GSH.Px and CAT), TNF-α, IL-6, NF-κB, COX-2 and Nrf-2 gene expressions, and protein conversion levels of related genes were determined. Data obtained showed that ketamine administration increased MDA (p < 0.001), TNF-α (p < 0.01), IL-6 (p < 0.01), COX-2 (p < 0.001) and NF-κB (p < 0.001) levels, as well as serum TnI (p < 0.001), CK-MB (p < 0.001) and CK (p < 0.01) levels whereas decreased GSH (p < 0.05) and Nrf-2 (p < 0.05) levels, as well as GSH-Px (p < 0.001) and CAT (p < 0.05) enzyme activities. Oleuropein administration was observed to decrease MDA, TNF-α, IL-6, COX-2, NF-κB, TnI, CK-MB and CK levels close to the control group and to increase GSH levels and GSH-Px and CAT enzyme activities close to the control group. This study showed that oleuropein administration reversed the increased oxidative stress and inflammation as a result of the use of ketamine and had protective effects on the heart.

Indexed as

AnimalsAnti-Inflammatory AgentsAntioxidantsCardiotoxicityDisease Models, AnimalHeart DiseasesInflammation MediatorsIridoid GlucosidesKetamineMaleMyocytes, CardiacOxidative StressRats, WistarSignal TransductionAnti-Inflammatory AgentsAntioxidantsInflammation MediatorsIridoid GlucosidesKetamineoleuropeinCardiotoxicityKetamineOleuropein

Identifiers

PMID32383030
OpenAlexW3023016359

What OpenQuestion holds

Textmetadata
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.