Serum Proteomic Changes in Dogs with Different Stages of Chronic Heart Failure

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  • Ahmet Saril
  • Meric Kocaturk
  • Kazumi Shimada
  • Akiko Uemura
  • Emel Akgün
  • Pinar Levent
  • Ahmet Tarik Baykal
  • Alberto Muñoz Prieto
  • Carlos Fernando Agudelo
  • Ryou Tanaka
  • Jose Joaquin Ceron
  • Koch, Jørgen
  • Zeki Yilmaz

MMVD, the most common cause of CHF in dogs, is a chronic disease with variable clinical signs, with some patients remaining asymptomatic while others develop CHF. Here, we aimed to evaluate serum proteins by proteomic analysis in dogs at different stages of CHF due to MMVD, and proteome behaviors after conventional treatment. A total of 32 dogs were divided equally into four groups—stage A (healthy/controls), stage B2 (asymptomatic), stage C and stage D (symptomatic)—according to the ACVIM consensus. Serum proteomes were evaluated using LC/MS-based label-free differential proteome analysis. The study revealed 157 different proteins; 11 were up-and 21 down-regulated in dogs with CHF compared to controls. In stage B2 dogs, angiotensinogen (AGT) was up-regulated, but immunoglobulin iota chain-like, lipopolysaccharide-binding protein, and carboxypeptidase (CPN) were down-regulated. In stage C dogs, complement C3 (C3) and inter-alpha-trypsin inhibitor heavy chain were up-regulated, but hemopexin, and actin-cytoplasmic-1 (ACT-1) were down-regulated. In stage D dogs, AGT was up-regulated, whereas tetranectin, paraoxonase-1, adiponectin and ACT-1 were down-regulated. A decrease in CPN, C3 and AGT and an increase in ACT-1 were observed after treatment of dogs in stage C. This pilot study identified that dogs at different stages of CHF show different serum protein composition which has potential to be biomarker for diagnose and treatment monitorization.

OriginalsprogEngelsk
Artikelnummer490
TidsskriftAnimals
Vol/bind12
Udgave nummer4
ISSN2076-2615
DOI
StatusUdgivet - 2022

Bibliografisk note

Funding Information:
Funding: This project was supported by Bursa Uludag University Research Fund [OUAP(V)-2018/12, Bursa, Turkey] for Ph.D. thesis of A. SARIL (first author).

Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.

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