Evidence map›Paper›PMID 31705353›Full record

ArticleInflammation2020

Nobiletin Protects from Renal Ischemia-Reperfusion Injury in Rats by Suppressing Inflammatory Cytokines and Regulating iNOS-eNOS Expressions.

Mehmet Güvenç, Mustafa Cellat, Ahmet Uyar, Hüseyin Özkan, İshak Gokcek, Cafer Tayer İsler, Akın Yakan

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.7field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Does Ambroxol alleviate kidney ischemia-reperfusion injury in rats?Iranian journal of basic medical sciences · 2022
    Article
  12. Nobiletin prevents amyloid βMetabolic brain disease · 2022
    Article
  13. Article
  14. Review
  15. Article
  16. Frontiers in nutrition · 2021
    Article
  17. Systematically Deciphering the Pharmacological Mechanism of Fructus Aurantii via Network Pharmacology.Evidence-based complementary and alternative medicine : eCAM · 2021
    Article
  18. Article
  19. Review
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.

Mehmet GüvençMustafa Kemal University, Faculty of Veterinary Medicine, Department of Physiology, Antakya, Turkey. mguvenc@mku.edu.tr.ORCID http://orcid.org/0000-0002-9716-0697
Mustafa CellatMustafa Kemal University, Faculty of Veterinary Medicine, Department of Physiology, Antakya, Turkey.
Ahmet UyarMustafa Kemal University, Faculty of Veterinary Medicine, Department of Pathology, Antakya, Turkey.
Hüseyin ÖzkanMustafa Kemal University, Faculty of Veterinary Medicine, Department of Genetics, Antakya, Turkey.
İshak GokcekMustafa Kemal University, Faculty of Veterinary Medicine, Department of Physiology, Antakya, Turkey.
Cafer Tayer İslerMustafa Kemal University, Faculty of Veterinary Medicine, Department Surgery, Antakya, Turkey.
Akın YakanMustafa Kemal University, Faculty of Veterinary Medicine, Department of Genetics, Antakya, Turkey.
Mustafa Kemal University · TR

Funding

Mustafa Kemal Üniversitesi 17.M.005
6 · The paper itself

Abstract

Ischemia-reperfusion injury is an organ failure caused by hypoxia and reperfusion, which is closely associated with oxidative stress and inflammation. In this study, we investigated whether nobiletin had protective effects on inflammatory parameters, oxidative damage, iNOS-eNOS expressions, and histopathological structure of renal tissue in rats with renal ischemia-reperfusion injury. For this purpose, 24 rats were divided into 4 groups: group 1 (Control), group 2 (Ischemia-Reperfusion-IR), group 3 (Nobiletin-10 mg/kg p.o.), group 4 (Nobiletin + IR). The study was continued for 7 days. At the end of the study, urea (p < 0.05), creatine (p < 0.05), MDA (p < 0.001), TNF-alpha (p < 0.001), IL-1 beta (p < 0.05), and IL-6 (p < 0.001) levels increased in the IR group; however, a significant decrease occurred in group 4 (Nobiletin + IR) and it reached the control group levels. In the IR group, GSH (p < 0.01) levels, and GSH.Px (p < 0.01) and CAT (p < 0.05) activities decreased whereas they increased significantly in group 4 (Nobiletin + IR) and reached the same levels as the control group. In histopathological analyses, destruction and increased iNOS-eNOS expressions in the IR group showed a significant decrease in group 4 (Nobiletin + IR). As a result, the application of nobiletin has shown that it has protective effects by reducing kidney damage caused by IR injury.

Indexed as

AnimalsAnti-Inflammatory AgentsCytokinesDisease Models, AnimalFlavonesInflammation MediatorsKidneyKidney DiseasesMaleNitric Oxide Synthase Type IINitric Oxide Synthase Type IIIRats, WistarReperfusion InjurySignal TransductionAnti-Inflammatory AgentsCytokinesFlavonesInflammation MediatorsNitric Oxide Synthase Type IINitric Oxide Synthase Type IIInobiletinNos2 protein, ratNos3 protein, ratinflammationiNOS-eNOSischemia-reperfusionnobiletin

Identifiers

PMID31705353
OpenAlexW2983731252

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.