Blood plasma and urinary biomarkers of oxidative stress in cats with urethral obstruction.


Journal

BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759

Informations de publication

Date de publication:
27 Apr 2024
Historique:
received: 20 12 2023
accepted: 08 04 2024
medline: 28 4 2024
pubmed: 28 4 2024
entrez: 27 4 2024
Statut: epublish

Résumé

This study aimed to investigate variations of the oxidative status in cats affected by urethral obstruction (UO) under Feline Idiopathic Cystitis (FIC) and Bacterial Cystitis (BC), in comparison with a group of healthy subjects. In both groups, the levels of several markers (either direct or indirect) indicative of the oxidative attack and of the antioxidant response were analyzed on plasma and urine samples. In particular, the plasma samples were evaluated for nitric oxide (NO), hydroperoxides derived by reactive oxygen activity (d-ROMs test), superoxide anion (O The analytical data on plasma showed that UO, independently of the FIC or BC etiology, induced the insurgence of oxidative stress conditions at the systemic level. In the urine of the UO patients, except for SOD that increased, the markers of redox status were markedly decreased due probably their compromised filtration, thus suggesting involvement of renal function (assessed also by the high levels of plasma creatinine and proteinuria) with no oxidative damage of the lower urinary tract. Moreover, the adoption of a novel oxidative stress index' (OSI) allowed to establish, by means of a numerical value, the different degrees of oxidative stress conditions for single UO patients, both in terms of oxidative attack and antioxidant response. Feline urethral obstruction, induced by Idiopathic Cystitis and Bacterial Cystitis, causes oxidative stress conditions at the systemic level that do not interest the lower urinary tract. Despite to the high variability of the profiles of oxidative stress indexes both in healthy and UO patients, the determination of OSI made possible the evaluation of their single degrees of oxidative stress. Possibly the results of this investigation can be compared with those of correspondent pathologies both in humans and in other animal species.

Sections du résumé

BACKGROUND BACKGROUND
This study aimed to investigate variations of the oxidative status in cats affected by urethral obstruction (UO) under Feline Idiopathic Cystitis (FIC) and Bacterial Cystitis (BC), in comparison with a group of healthy subjects. In both groups, the levels of several markers (either direct or indirect) indicative of the oxidative attack and of the antioxidant response were analyzed on plasma and urine samples. In particular, the plasma samples were evaluated for nitric oxide (NO), hydroperoxides derived by reactive oxygen activity (d-ROMs test), superoxide anion (O
RESULTS RESULTS
The analytical data on plasma showed that UO, independently of the FIC or BC etiology, induced the insurgence of oxidative stress conditions at the systemic level. In the urine of the UO patients, except for SOD that increased, the markers of redox status were markedly decreased due probably their compromised filtration, thus suggesting involvement of renal function (assessed also by the high levels of plasma creatinine and proteinuria) with no oxidative damage of the lower urinary tract. Moreover, the adoption of a novel oxidative stress index' (OSI) allowed to establish, by means of a numerical value, the different degrees of oxidative stress conditions for single UO patients, both in terms of oxidative attack and antioxidant response.
CONCLUSIONS CONCLUSIONS
Feline urethral obstruction, induced by Idiopathic Cystitis and Bacterial Cystitis, causes oxidative stress conditions at the systemic level that do not interest the lower urinary tract. Despite to the high variability of the profiles of oxidative stress indexes both in healthy and UO patients, the determination of OSI made possible the evaluation of their single degrees of oxidative stress. Possibly the results of this investigation can be compared with those of correspondent pathologies both in humans and in other animal species.

Identifiants

pubmed: 38678221
doi: 10.1186/s12917-024-04009-8
pii: 10.1186/s12917-024-04009-8
doi:

Substances chimiques

Biomarkers 0
8-Hydroxy-2'-Deoxyguanosine 88847-89-6
Superoxide Dismutase EC 1.15.1.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

163

Informations de copyright

© 2024. The Author(s).

Références

Jukes A, Lui M, Morton JM, Marshall R, Yeow N, Gunew M. Associations between increased body condition score, bodyweight, age and breed with urethral obstruction in male castrated cats. Vet J. 2019;244:7–12.
doi: 10.1016/j.tvjl.2018.11.018 pubmed: 30825898
Cooper ES. Controversies in the management of feline urethral obstruction. J Vet Emerg Crit Care. 2015;25(1):130–7. https://doi.org/10.1111/vec.12278 .
doi: 10.1111/vec.12278
Forrestier SD, Towell TL. Feline idiopathic cystitis. Vet Clin North Am Small Anim Pract. 2015;45:783–806.
doi: 10.1016/j.cvsm.2015.02.007
Vieira ANLS, Ramos PRR, Melchert A, Okamoto PTCG. Feline Pandora’s syndrome: a bibliographic review. Vet e Zootec. 2017;24(4):680–90.
doi: 10.35172/rvz.2017.v24.239
Parys M, Yuzbasiyan-Gurkan V, Kruger JM. Serum cytokine profiling in cats with Acute Idiopathic Cystitis. J Vet Intern Med. 2018;32:274–x279.
doi: 10.1111/jvim.15032 pubmed: 29356123 pmcid: 5787166
He C, Fan K, Hao Z, Tang N, Li G, Wang S, Prevalence. Risk factors, pathophysiology, potential biomarkers and management of Feline Idiopathic Cystitis: an Update Review. Front Vet Sci. 2022;9:900847. https://doi.org/10.3389/fvets.2022.900847 .
doi: 10.3389/fvets.2022.900847 pubmed: 35812890 pmcid: 9257190
Byron JK. Urinary tract infection. Vet Clin North Am Small Anim Pract. 2019;49(2):211–21.
doi: 10.1016/j.cvsm.2018.11.005 pubmed: 30591189
Weese JS, Blondeau J, Boothe D, Guardabassi LG, Gumley N, Papich M, Jessen LR, Lappin M, Rankin S, Westropp JL, Sykes J. International Society for Companion Animal Infectious Diseases (ISCAID) guidelines for the diagnosis and management of bacterial urinary tract infections in dogs and cats. Vet J. 2019;247:8–25.
doi: 10.1016/j.tvjl.2019.02.008 pubmed: 30971357
Litster A, Moss S, Platell J, Trott DJ. Occult bacterial lower urinary tract infections in cats—urinalysis and culture findings. Vet Microbiol. 2009;136(1–2):130–4.
doi: 10.1016/j.vetmic.2008.10.019 pubmed: 19056189
Rieser TM. Urinary tract emergencies. Vet Clin North Am Small Anim Pract. 2005;35:359–73.
doi: 10.1016/j.cvsm.2004.12.001 pubmed: 15698915
Fröhlich L, Hartmann K, Sautter-Louis C, Dorsch R. Postobstructive diuresis in cats with naturally occurring lower urinary tract obstruction: incidence, severity and association with laboratory parameters on admission. J Feline Med Surg. 2016;18(10):809–17.
doi: 10.1177/1098612X15594842 pubmed: 26179575
Gülersoy E, Maden M, Parlak TM, Sayin Z. Diagnostic effectiveness of stress biomarkers in cats with feline interstitial and bacterial cystitis. Vet Clin Pathol. 2023;52:88–96. https://doi.org/10.1111/vcp.13173 .
doi: 10.1111/vcp.13173 pubmed: 36436835
Kullmann FA, McDonnell BM, Wolf-Johnston AS, Lynn AM, Giglio D, Getchell SE, Ruiz WG, Zabbarova IV, Ikeda Y, Kanai AJ, Roppolo JR, Bastacky SI, Apodaca G, Buffington CAT, Birder LA. Inflammation and tissue remodeling in the bladder and urethra in feline interstitial cystitis. Front Syst Neurosci. 2018;12:13. https://doi.org/10.3389/fnsys.2018.00013 .
doi: 10.3389/fnsys.2018.00013 pubmed: 29706873 pmcid: 5908978
Hostutler RA, Chew DJ, DiBartola SP. Recent concepts in feline lower urinary tract disease. Vet Clin North Am Small Anim Pract. 2005;35:147–70. https://doi.org/10.1016/j.cvsm.2004.08.006 .
doi: 10.1016/j.cvsm.2004.08.006 pubmed: 15627632
Jones E, Palmieri C, Thompson M, Jackson K, Allavena R. Feline Idiopathic Cystitis: Pathogenesis, Histopathology and Comparative Potential. J Comp Pathol. 2021;185:18–29. https://doi.org/10.1016/j.jcpa.2021.03.006 . Epub 2021 Apr 16. PMID: 34119228.
Ener K, Keske M, Aldemir M, Fuat Özcan M, Okulu E, Özayar A, Ergin M, Gökhan Doluoglu O, Çakmak S, Erel O. Evaluation of oxidative stress status and antioxidant capacity in patients with painful bladder syndrome/interstitial cystitis: preliminary results of a randomised study. Int Urol Nephrol. 2015;47:1297–302. https://doi.org/10.1007/s11255-015-1021-1 .
doi: 10.1007/s11255-015-1021-1 pubmed: 26049975
Michalek M, Tabis A, Paslawska U, Noszcyk-Nowak A. Antioxidant defence and oxidative stress markers in cats with asymptomatic and symptomatic hypertrophic cardiomyopathy: a pilot study. BMC Vet Res. 2020;16:26. https://doi.org/10.1186/s1291-020-2256-3 .
doi: 10.1186/s1291-020-2256-3 pubmed: 32000761 pmcid: 6990494
Gessner DK, Ringseis R, Eder K. Potential of plant polyphenols to combat oxidative stress and inflammatory processes in farm animals. J Anim Physiol Anim Nutr. 2017;101:605–28. https://doi.org/10.1111/jpn.12579 .
doi: 10.1111/jpn.12579
Cucchi A, Ramoni R, Basini G, Bussolati S, Quintavalla F. Oxidant–antioxidant status in Canine Multicentric Lymphoma and primary cutaneous mastocytoma. Processes. 2020;8:802. https://doi.org/10.3390/pr8070802 .
doi: 10.3390/pr8070802
Molinari L, Basini G, Ramoni R, Bussolati S, Aldigeri R, Grolli S, Bertini S, Quintavalla F. Evaluation of oxidative stress parameters in healthy saddle horses in relation to housing conditions, presence of stereotypies, age, sex and breed. Processes. 2020;8(12):1670. https://doi.org/10.3390/pr8121670 .
doi: 10.3390/pr8121670
Iemmi T, Menozzi A, Basini G, Grasselli F, Grolli S, Ramoni R, Serventi P, Quintavalla F, Bertini S. Evaluation of oxidative stress in blood of hens (Gallus gallus Domesticus) and magpies (Pica pica) as a tool for the detection of health problems and the assessment of animal welfare. J Avian Med Surg. 2021;35(1):28–36. https://doi.org/10.1647/1082-6742-35.1.28 .
doi: 10.1647/1082-6742-35.1.28 pubmed: 33892586
Quintavalla F, Basini G, Bussolati S, Carrozzo GG, Inglese A, Ramoni R. Redox status in canine Leishmaniasis. Animals. 2021;11:119. https://doi.org/10.3390/ani11010119 .
doi: 10.3390/ani11010119 pubmed: 33429894 pmcid: 7828002
Woolcock AD, Leisering A, Deshuillers P, Roque-Torres J, Moore GE. Feline urinary F2-isoprostanes measured by enzyme-linked immunoassay and gas chromatography–mass spectroscopy are poorly correlated. J Vet Diagn Invest. 2020;32(5):648–55. https://doi.org/10.1177/1040638720939531 .
doi: 10.1177/1040638720939531 pubmed: 32627704 pmcid: 7488965
Todorova I, Simeonova G, Kyuchukova D, Dinev D, Gadjeva V. Reference values of oxidative stress parameters (MDA, SOD, CAT) in dogs and cats. Comp Clin Path. 2005;13:190–4. https://doi.org/10.1007/s00580-005-0547-5 .
doi: 10.1007/s00580-005-0547-5
Castillo C, Pereira V, Abuelo A, Guimarey R, Garcia-Vaquero M, Benedito JL, Hernàndez J. Preliminary results in the redox balance in healthy cats: influence of age and gender. J Feline Med Surg. 2012;15(4):328–32.
doi: 10.1177/1098612X12467996 pubmed: 23172698
Trepanier LA. Antioxidant deficiencies in hospitalized dogs and cats [State of the Art Lecture]. In Proceeding of the World Small Animal Veterinary Association 33° World Congress - Dublin, Ireland, 24–28 august 2008 URL: https://www.vin.com/doc/?id=3866716 .
Keegan RF, Webb CB. Oxidative stress and neutrophil function in cats with chronic renal failure. J Vet Intern Med. 2010;24:514–9.
doi: 10.1111/j.1939-1676.2010.0498.x pubmed: 20384951
Nishi R, Harada A, Hori K, Maeda S, Momoi Y, Yonezawa T. 8-Hydroxy-2’-deoxyguanosine and malondialdeyde in plasma and their association with disease severity in 20 cats with chronic kidney disease. J Feline Med Surg. 2023;25(6):1–7. https://doi.org/10.1177/1098612X23117 .
doi: 10.1177/1098612X23117
Kayar A, Dokuzeylül B, Kandemir FM, Kirbaş A, Bayrakal A, Or ME. Total oxidant and antioxidant capacities, nitric oxide and malondialdehyde levels in cats seropositive for the feline coronavirus. Vet Med. 2015;60(5):274–81. https://doi.org/10.17221/8180-VETMED .
doi: 10.17221/8180-VETMED
Tecles F, Caldin M, Tvarijonaviciute A, Escribano D, Martinez-Subiela S, Ceron JJ. Serum biomarkers of oxidative stress in cats with feline infectious peritonitis. Res Vet Sci. 2015;100:12–7.
doi: 10.1016/j.rvsc.2015.02.007 pubmed: 25819115 pmcid: 7111829
Webb C, Lehman T, McCord K, Avery P, Dow S. Oxidative stress during acute FIV infection in cats. Vet Immunol Immunopathol. 2008;122:16–24.
doi: 10.1016/j.vetimm.2007.11.004 pubmed: 18079001
Webb CB, Falkowski L. Oxidative stress and innate immunity in feline patients with diabetes mellitus: the role of nutrition. J Feline Med Surg. 2009;11:271–6. https://doi.org/10.1016/j.jfms.2008.07.004 .
doi: 10.1016/j.jfms.2008.07.004 pubmed: 18783975
Candellone A, Gianella P, Ceccarelli L, Raviri G, Badino P, Roncone S, Kooistra HS, Meineri G. Redox unbalance in the hyperthyroid cat: a comparison with healthy and non-thyroidal diseased cats. BMC Vet Res. 2019;15:136.
doi: 10.1186/s12917-019-1896-7 pubmed: 31068181 pmcid: 6505105
Whitehouse W, Quimby J, Wan S, Monaghan K, Robbins R, Trepanier LA. Urinary F
doi: 10.1111/jvim.14634 pubmed: 28160524 pmcid: 5354001
Granick M, Leuin AS, Trepanier LA. Plasma and urinary F
doi: 10.1177/1098612X20969358 pubmed: 33146574
Xu Z, Elrashidy RA, Li B, Liu G. Oxidative stress: a putative link between lower urinary tract symptoms and aging and Major Chronic diseases. Front Med (Lausanne). 2022;9:812967. https://doi.org/10.3389/fmed.2022.812967 .
doi: 10.3389/fmed.2022.812967 pubmed: 35360727
Birder LA, Wolf-Johnston A, Buffington CA, Roppolo JR, de Groat WC, Kanai AJ. Altered inducible nitric oxide synthase expression and nitric oxide production in the bladder of cats with feline interstitial cystitis. J Urol. 2005;173:625–9.
doi: 10.1097/01.ju.0000145900.22849.1d pubmed: 15643277
Gerber B, Boretti FS, Kley S, Laluha P, Müller C, Sieber N, Unterer S, Wenger M, Flückiger M, Glaus T, Reusch CE. Evaluation of clinical signs and causes of lower urinary tract disease in European cats. J Small Anim Pract. 2005;46:571–7.
doi: 10.1111/j.1748-5827.2005.tb00288.x pubmed: 16355731
Cooper ES, Lasley E, Daniels JB, Chew DJ. Incidence of bacteriuria at presentation and resulting from urinary catheterization in feline urethral obstruction. J Vet Emerg Crit Care. 2019;29:472–7. https://doi.org/10.1111/vec.12870 .
doi: 10.1111/vec.12870
Beeston D, Humm K, Church DB, Brodbelt D, O’Neill DG. Occurrence and clinical management of urethral obstruction in male cats under primary veterinary care in the United Kingdom in 2016. J Vet Intern Med. 2022;36:599–608. https://doi.org/10.1111/jvim.16389 .
doi: 10.1111/jvim.16389 pubmed: 35199370 pmcid: 8965234
Mauro KD, Bradley CW, Drobatz KJ. Postmortem urinary tract changes in cats with urethral obstruction. J Vet Emerg Crit Care. 2020;30:187–93. https://doi.org/10.1111/vec.12924 .
doi: 10.1111/vec.12924
Krogh HV, Kristensen SA. Study of skin diseases in dogs and cats II. Microflora of the normal skin of dogs and cats. Nord Vet Med. 1976;28:459–63.
pubmed: 980697
Zeeshan M, Aziz T, Naqvi F. Recurrent urinary tract infection by Burkholderia cepacia in a live related renal transplant recipient. J Pak Med Ass. 2012;62(5):496–8.
Lee KW, Lee ST, Cho HC. Burkholderia cepacia causing nosocomial urinary tract infection in children. Child Kidney Dis. 2015;19:143–7.
doi: 10.3339/chikd.2015.19.2.143
Lin ATL, Yang CH, Chen KK, Chang LS. Detrusor mitochondrial lipid peroxidation and superoxide dismutase activity in partial bladder outlet obstruction of rabbits. Neurourol Urodyn. 2005;24:282–7. https://doi.org/10.1002/nau.20109 .
doi: 10.1002/nau.20109 pubmed: 15791627
Dorsch R, Teichmann-Knorrn S, Lund HS. Urinary tract infection and subclinical bacteriuria in cats. A clinical update. J Feline Med Surg. 2019;21:1023–38. https://doi.org/10.1177/1098612X19880435 .
doi: 10.1177/1098612X19880435 pubmed: 31601143 pmcid: 6826873
Creech R, Badri D, Panickar K. Flt3L, a cytokine and growth factor, is reduced in the urine of felines with interstitial cystitis. Curr Dev Nutr. 2021;5(2):1125. https://doi.org/10.1093/cdn/nzab061_009 .
doi: 10.1093/cdn/nzab061_009 pmcid: 8181004
Miyata Y, Matsuo T, Mitsunari K, Asai A, Ohba K, Sakai H. A review of oxidative stress and urinary dysfunction caused by bladder outlet obstruction and treatments using antioxidants. Antioxidants. 2019;8:132. https://doi.org/10.3390/antiox8050132 .
doi: 10.3390/antiox8050132 pubmed: 31096597 pmcid: 6562423
Logadottir YR, Ehren I, Fall M, Wiklund NP, Peeker R. Intravesical nitric oxide production discriminates between classic and nonulcer interstitial cystitis. J Urol. 2004;171:1148–50. https://doi.org/10.1097/01.ju.0000110501.96416.40 .
doi: 10.1097/01.ju.0000110501.96416.40 pubmed: 14767289
Feng Q, Yu X, Qiao Y, Pan S, Wang R, Zheng B, Wang H, Ren K-D, Liu H, Yang Y. Ferroptosis and acute kidney Injury (AKI): Molecular mechanisms and therapeutic potentials. Front Pharmacol. 2022;13:858676. https://doi.org/10.3389/fphar.2022.85867 .
doi: 10.3389/fphar.2022.85867 pubmed: 35517803 pmcid: 9061968
Buffington CA, Pacak K. Increased plasma norepinephrine concentration in cats with interstitial cystitis. J Urol. 2001;165:2051–4.
doi: 10.1016/S0022-5347(05)66292-1 pubmed: 11371926
Radu F, Bean H, Schuler C, Leggett RE, Levin RM. Comparative Evaluation of Antioxidant Reactivity between Ovariectomized and Control Urinary Bladder Tissue Using Ferric Reducing Ability of Plasma and Cupric Ion Reducing Antioxidant Capacity Assays. LUTS. 2009;1(2):93–97. https://doi.org/10.1111/j.1757-5672.2009.00052.x .
Carney HC, Sadek TP, Curtis TM, Halls V, Health S, Hutchison P, Mundschenk K, Westropp JL. AAFP and ISFM guidelines for diagnosing and solving House-Soiling Behavior in cats. J Feline Med Surg. 2014;16:579–98.
doi: 10.1177/1098612X14539092 pubmed: 24966283
Quimby J, Gowland S, Carney HC, DePorter T, Plummer P, Westropp J. 2021 AAHA/AAFP feline life stage guidelines. J Feline Med Surg. 2021;23:211–33.
doi: 10.1177/1098612X21993657 pubmed: 33627003
Markey B, Leonard F, Archambault M, Cullinane A, Maguire D. Clinical veterinary microbiology e-book. Second edition. Elsevier Health Sciences. 2013.

Auteurs

Fausto Quintavalla (F)

Department of Veterinary Sciences, University of Parma, Via del Taglio 10, Parma, 43126, Italy.

Giuseppina Basini (G)

Department of Veterinary Sciences, University of Parma, Via del Taglio 10, Parma, 43126, Italy.

Francesca Fidanzio (F)

Department of Veterinary Sciences, University of Parma, Via del Taglio 10, Parma, 43126, Italy.

Simona Bussolati (S)

Department of Veterinary Sciences, University of Parma, Via del Taglio 10, Parma, 43126, Italy.

Maria Chiara Sabetti (MC)

Department of Veterinary Sciences, University of Parma, Via del Taglio 10, Parma, 43126, Italy.

Maria Cristina Crosta (MC)

Clinica Veterinaria Gran Sasso of Milan, Milan, Italy.

Stefano Grolli (S)

Department of Veterinary Sciences, University of Parma, Via del Taglio 10, Parma, 43126, Italy.

Roberto Ramoni (R)

Department of Veterinary Sciences, University of Parma, Via del Taglio 10, Parma, 43126, Italy. roberto.ramoni@unipr.it.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH