Vasoactive intestinal peptide in canine portosystemic shunt in the absence of portal hypertension

Background: The congenital portosystemic shunt (PSS) is a common vascular anomaly in dogs. Vasoactive intestinal peptide (VIP) is produced in various organs (including the small intestine, large intestine, and pancreas), leading to abdominal vasodilation, increased blood flow, increased pancreatic b...

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Main Authors: Mitsuhiro Isaka, Hiroshi Ueno
Format: Article
Language:English
Published: Tripoli University 2021-01-01
Series:Open Veterinary Journal
Subjects:
Online Access:https://www.openveterinaryjournal.com/OVJ-2020-11-323%20M.%20Isaka%20and%20H.%20Ueno.pdf
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author Mitsuhiro Isaka
Hiroshi Ueno
author_facet Mitsuhiro Isaka
Hiroshi Ueno
author_sort Mitsuhiro Isaka
collection DOAJ
description Background: The congenital portosystemic shunt (PSS) is a common vascular anomaly in dogs. Vasoactive intestinal peptide (VIP) is produced in various organs (including the small intestine, large intestine, and pancreas), leading to abdominal vasodilation, increased blood flow, increased pancreatic blood flow, and promotion of pancreatic endocrine and exocrine secretion. However, there have been no reports on the concentration of VIP in the portal and peripheral veins in canine PSS. Aim: The aim of this pilot study was to evaluate whether dogs with PSS have a different VIP concentration in their portal system in general. Methods: Six dogs with an extrahepatic portosplenic shunt were included in the study. Blood samples were taken from the saphenous and portal vein during PSS ligation surgery with an amerid constrictor, to evaluate and compare the VIP concentration in both samples. VIP was measured using a commercial canine enzyme-linked immunosorbent assay kit. Results: The breeds included Mongrels (n = 2), Norfolk Terriers (n = 1), Miniature Dachshunds (n = 1), and Maltese (n = 2), and their ages were 9.3 ± 6.5 months; the bodyweight was 3.3 ± 0.8 kg. The concentration of VIP in the saphenous vein was 17.75 ± 13.88 pg/mL; in contrast, the concentration of VIP in the portal vein was 29.7 ± 20.29 pg/mL. There was no significant difference in the VIP concentration between veins. Conclusion: There was no difference in the VIP concentration between the portal and saphenous veins, suggesting non-association between VIP and the PSS, in the absence of portal hypertension.
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spelling doaj.art-8ddf04d8b0a34a50afdf58e9ae37cd8f2022-12-21T20:12:24ZengTripoli UniversityOpen Veterinary Journal2218-60502218-60502021-01-011113941http://dx.doi.org/10.4314/ovj.v11i1.7Vasoactive intestinal peptide in canine portosystemic shunt in the absence of portal hypertensionMitsuhiro Isaka0Hiroshi Ueno1Department of Small Animal Clinical Sciences, School of Veterinary Medicine, Rakuno Gakuen University, 582 Bunkyodai-Midorimachi, Ebetsu, Hokkaido 069-8501, JapanDepartment of Small Animal Clinical Sciences, School of Veterinary Medicine, Rakuno Gakuen University, 582 Bunkyodai-Midorimachi, Ebetsu, Hokkaido 069-8501, JapanBackground: The congenital portosystemic shunt (PSS) is a common vascular anomaly in dogs. Vasoactive intestinal peptide (VIP) is produced in various organs (including the small intestine, large intestine, and pancreas), leading to abdominal vasodilation, increased blood flow, increased pancreatic blood flow, and promotion of pancreatic endocrine and exocrine secretion. However, there have been no reports on the concentration of VIP in the portal and peripheral veins in canine PSS. Aim: The aim of this pilot study was to evaluate whether dogs with PSS have a different VIP concentration in their portal system in general. Methods: Six dogs with an extrahepatic portosplenic shunt were included in the study. Blood samples were taken from the saphenous and portal vein during PSS ligation surgery with an amerid constrictor, to evaluate and compare the VIP concentration in both samples. VIP was measured using a commercial canine enzyme-linked immunosorbent assay kit. Results: The breeds included Mongrels (n = 2), Norfolk Terriers (n = 1), Miniature Dachshunds (n = 1), and Maltese (n = 2), and their ages were 9.3 ± 6.5 months; the bodyweight was 3.3 ± 0.8 kg. The concentration of VIP in the saphenous vein was 17.75 ± 13.88 pg/mL; in contrast, the concentration of VIP in the portal vein was 29.7 ± 20.29 pg/mL. There was no significant difference in the VIP concentration between veins. Conclusion: There was no difference in the VIP concentration between the portal and saphenous veins, suggesting non-association between VIP and the PSS, in the absence of portal hypertension.https://www.openveterinaryjournal.com/OVJ-2020-11-323%20M.%20Isaka%20and%20H.%20Ueno.pdfdogsportosystemic shuntvasoactive intestinal peptide
spellingShingle Mitsuhiro Isaka
Hiroshi Ueno
Vasoactive intestinal peptide in canine portosystemic shunt in the absence of portal hypertension
Open Veterinary Journal
dogs
portosystemic shunt
vasoactive intestinal peptide
title Vasoactive intestinal peptide in canine portosystemic shunt in the absence of portal hypertension
title_full Vasoactive intestinal peptide in canine portosystemic shunt in the absence of portal hypertension
title_fullStr Vasoactive intestinal peptide in canine portosystemic shunt in the absence of portal hypertension
title_full_unstemmed Vasoactive intestinal peptide in canine portosystemic shunt in the absence of portal hypertension
title_short Vasoactive intestinal peptide in canine portosystemic shunt in the absence of portal hypertension
title_sort vasoactive intestinal peptide in canine portosystemic shunt in the absence of portal hypertension
topic dogs
portosystemic shunt
vasoactive intestinal peptide
url https://www.openveterinaryjournal.com/OVJ-2020-11-323%20M.%20Isaka%20and%20H.%20Ueno.pdf
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