Evidence map›Paper›PMID 28281693›Full record

ArticleScientific reports2017

Carnosine Attenuates the Development of both Type 2 Diabetes and Diabetic Nephropathy in BTBR ob/ob Mice.

Thomas Albrecht, Maaike Schilperoort, Shiqi Zhang, Jana D Braun, Jiedong Qiu, Angelica Rodriguez, Diego O Pastene, Bernhard K Krämer, Hannes Köppel, Hans Baelde and 8 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 2 pooled it
7.5field-weighted citation impact, top 2% 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

65 citing papers in PubMed, 2 syntheses or guidelines pooled it, 127 citations in OpenAlex.

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  12. 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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5 more citing papers are in PubMed but not listed here.

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

18 authors at 6 institutions in 3 countries.

Thomas AlbrechtDepartment of Nephrology, Endocrinology and Rheumatology, Fifth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Maaike SchilperoortThe Department of Pathology, Leiden University Medical Centre, Leiden, the Netherlands.
Shiqi ZhangDepartment of Nephrology, Endocrinology and Rheumatology, Fifth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Jana D BraunDepartment of Nephrology, Endocrinology and Rheumatology, Fifth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Jiedong QiuDepartment of Nephrology, Endocrinology and Rheumatology, Fifth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Angelica RodriguezDepartment of Nephrology, Endocrinology and Rheumatology, Fifth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Diego O PasteneDepartment of Nephrology, Endocrinology and Rheumatology, Fifth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Bernhard K KrämerDepartment of Nephrology, Endocrinology and Rheumatology, Fifth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Hannes KöppelDepartment of Nephrology, Endocrinology and Rheumatology, Fifth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Hans BaeldeThe Department of Pathology, Leiden University Medical Centre, Leiden, the Netherlands.
Emile de HeerThe Department of Pathology, Leiden University Medical Centre, Leiden, the Netherlands.
Alessandra Anna AltomareThe Department of Pharmaceutical Sciences, University of Milan, Milan, Italy.
Luca RegazzoniThe Department of Pharmaceutical Sciences, University of Milan, Milan, Italy.
Alessandra DenisiThe Department of Pharmaceutical Sciences, University of Milan, Milan, Italy.
Giancarlo AldiniThe Department of Pharmaceutical Sciences, University of Milan, Milan, Italy.
Jacob van den BornDepartment of Nephrology, University Medical Center Groningen, Groningen, the Netherlands.
Benito A YardDepartment of Nephrology, Endocrinology and Rheumatology, Fifth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Sibylle J HauskeDepartment of Nephrology, Endocrinology and Rheumatology, Fifth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
University Medical Centre Mannheim · DEUniversity of Milan · ITLeiden University · NLHeidelberg University · DEUniversity Hospital Heidelberg · DEUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously demonstrated that polymorphisms in the carnosinase-1 gene (CNDP1) determine the risk of nephropathy in type 2 diabetic patients. Carnosine, the substrate of the enzyme encoded by this gene, is considered renoprotective and could possibly be used to treat diabetic nephropathy (DN). In this study, we examined the effect of carnosine treatment in vivo in BTBR (Black and Tan, BRachyuric) ob/ob mice, a type 2 diabetes model which develops a phenotype that closely resembles advanced human DN. Treatment of BTBR ob/ob mice with 4 mM carnosine for 18 weeks reduced plasma glucose and HbA1c, concomitant with elevated insulin and C-peptide levels. Also, albuminuria and kidney weights were reduced in carnosine-treated mice, which showed less glomerular hypertrophy due to a decrease in the surface area of Bowman's capsule and space. Carnosine treatment restored the glomerular ultrastructure without affecting podocyte number, resulted in a modified molecular composition of the expanded mesangial matrix and led to the formation of carnosine-acrolein adducts. Our results demonstrate that treatment with carnosine improves glucose metabolism, albuminuria and pathology in BTBR ob/ob mice. Hence, carnosine could be a novel therapeutic strategy to treat patients with DN and/or be used to prevent DN in patients with diabetes.

Indexed as

Administration, OralAlbuminuriaAnimalsBlood GlucoseCarnosineC-PeptideDiabetes Mellitus, Type 2Diabetic NephropathiesDipeptidasesDisease Models, AnimalGene ExpressionGlomerular MesangiumGlycated HemoglobinHumansHypoglycemic AgentsInsulinaminoacyl-histidine dipeptidaseBlood GlucoseCarnosineC-PeptideDipeptidasesGlycated HemoglobinHypoglycemic AgentsInsulin

Identifiers

PMID28281693
PMCPMC5345040
OpenAlexW2594499858

What OpenQuestion holds

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LicenceCC BY
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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.