Evidence map›Paper›PMID 29205589›Full record

ArticleInternational journal of experimental pathology2017

Carnosine decreased oxidation and glycation products in serum and liver of high-fat diet and low-dose streptozotocin-induced diabetic rats.

Abdurrahman Fatih Aydın, İlknur Bingül, Canan Küçükgergin, Işın Doğan-Ekici, Semra Doğru Abbasoğlu, Müjdat Uysal

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In one paragraph

Article in International journal of experimental pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

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  8. Histidine-Containing Dipeptides in Obesity and Cardiometabolic Health: A Systematic Scoping Review.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
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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

6 authors at 2 institutions in 1 country.

Abdurrahman Fatih AydınIstanbul Medical Faculty, Department of Biochemistry, Istanbul University, Istanbul, Turkey.ORCID 0000-0002-2595-0833
İlknur BingülIstanbul Medical Faculty, Department of Biochemistry, Istanbul University, Istanbul, Turkey.
Canan KüçükgerginIstanbul Medical Faculty, Department of Biochemistry, Istanbul University, Istanbul, Turkey.
Işın Doğan-EkiciDepartment of Pathology, Yeditepe University Medical Faculty, Istanbul, Turkey.
Semra Doğru AbbasoğluIstanbul Medical Faculty, Department of Biochemistry, Istanbul University, Istanbul, Turkey.
Müjdat UysalIstanbul Medical Faculty, Department of Biochemistry, Istanbul University, Istanbul, Turkey.
Istanbul University · TRYeditepe University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-fat diet (HFD) and low-dose streptozotocin (STZ)-treated rats provide useful animal model for type II diabetes mellitus. Oxidative stress and advanced glycation end products (AGEs) play a role in the development of diabetic complications. Carnosine (CAR) has anti-oxidant and anti-glycating properties. We investigated the effects of CAR on oxidation and glycation products in HFD+STZ rats. Rats were fed with HFD (60% of total calories from fat) for 4 weeks, and then a single dose of STZ (40 mg/kg; i.p.) was applied. Rats with blood glucose levels above 200 mg/dl were fed with HFD until the end of the 12th week. CAR (250 mg/kg body weight; i.p.; five times a week) was administered to the rats for the last four weeks. CAR significantly decreased serum triglyceride (TG) (57.7%), cholesterol (35.6%) levels and hepatic marker enzyme activities of HFD+STZ rats. It significantly reduced serum reactive oxygen species (ROS) (23.7%), AGEs (13.4%) and advanced oxidized protein products (AOPP) (35.9%) and hepatic TG (59%), ROS (26%), malondialdehyde (MDA) (11.5%), protein carbonyl (PC) (19.2%) and AGE (20.2%) levels. Liver steatosis and hepatocyte ballooning were also significantly reduced. However, CAR treatment did not alter serum glucose and blood glycated haemoglobin and hepatic anti-oxidant enzyme activities/mRNA expressions in HFD+STZ rats. Our results indicate that CAR decreased accumulation of oxidation and glycation products, such as MDA, AGE, AOPP and PC in the serum and liver and ameliorated hepatic dysfunction in HFD+STZ rats. This effect may be related to its anti-oxidative, anti-glycating, and anti-lipogenic potential.

Indexed as

AnimalsAntioxidantsBlood GlucoseBody WeightCarnosineCholesterolDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Diet, High-FatDrug Evaluation, PreclinicalGlycated HemoglobinGlycation End Products, AdvancedLiverMaleOrgan SizeOxidation-ReductionAntioxidantsBlood GlucoseCarnosineCholesterolGlycated HemoglobinGlycation End Products, AdvancedReactive Oxygen SpeciesStreptozocinTriglyceridesadvanced glycation end productsCarnosinediabetes mellitusoxidative stress

Identifiers

PMID29205589
PMCPMC5743804
OpenAlexW2773250050

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.