Evidence map›Paper›PMID 33860456›Full record

ArticleBiological trace element research2022

Brain Boron Level, DNA Content, and Myeloperoxidase Activity of Metformin-Treated Rats in Diabetes and Prostate Cancer Model.

Armagan Begum Ozel, Eda Dagsuyu, Pınar Koroglu Aydın, Ilknur Bugan, Omur Karabulut Bulan, Refiye Yanardag, Aysen Yarat

Abstract read
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Article in Biological trace element research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Trace elements and metal nanoparticles: mechanistic approaches to mitigating chemotherapy-induced toxicity-a review of literature evidence.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
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  11. Article
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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.

Armagan Begum OzelDepartment of Basic Medical Sciences, Biochemistry, Faculty of Dentistry, Marmara University, Basibuyuk Road 9/3 34854 Basibuyuk, Maltepe, Istanbul, Turkey.ORCID https://orcid.org/0000-0002-4197-3103
Eda DagsuyuDepartment of Chemistry, Faculty of Engineering, Istanbul University- Cerrahpasa, Istanbul, Turkey.ORCID https://orcid.org/0000-0003-0395-1058
Pınar Koroglu AydınDepartment of Histology and Embryology, Faculty of Medicine, Halic University, Istanbul, Turkey.ORCID https://orcid.org/0000-0002-3408-7867
Ilknur BuganDepartment of Biology, Faculty of Science, Istanbul University, Istanbul, Turkey.ORCID https://orcid.org/0000-0003-2838-0941
Omur Karabulut BulanDepartment of Biology, Faculty of Science, Istanbul University, Istanbul, Turkey.ORCID https://orcid.org/0000-0002-6591-7317
Refiye YanardagDepartment of Chemistry, Faculty of Engineering, Istanbul University- Cerrahpasa, Istanbul, Turkey.ORCID https://orcid.org/0000-0003-4185-4363
Aysen YaratDepartment of Basic Medical Sciences, Biochemistry, Faculty of Dentistry, Marmara University, Basibuyuk Road 9/3 34854 Basibuyuk, Maltepe, Istanbul, Turkey. ayarat@marmara.edu.tr.ORCID http://orcid.org/0000-0002-8258-6118

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, the effect of metformin on boron levels and oxidative brain damage in rats due to diabetes and prostate cancer was investigated for the first time. Myeloperoxidase (MPO) activity and the amount of DNA were investigated as tissue oxidative and toxic damage parameters. In Copenhagen rats, Dunning prostate cancer was induced using high metastatic MAT-Lylu cells and diabetes was induced by single dose of streptozotocin (STZ) injection. Metformin was administered for 14 days after diabetes and prostate cancer induced. The rats were divided into six groups as follows: control group, diabetic group (D), cancer group (C), diabetic + cancer (DC) group, cancer + metformin (CM) group, diabetic + cancer + metformin (DCM) group. At the end of the experiment, brains were removed. Significant decrease of brain boron levels and significant elevation of MPO activity and DNA levels were observed in D, C, and DC groups as compared to control group. The effect of diabetes induction on the brain boron levels was much more than prostate cancer induction. The administration of metformin with CM and DCM obviously declined MPO activity and increased brain boron levels almost near to control group level. In conclusion, this study shows that the protective effect of metformin against brain damage in STZ-induced diabetic rats with Dunning prostate cancer may also be related to increased boron levels. The boron levels may be a novel indicator of reduced toxic and oxidative stress. Furthermore, the distribution and mechanism of action of boron should be clarified.

Indexed as

Diabetes Mellitus, ExperimentalMetforminProstatic NeoplasmsAnimalsBoronBrainHumansHypoglycemic AgentsMaleOxidative StressPeroxidaseRatsStreptozocinBoronHypoglycemic AgentsMetforminPeroxidaseStreptozocinBoronBrain damageDiabetesDunning prostate cancerMetforminMyeloperoxidase

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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.