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Carnosine treatment largely prevents alterations of renal carnosine metabolism in diabetic mice

Peters V, Schmitt CP, Zschocke J, Gross ML, Brismar K, Forsberg E. Amino Acids, 2012; 42(6):2411-2416 (online 2011).

Controlled trialOther animals

Design
Controlled trial
Subjects
not stated in abstract (db/db diabetic mice and controls)
Dose used in the study
not stated in abstract
Duration
4 weeks of carnosine treatment
What was measured
Kidney carnosinase (CN1) activity, renal carnosine, anserine and homocarnosine, proteinuria and vascular permeability in db/db mice and controls.

What the authors reported

Kidney CN1 activity increased with age and was significantly higher in diabetic mice than controls. Renal carnosine was unaffected, but anserine was tenfold lower in db/db mice (0.24 +/- 0.2 vs 2.28 +/- 0.3 nmol/mg protein, p < 0.001); homocarnosine was low in both groups. Four weeks of carnosine decreased CN1 activity in diabetic mice (0.32 to 0.05, p < 0.01) to close to normal, raised renal anserine (0.24 to 5.7, p < 0.01) and left carnosine unchanged (53 vs 61 nmol/mg protein, not significant). It also halved proteinuria and reduced vascular permeability to one-fifth. The authors conclude carnosine largely prevents the alterations of renal carnosine metabolism.

Limits of this study

Mouse model; dose, route and group sizes not given in the abstract; units reported in the abstract are inconsistent between measures. Full text not read. Route of carnosine not stated in abstract; rodents lack serum carnosinase, so oral results do not carry over to people.

Source

PubMed 21833769 · doi:10.1007/s00726-011-1046-4

Entry checked against PubMed abstract (E-utilities) on 2026-10-19. The dose shown is the dose the researchers used. It is not a recommendation. How to read this page.