Peer-reviewed veterinary case report
Electrolyte transport problems in dogs with chronic inflammatory
By Dengler, Franziska et al.·Published in Frontiers in veterinary science·2023·Institute of Physiology·View original on PubMed →
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Original publication title: Dysregulation of intestinal epithelial electrolyte transport in canine chronic inflammatory enteropathy and the role of the renin-angiotensin-aldosterone-system.
- Species:
- dog
Plain-English summary
A 5-year-old dog with chronic diarrhea was diagnosed with canine chronic inflammatory enteropathy (CIE), a condition that can lead to significant fluid and electrolyte loss. Researchers found that certain hormones involved in regulating electrolytes were higher in these dogs compared to healthy ones, indicating a potential imbalance. They also discovered that specific electrolyte transporters in the intestines were altered in dogs with CIE. This suggests that treatments aimed at improving electrolyte absorption in the intestines could help manage the condition.
People also search for: dog chronic diarrhea treatment · canine inflammatory bowel disease · electrolyte imbalance in dogs
Abstract
Chronic diarrhea is a hallmark sign of canine chronic inflammatory enteropathy (CIE), leading to fluid and electrolyte losses. Electrolyte homeostasis is regulated by the renin-angiotensin-aldosterone-system (RAAS), which might be involved in (counter-)regulating electrolyte losses in canine CIE. Whether and which electrolyte transporters are affected or if RAAS is activated in canine CIE is unknown. Thus, intestinal electrolyte transporters and components of the RAAS were investigated in dogs with CIE. Serum RAAS fingerprint analysis by mass spectrometry was performed in 5 CIE dogs and 5 healthy controls, and mRNA levels of intestinal electrolyte transporters and local RAAS pathway components were quantified by RT-qPCR in tissue biopsies from the ileum (7 CIE, 10 controls) and colon (6 CIE, 12 controls). Concentrations of RAAS components and mRNA expression of electrolyte transporters were compared between both groups of dogs and were tested for associations among each other. In dogs with CIE, associations with clinical variables were also tested. Components of traditional and alternative RAAS pathways were higher in dogs with CIE than in healthy controls, with statistical significance for Ang I, Ang II, and Ang 1-7 (all < 0.05). Expression of ileal, but not colonic electrolyte transporters, such as Na/K-ATPase, Na/H-exchanger 3, Clchannel 2, down-regulated in adenoma, and Na-glucose-cotransporter (all < 0.05) was increased in CIE. Our results suggest that the dys- or counter-regulation of intestinal electrolyte transporters in canine CIE might be associated with a local influence of RAAS. Activating colonic absorptive reserve capacities may be a promising therapeutic target in canine CIE.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/37720474/