Evidence map›Paper›PMID 39206399›Full record

ArticleAdvanced pharmaceutical bulletin2024

Docosahexaenoic Acid Reduced Vascular Endothelial Cell Injury in Diabetic Rats Via the Modulation of Autophagy.

Aysan Eslami Abriz, Atefeh Araghi, Mahdieh Nemati, Maryam Taghavi Narmi, Mahdi Ahmadi, Fatemeh Abedini, Rana Keyhanmanesh, Fariba Ghiasi, Reza Rahbarghazi

Abstract read
In one paragraph

Article in Advanced pharmaceutical bulletin, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

9 authors.

Aysan Eslami AbrizDrug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID https://orcid.org/0009-0001-2975-3220
Atefeh AraghiFaculty of Veterinary Medicine, Amol University of Special Modern Technologies, Amol, Iran.
Mahdieh NematiDrug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Maryam Taghavi NarmiStem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Mahdi AhmadiDrug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Fatemeh AbediniStem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Rana KeyhanmaneshStem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Fariba GhiasiStem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Reza RahbarghaziDrug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID https://orcid.org/0000-0003-3864-9166

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Among varied ω-3 polyunsaturated fatty acid types, the therapeutic properties of docosahexaenoic acid (DHA) have been indicated under diabetic conditions in different cell lineages. Here, we investigated the anti-diabetic properties of DHA in rats with type 2 diabetes mellitus (D2M) focusing on autophagy-controlling factors. Methods: D2M was induced in male Wistar rats using a single dose of streptozocin (STZ) and a high-fat diet for 8 weeks. On week 2, diabetic rats received DHA 950 mg/kg/d until the end of the study. After that, rats were euthanized, and aortic and cardiac tissue samples were stained with H&E staining for histological assessment. The expression of adhesion molecules, ICAM-1 and VCAM-1, was measured in heart samples using real-time PCR analysis. Using western blotting, protein levels of BCLN1, LC3, and P62 were measured in D2M rats pre- and post-DHA treatment. Results: Data showed intracellular lipid vacuoles inside the vascular cells, and cardiomyocytes, after induction of D2M and DHA reduced intracellular lipid droplets and Conclusion: DHA can reduce lipotoxicity of cardiovascular cells possibly via the activation of adaptive autophagy response in D2D rats.

Indexed as

AutophagyDiabetes mellitusDocosahexaenoic acidEndothelial cellsRatsVascular system injuries

Identifiers

PMID39206399
PMCPMC11347735

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.