A urinary proteomic study in hypercalciuric dogs with and without calcium oxalate urolithiasis.

calcium oxalate stone dog hypercalciuria urinary biomarker

Journal

Veterinary world
ISSN: 0972-8988
Titre abrégé: Vet World
Pays: India
ID NLM: 101504872

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 08 08 2022
accepted: 04 11 2022
entrez: 31 1 2023
pubmed: 1 2 2023
medline: 1 2 2023
Statut: ppublish

Résumé

Hypercalciuria is an important predisposing factor commonly found in humans and dogs with calcium oxalate (CaOx) urolithiasis. Calcium oxalate crystals can induce an inflammatory reaction that subsequently produces several proteins that have an inhibitory or stimulatory effect on stone formation. This study aimed to evaluate the differences in urinary proteomic profiles between hypercalciuric CaOx stone dogs and hypercalciuric stone-free dogs (CaOx stone and control groups, respectively). Seven dogs with hypercalciuric CaOx urolithiasis and breed-, sex-, and aged-matched controls with hypercalciuria were included in the study. Serum and urine samples were obtained from all dogs to analyze electrolytes. Urinary proteomic profiles were analyzed using liquid chromatography-mass spectrometry. Student's t-test was used to compare the differences between groups. Forty-nine urinary proteins were identified in the stone-free and CaOx stone groups, whereas 19 and 6 proteins were unique in the CaOx stone and stone-free groups, respectively. The urinary thrombomodulin level was significantly higher in the CaOx stone group (relative ratio = 1.8, p < 0.01) than in the stone-free group. This study demonstrated that urinary proteomic profiles may be used as a candidate biomarker for urinary tract injury in CaOx urolithiasis in dogs.

Sections du résumé

Background and Aims UNASSIGNED
Hypercalciuria is an important predisposing factor commonly found in humans and dogs with calcium oxalate (CaOx) urolithiasis. Calcium oxalate crystals can induce an inflammatory reaction that subsequently produces several proteins that have an inhibitory or stimulatory effect on stone formation. This study aimed to evaluate the differences in urinary proteomic profiles between hypercalciuric CaOx stone dogs and hypercalciuric stone-free dogs (CaOx stone and control groups, respectively).
Materials and Methods UNASSIGNED
Seven dogs with hypercalciuric CaOx urolithiasis and breed-, sex-, and aged-matched controls with hypercalciuria were included in the study. Serum and urine samples were obtained from all dogs to analyze electrolytes. Urinary proteomic profiles were analyzed using liquid chromatography-mass spectrometry. Student's t-test was used to compare the differences between groups.
Results UNASSIGNED
Forty-nine urinary proteins were identified in the stone-free and CaOx stone groups, whereas 19 and 6 proteins were unique in the CaOx stone and stone-free groups, respectively. The urinary thrombomodulin level was significantly higher in the CaOx stone group (relative ratio = 1.8, p < 0.01) than in the stone-free group.
Conclusion UNASSIGNED
This study demonstrated that urinary proteomic profiles may be used as a candidate biomarker for urinary tract injury in CaOx urolithiasis in dogs.

Identifiants

pubmed: 36718335
doi: 10.14202/vetworld.2022.2937-2944
pii: Vetworld-15-2937
pmc: PMC9880843
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2937-2944

Informations de copyright

Copyright: © Chamsuwan, et al.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

Références

Appl Biochem Biotechnol. 2009 Oct;159(1):221-32
pubmed: 19145410
Int J Mol Sci. 2019 Feb 19;20(4):
pubmed: 30791405
Circulation. 1997 Nov 4;96(9):2938-43
pubmed: 9386160
Vet Sci. 2022 Jun 09;9(6):
pubmed: 35737335
Res Vet Sci. 2017 Dec;115:366-370
pubmed: 28710955
Clin Sci (Lond). 1991 Oct;81(4):477-81
pubmed: 1682080
J Anim Physiol Anim Nutr (Berl). 2006 Jun;90(5-6):192-9
pubmed: 16684139
Nat Med. 2007 Nov;13(11):1349-58
pubmed: 17982464
PeerJ. 2021 Jul 27;9:e11872
pubmed: 34395096
BMC Nephrol. 2020 Jul 22;21(1):292
pubmed: 32698782
Urology. 2003 Sep;62(3):566-70
pubmed: 12946778
Urolithiasis. 2017 Aug;45(4):329-336
pubmed: 28361470
Am J Physiol Cell Physiol. 2017 Apr 1;312(4):C459-C477
pubmed: 28122734
Arch Intern Med. 2009 Jul 13;169(13):1210-5
pubmed: 19597070
Proteome Sci. 2016 Feb 27;14:4
pubmed: 26924944
J Vet Intern Med. 2015 Jan;29(1):113-9
pubmed: 25581880
Kidney Blood Press Res. 2020;45(3):391-406
pubmed: 32146474
Nat Rev Urol. 2020 Dec;17(12):691-705
pubmed: 33159170
Mol Cell Biol. 2004 Aug;24(16):7214-24
pubmed: 15282320
Biomedicines. 2021 Jul 06;9(7):
pubmed: 34356845
Anal Biochem. 1976 May 7;72:248-54
pubmed: 942051
Am J Vet Res. 2002 Mar;63(3):330-7
pubmed: 11911566
Orphanet J Rare Dis. 2020 Nov 11;15(1):319
pubmed: 33176829
EBioMedicine. 2019 Dec;50:366-378
pubmed: 31735555
Am J Pathol. 2003 Apr;162(4):1241-8
pubmed: 12651616
J Vet Intern Med. 2019 Mar;33(2):758-763
pubmed: 30851134
Physiol Rep. 2021 Jan;9(1):e14658
pubmed: 33403824
Nat Rev Nephrol. 2021 Jun;17(6):417-433
pubmed: 33514941
Prev Vet Med. 2014 Aug 1;115(3-4):217-28
pubmed: 24834804
Toxicology. 2011 Nov 28;290(1):82-8
pubmed: 21907259
JAMA. 2005 Apr 6;293(13):1653-62
pubmed: 15811985
Clin Chim Acta. 2014 Feb 15;429:81-9
pubmed: 24333391
Urolithiasis. 2017 Aug;45(4):337-346
pubmed: 28314883
Vet Clin Pathol. 2014 Jun;43(2):193-205
pubmed: 24773128
J Am Vet Med Assoc. 2016 Dec 1;249(11):1274-1280
pubmed: 27875079
J Small Anim Pract. 2003 Nov;44(11):491-6
pubmed: 14635961
Oxid Med Cell Longev. 2018 Feb 28;2018:1619293
pubmed: 29682152
PLoS One. 2013 Jul 09;8(7):e68624
pubmed: 23874695
Adv Urol. 2018 Feb 4;2018:3068365
pubmed: 29515627
PLoS One. 2017 May 3;12(5):e0176595
pubmed: 28467511
Thromb Haemost. 2012 Dec;108(6):1141-53
pubmed: 23014597
Int J Mol Sci. 2019 Aug 09;20(16):
pubmed: 31404995
J Vet Intern Med. 2020 Mar;34(2):754-760
pubmed: 31926039
J Biol Chem. 2002 May 3;277(18):16332-9
pubmed: 11872745
Int J Mol Med. 2021 Aug;48(2):
pubmed: 34132361
Kidney Int. 2002 May;61(5):1646-54
pubmed: 11967014

Auteurs

Sumonwan Chamsuwan (S)

Department of Physiology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.

Chollada Buranakarl (C)

Department of Physiology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.

Kris Angkanaporn (K)

Department of Physiology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.

Thasinas Dissayabutra (T)

Metabolic Disease in Gut and Urinary System Research Unit, Department of Biochemistry, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Natthaya Chuaypen (N)

Metabolic Disease in Gut and Urinary System Research Unit, Department of Biochemistry, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Trairak Pisitkun (T)

Center of Excellence in Systems Biology, Research Affairs, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Nuttiya Kalpongnukul (N)

Center of Excellence in Systems Biology, Research Affairs, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Classifications MeSH