Evidence map›Paper›PMID 26821002›Full record

ArticleMolecules (Basel, Switzerland)2016

Inhibitory Effect of Crocin(s) on Lens α-Crystallin Glycation and Aggregation, Results in the Decrease of the Risk of Diabetic Cataract.

Fereshteh Bahmani, Seyedeh Zahra Bathaie, Seyed Javid Aldavood, Arezou Ghahghaei

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  3. Metabolic memory: mechanisms and diseases.Signal transduction and targeted therapy · 2024
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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

4 authors at 3 institutions in 1 country.

Fereshteh BahmaniDepartment of Clinical Biochemistry, Faculty of Medical Sciences, Tarbiat Modares University (TMU), Tehran P. O. Box 14115-111, Iran. bahmani@kaums.ac.ir.
Seyedeh Zahra BathaieDepartment of Clinical Biochemistry, Faculty of Medical Sciences, Tarbiat Modares University (TMU), Tehran P. O. Box 14115-111, Iran. bathai_z@modares.ac.ir.
Seyed Javid AldavoodDepartment of Clinical Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran P. O. Box 14185-746, Iran. sja@ut.ac.ir.
Arezou GhahghaeiDepartment of Biology, Faculty of Science, University of Sistan and Baluchestan, Zahedan P. O. Box 98167, Iran. arezou@chem.usb.ac.ir.
Tarbiat Modares University · IRUniversity of Sistan and Baluchestan · IRUniversity of Tehran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current study investigates the inhibitory effect of crocin(s), also known as saffron apocarotenoids, on protein glycation and aggregation in diabetic rats, and α-crystallin glycation. Thus, crocin(s) were administered by intraperitoneal injection to normal and streptozotocin-induced diabetic rats. The cataract progression was recorded regularly every two weeks and was classified into four stages. After eight weeks, the animals were sacrificed and the parameters involved in the cataract formation were measured in the animal lenses. Some parameters were also determined in the serum and blood of the rats. In addition, the effect of crocin(s) on the structure and chaperone activity of α-crystallin in the presence of glucose was studied by different methods. Crocin(s) lowered serum glucose levels of diabetic rats and effectively maintained plasma total antioxidants, glutathione levels and catalase activity in the lens of the animals. In the in vitro study, crocin(s) inhibited α-crystallin glycation and aggregation. Advanced glycation end products fluorescence, hydrophobicity and protein cross-links were also decreased in the presence of crocin(s). In addition, the decreased chaperone activity of α-crystallin in the presence of glucose changed and became close to the native value by the addition of crocin(s) in the medium. Crocin(s) thus showed a powerful inhibitory effect on α-crystallin glycation and preserved the structure-function of this protein. Crocin(s) also showed the beneficial effects on prevention of diabetic cataract.

Indexed as

alpha-CrystallinsAnimalsBlood GlucoseCarotenoidsCataractCell AggregationDiabetes Mellitus, ExperimentalDisease ProgressionGlycation End Products, AdvancedInjections, IntraperitonealRatsStreptozocinalpha-CrystallinsBlood GlucoseCarotenoidscrocinGlycation End Products, AdvancedStreptozocincataractcrocin(s)glycationoxidative stressstreptozotocinstructure-function

Identifiers

PMID26821002
PMCPMC6273448
OpenAlexW2272305194

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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.