Evidence map›Paper›PMID 32714041›Full record

ArticleSaudi journal of biological sciences2020

Morin attenuates STZ-induced diabetic retinopathy in experimental animals.

Bo Jiang, Qingsen Geng, Tao Li, Sayeed Mohammad Firdous, Xiaodong Zhou

Open access · hybridAbstract read
In one paragraph

Article in Saudi journal of biological sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Antioxidants Isolated fromMolecules (Basel, Switzerland) · 2021
    Article
  8. 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

5 authors at 2 institutions in 1 country.

Bo JiangDepartment of Ophthalmology, Jinshan Hospital of Fudan University, Jinshan District, Shanghai 201508, China.
Qingsen GengDepartment of Eye Fundus,Liaocheng Guangming Ophthalmological Hospital, Liaocheng, Shandong 252000, China.
Tao LiDepartment of Ophthalmology, Jinshan Hospital of Fudan University, Jinshan District, Shanghai 201508, China.
Sayeed Mohammad FirdousDepartment of Pharmacology, Calcutta Institute of Pharmaceutical Technology & AHS, Uluberia, Howrah 711316, West Bengal, India.
Xiaodong ZhouDepartment of Ophthalmology, Jinshan Hospital of Fudan University, Jinshan District, Shanghai 201508, China.
Jinshan Hospital of Fudan University · CNLiaocheng People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic retinopathy (DR) occurs in untreated diabetic patients due to the strong influence of oxidative stress. Bioflavonoids are well known for their antioxidant property. Morin, a bioflavonoid, has been demonstrated for its antioxidant as well as antidiabetic activity. Thus, this research work intended to determine the ameliorative impact of morin in DR rats using STZ-induced type 1 diabetic model. To induce type 1 diabetic in rats STZ (60 mg/kg) was administered intraperitoneally. Grouping of animals was done as described below (n = 6), where, group I - normal control, group II - diabetic control, group III - morin (25 mg/kg), group IV - morin (50 mg/kg), and group V - metformin (350 mg/kg) were used. All the animals underwent treatment for 60 days as given above. It was observed that supplementation of morin (25 and 50 mg/kg) showed a noteworthy decline in elevated serum glucose level. Moreover, decrease in the level of LPO and improved activity of endogenous antioxidants (GPx, CAT, and SOD) was observed in morin treated groups. It also notably drops the concentration of TNF-α, IL-1β, and VEGF in the tissue homogenate of the retina. Furthermore, it increased the retinal thickness and cell count in the ganglion cell layer of the retina in diabetic animals. Hence, we can conclude that morin encumbers the progression of DR in diabetic animals, which may be via antioxidant property and suppression of TNF-α, IL-1β, and VEGF.

Indexed as

AGEs, Advanced glycated end productsAntioxidantsBGL, Blood glucose levelBRB, Blood retinal barrierCAT, CatalaseDAG, DiacylglycerolDiabetic retinopathyGPx, Glutathione peroxidaseIL-1β and VEGFIL-1β, Interleukin 1 betaLPO, Lipid peroxidaseMorinPKC, Protein kinase CROS, Reactive oxygen speciesSOD, Superoxide dismutaseSTZ, StreptozotocinTNF-αTNF-α, Tumor necrosis factor alphaVEGF, Vascular endothelial growth factor

Identifiers

PMID32714041
PMCPMC7376113
OpenAlexW3037320348

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.