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Kefir administration reduced progression of renal injury in STZ-diabetic rats by lowering oxidative stress.
- Source :
-
Nitric oxide : biology and chemistry [Nitric Oxide] 2014 Feb 15; Vol. 37, pp. 53-60. Date of Electronic Publication: 2014 Jan 06. - Publication Year :
- 2014
-
Abstract
- This study aimed at assessing the effects of Kefir, a probiotic fermented milk, on oxidative stress in diabetic animals. The induction of diabetes was achieved in adult male Wistar rats using streptozotocin (STZ). The animals were distributed into four groups as follows: control (CTL); control Kefir (CTLK); diabetic (DM) and diabetic Kefir (DMK). Starting on the 5th day of diabetes, Kefir was administered by daily gavage at a dose of 1.8 mL/day for 8 weeks. Before and after Kefir treatment, the rats were placed in individual metabolic cages to obtain blood and urine samples to evaluate urea, creatinine, proteinuria, nitric oxide (NO), thiobarbituric acid reactive substances (TBARS) and C-reactive protein (CRP). After sacrificing the animals, the renal cortex was removed for histology, oxidative stress and NOS evaluation. When compared to CTL rats, DM rats showed increased levels of glycemia, plasmatic urea, proteinuria, renal NO, superoxide anion, TBARS, and plasmatic CRP; also demonstrated a reduction in urinary urea, creatinine, and NO. However, DMK rats showed a significant improvement in most of these parameters. Despite the lack of differences observed in the expression of endothelial NO synthase (eNOS), the expression of inducible NO synthase (iNOS) was significantly lower in the DMK group when compared to DM rats, as assessed by Western blot analysis. Moreover, the DMK group presented a significant reduction of glycogen accumulation within the renal tubules when compared to the DM group. These results indicate that Kefir treatment may contribute to better control of glycemia and oxidative stress, which is associated with the amelioration of renal function, suggesting its use as a non-pharmacological adjuvant to delay the progression of diabetic complications.<br /> (Copyright © 2014 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Diabetes Mellitus, Experimental chemically induced
Diabetes Mellitus, Experimental metabolism
Diabetes Mellitus, Type 1 chemically induced
Diabetes Mellitus, Type 1 metabolism
Glucose Tolerance Test
Glycogen metabolism
Hyperglycemia diet therapy
Kidney Diseases metabolism
Kidney Diseases pathology
Kidney Tubules drug effects
Kidney Tubules enzymology
Kidney Tubules metabolism
Kidney Tubules pathology
Male
Nitric Oxide metabolism
Probiotics pharmacology
Probiotics therapeutic use
Rats
Rats, Wistar
Streptozocin
Cultured Milk Products
Diabetes Mellitus, Experimental complications
Diabetes Mellitus, Type 1 complications
Disease Progression
Kidney Diseases complications
Kidney Diseases diet therapy
Oxidative Stress drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1089-8611
- Volume :
- 37
- Database :
- MEDLINE
- Journal :
- Nitric oxide : biology and chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 24406684
- Full Text :
- https://doi.org/10.1016/j.niox.2013.12.012