Plasma and erythrocyte glutathione peroxidase activity, serum selenium concentration, and plasma total antioxidant capacity in cats with IRIS stages I-IV chronic kidney disease
- PMID: 24341729
- PMCID: PMC4895542
- DOI: 10.1111/jvim.12264
Plasma and erythrocyte glutathione peroxidase activity, serum selenium concentration, and plasma total antioxidant capacity in cats with IRIS stages I-IV chronic kidney disease
Abstract
Background: Serum selenium concentrations and the activity of plasma glutathione peroxidase (GPx) decrease with the progression of chronic kidney disease (CKD) in human patients. Selenium is considered a limiting factor for plasma GPx synthesis. Plasma total antioxidant capacity (TAC) is decreased in CKD cats in comparison to healthy cats.
Hypothesis: Serum selenium concentrations and plasma and erythrocyte GPx activity in cats with CKD are lower than in healthy cats. Serum selenium concentrations, the activity of enzymes, and plasma TAC progressively decrease with the progression of kidney disease according to IRIS (International Renal Interest Society) classification.
Animals: Twenty-six client-owned cats in IRIS stages I-IV of CKD were compared with 19 client-owned healthy cats.
Methods: A CBC, serum biochemical profile, urinalysis, plasma and erythrocyte GPx activity, serum selenium concentration, and plasma TAC were measured in each cat.
Results: Cats in IRIS stage IV CKD had a significantly higher (P = .025) activity of plasma GPx (23.44 ± 6.28 U/mL) than cats in the control group (17.51 ± 3.75 U/mL). There were no significant differences in erythrocyte GPx, serum selenium concentration, and plasma TAC, either among IRIS stages I-IV CKD cats or between CKD cats and healthy cats.
Conclusions and clinical importance: Erythrocyte GPx activity, serum selenium concentration, and plasma TAC do not change in CKD cats compared with healthy cats. Selenium is not a limiting factor in feline CKD. Increased plasma GPx activity in cats with stage IV CKD suggests induction of antioxidant defense mechanisms. Antioxidant defense systems might not be exhausted in CKD in cats.
Keywords: Antioxidants; Cats; Oxidative stress; Renal failure.
Copyright © 2013 by the American College of Veterinary Internal Medicine.
Similar articles
-
Red blood cell and plasma glutathione peroxidase activities and selenium concentration in patients with chronic kidney disease: a review.Acta Biochim Pol. 2006;53(4):663-77. Epub 2006 Dec 11. Acta Biochim Pol. 2006. PMID: 17160142 Review.
-
Preliminary evaluation of fecal fatty acid concentrations in cats with chronic kidney disease and correlation with indoxyl sulfate and p-cresol sulfate.J Vet Intern Med. 2020 Jan;34(1):206-215. doi: 10.1111/jvim.15634. Epub 2019 Nov 6. J Vet Intern Med. 2020. PMID: 31693251 Free PMC article.
-
Supplementation of vitamin E as an addition to a commercial renal diet does not prolong survival of cats with chronic kidney disease.BMC Vet Res. 2024 Jul 10;20(1):308. doi: 10.1186/s12917-024-04176-8. BMC Vet Res. 2024. PMID: 38987749 Free PMC article.
-
The fecal microbiome and serum concentrations of indoxyl sulfate and p-cresol sulfate in cats with chronic kidney disease.J Vet Intern Med. 2019 Mar;33(2):662-669. doi: 10.1111/jvim.15389. Epub 2018 Dec 18. J Vet Intern Med. 2019. PMID: 30561098 Free PMC article.
-
Selenium and selenium-dependent antioxidants in chronic kidney disease.Adv Clin Chem. 2015;68:131-51. doi: 10.1016/bs.acc.2014.11.006. Epub 2015 Jan 7. Adv Clin Chem. 2015. PMID: 25858871 Review.
Cited by
-
Vitamin E supplementation fails to impact measures of oxidative stress or the anaemia of feline chronic kidney disease: a randomised, double-blinded placebo control study.Vet Med Sci. 2016 Jan 22;2(2):117-124. doi: 10.1002/vms3.21. eCollection 2016 May. Vet Med Sci. 2016. PMID: 29067185 Free PMC article.
-
Investigation of hallmarks of carbonyl stress and formation of end products in feline chronic kidney disease as markers of uraemic toxins.J Feline Med Surg. 2019 Jun;21(6):465-474. doi: 10.1177/1098612X18783858. Epub 2018 Jul 17. J Feline Med Surg. 2019. PMID: 30015556 Free PMC article.
-
ISFM Consensus Guidelines on the Diagnosis and Management of Feline Chronic Kidney Disease.J Feline Med Surg. 2016 Mar;18(3):219-39. doi: 10.1177/1098612X16631234. J Feline Med Surg. 2016. PMID: 26936494 Free PMC article.
-
Evaluation of Electrolyte Concentration and Pro-Inflammatory and Oxidative Status in Dogs with Advanced Chronic Kidney Disease under Dietary Treatment.Toxins (Basel). 2019 Dec 19;12(1):3. doi: 10.3390/toxins12010003. Toxins (Basel). 2019. PMID: 31861622 Free PMC article.
-
Reactive oxygen species, glutathione, and vitamin E concentrations in dogs with hemolytic or nonhemolytic anemia.J Vet Intern Med. 2020 Nov;34(6):2357-2364. doi: 10.1111/jvim.15926. Epub 2020 Oct 13. J Vet Intern Med. 2020. PMID: 33047374 Free PMC article.
References
-
- King JN, Tasker S, Gunn‐Moore DA, et al. Prognostic factors in cats with chronic kidney disease. J Vet Intern Med 2007;21:906–916. - PubMed
-
- Polzin DJ. Chronic kidney disease In: Ettinger SJ, Feldman EC, eds. Textbook of Veterinary Internal Medicine, 7th ed St Louis, MO: Saunders; 2010:2036–2067.
-
- Ceballos‐Picot I, Witko‐Sarsat V, Merad‐Boudia M, et al. Glutathione antioxidant system as a marker of oxidative stress in chronic renal failure. Free Radic Biol Med 1996;21:845–853. - PubMed
-
- Galle J. Oxidative stress in chronic renal failure. Nephrol Dial Transplant 2001;16:2135–2137. - PubMed
-
- Wardle EN. Cellular oxidative processes in relation to renal disease. Am J Nephrol 2005;25:13–22. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous
