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Study · Animal study (in vivo) · mouse · 2017

13 results

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

Albrecht T, Schilperoort M, Zhang S, Braun JD, Qiu J, Rodriguez A, Pastene DO, Krämer BK, Köppel H, Baelde H, de Heer E, Anna Altomare A and 6 more

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Regazzoni L, Denisi A, Aldini G, van den Born J, Yard BA, Hauske SJ

Scientific reports10 Mar 2017Cited by 105 (Europe PMC)

Summary

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.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study13

13 results from studies that gave the peptide. No result from this study comes from people.

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine reduced plasma glucose.

    In plain wordsIn mice with diabetes, carnosine reduced plasma glucose.

    Outcome
    DecreasePlasma glucose
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine reduced HbA1c.

    In plain wordsIn mice with diabetes, carnosine reduced HbA1c.

    Outcome
    DecreaseHbA1c
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine elevated insulin levels.

    In plain wordsIn mice with diabetes, carnosine increased insulin levels.

    Outcome
    IncreaseInsulin
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine elevated C-peptide levels.

    In plain wordsIn mice with diabetes, carnosine increased C-peptide levels.

    Outcome
    IncreaseC-peptide
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine reduced albuminuria.

    In plain wordsIn mice with diabetes, carnosine reduced urine albumin.

    Outcome
    DecreaseAlbuminuria
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  6. 06AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine reduced kidney weights.

    In plain wordsIn mice with diabetes, carnosine reduced kidney weights.

    Outcome
    DecreaseKidney weight
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  7. 07AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine reduced glomerular hypertrophy.

    In plain wordsIn mice with diabetes, carnosine reduced enlargement of kidney filtering structures.

    Outcome
    DecreaseGlomerular hypertrophy
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  8. 08AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine reduced the surface area of Bowman's capsule.

    In plain wordsIn mice with diabetes, carnosine reduced the surface area of Bowman's capsule in the kidney.

    Outcome
    DecreaseBowman capsule surface area
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  9. 09AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine reduced the surface area of Bowman's space.

    In plain wordsIn mice with diabetes, carnosine reduced the surface area of Bowman's space in the kidney.

    Outcome
    DecreaseBowman space surface area
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  10. 10AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine restored glomerular ultrastructure.

    In plain wordsIn mice with diabetes, carnosine restored the fine structure of kidney filtering units.

    Outcome
    Direction not reportedGlomerular ultrastructure
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  11. 11AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine did not affect podocyte number.

    In plain wordsIn mice with diabetes, carnosine did not change podocyte number.

    Outcome
    No significant changePodocyte number
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  12. 12AnimalAnimal study (in vivo)Efficacy outcome

    In BTBR ob/ob mice, carnosine modified the molecular composition of the expanded mesangial matrix.

    In plain wordsIn mice with diabetes, carnosine changed the molecular composition of the expanded kidney mesangial matrix.

    Outcome
    Direction not reportedMesangial matrix molecular composition
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Kidney function · Kidney and urinary
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.
  13. 13AnimalAnimal study (in vivo)Mechanism

    In BTBR ob/ob mice, carnosine treatment led to carnosine-acrolein adduct formation.

    In plain wordsIn mice with diabetes, carnosine treatment produced carnosine-acrolein adducts.

    Outcome
    IncreaseCarnosine-acrolein adduct formation
    Study

    micen: not reported in source

    BTBR ob/ob type 2 diabetes model
    Outcome group
    Receptor activity and mechanism · Kidney and urinary
    Studied dose
    4 mM · 18 weeksAs given in this study (mice).

    Source sentences

    Summary
    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.
    1 context sentence
    Summary · context
    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.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    27 Oct 2026, 18:20 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:32 UTC

    First added · source update from Europe PMC

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