Evidence map›Paper›PMID 39200118›Full record

ArticleBiomedicines2024

Investigation of the Protective Effects of Magnesium on Bupivacaine-Induced Toxicity at the Level of Colon Cell Culture.

Ceren Önal, Kemal Tolga Saraçoğlu, Ayten Saraçoğlu, Beyza Nur Özkan, Eray Metin Güler, Gülten Arslan, Seçil Azime Karakuş, Yekbun Bulun, Tomasz Gaszynski, Pawel Ratajczyk

Abstract read
In one paragraph

Article in Biomedicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ceren ÖnalDepartment of Anesthesiology and Reanimation, Ağrı Research and Training Hospital, Ağrı 04200, Türkiye.
Kemal Tolga SaraçoğluDepartment of Anaesthesiology, ICU & Perioperative Medicine, Hazm Mebaireek General Hospital HMC, Qatar University College of Medicine, Doha P.O. Box 2713, Qatar.
Ayten SaraçoğluDepartment of Anaesthesiology, ICU & Perioperative Medicine, Aisha Bint Hamad Al Attiyah Hospital HMC, Qatar University College of Medicine, Doha P.O. Box 2713, Qatar.ORCID 0000-0002-1186-0933
Beyza Nur ÖzkanDepartment of Medical Biochemistry, Hamidiye Faculty of Medicine, University of Health Sciences Türkiye, İstanbul 34480, Türkiye.
Eray Metin GülerDepartment of Medical Biochemistry, Hamidiye Faculty of Medicine, University of Health Sciences Türkiye, İstanbul 34480, Türkiye.ORCID 0000-0003-4351-1719
Gülten ArslanDepartment of Anesthesiology and Reanimation, University of Health Sciences Türkiye, Kartal Dr. Lütfi Kırdar City Hospital, İstanbul 34865, Türkiye.
Seçil Azime KarakuşDepartment of Anesthesiology and Reanimation, University of Health Sciences Türkiye, Kartal Dr. Lütfi Kırdar City Hospital, İstanbul 34865, Türkiye.ORCID 0009-0004-5772-7953
Yekbun BulunDepartment of Anesthesiology and Reanimation, Bingöl State Hospital, Bingöl 12000, Türkiye.
Tomasz GaszynskiDepartment of Anesthesiology and Intensive Therapy, Medical University of Lodz, 90-419 Łódź, Poland.ORCID 0000-0001-5250-3978
Pawel RatajczykDepartment of Anesthesiology and Intensive Therapy, Medical University of Lodz, 90-419 Łódź, Poland.

Funding

Scientific Research Projects Coordination Unit (BAPKO) September 6, 2021, with decision number 2021/157
6 · The paper itself

Abstract

The primary objective of this in vitro study was to prevent the risk of toxicity associated with bupivacaine, widely used in clinical practice, by using magnesium (Mg), a readily available and cost-effective element, as an adjuvant. We hypothesized that Mg might exhibit a protective effect against cytotoxicity in a colon cell culture model under conditions of bupivacaine-induced LAST. Our secondary aim was to investigate its effect on genotoxicity, apoptosis, and iROS. CCD-18Co cells were used in our study. Control group (group C), Bupivacaine group (group B), Magnesium group (group M), and Bupivacaine+Mg group (group BM) were created. The viability of CCD-18Co cells incubated for 24 h in group C was determined to be 100%. These cells were evenly divided, and bupivacaine was administered to group B at concentrations of 5 to 300 μM. In group M, doses of Mg at 0.625 to 320 mEq were added. It was determined that the maximum viability was observed at a Mg dose of 40 mEq (

Indexed as

apoptosisbupivacainecytotoxicityDNA damagemagnesium

Identifiers

PMID39200118
PMCPMC11351263

What OpenQuestion holds

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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.