TY - JOUR
T1 - Plasma renin activity and aldosterone concentration in dogs with acquired portosystemic collaterals
AU - Sakamoto, Yumi
AU - Sakai, Manabu
AU - Sato, Keita
AU - Watari, Toshihiro
N1 - Publisher Copyright:
© 2019 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Background: The renin-angiotensin-aldosterone system (RAAS) is activated in humans with portal hypertension (PH) associated with liver disease. However, involvement of RAAS in dogs with intrahepatic PH is not clear. Objective: To measure plasma renin activity (PRA) and plasma aldosterone concentration (PAC) in dogs with PH (chronic hepatitis [CH] and primary hypoplasia of the portal vein [PHPV]), dogs with extrahepatic congenital portosystemic shunt (EH-CPSS), and healthy dogs and to determine whether the RAAS is activated in dogs with PH. Animals: Twenty-seven dogs with acquired portosystemic collaterals (APSCs; 15 dogs with CH, 12 dogs with PHPV), 9 dogs with EH-CPSS, and 10 healthy dogs. Methods: Retrospective study. Plasma renin activity and PAC were measured by radioimmunoassay. Results: Plasma renin activity was significantly higher in the CH group (median, 4.4 ng/mL/h) than in the EH-CPSS (median, 1.0 ng/mL/h; P <.01) and the healthy (median, 1.1 ng/mL/h; P <.01) groups. No significant differences were found between the PHPV group (median, 2.2 ng/mL/h) and other groups. Plasma aldosterone concentration was significantly higher in the CH (median, 111.0 pg/mL) and PHPV (median, 89.5 pg/mL) groups than in the EH-CPSS (median, 1.0 pg/mL; P <.001, P <.01, respectively) and healthy (median, 14.5 pg/mL; P <.001, P <.05, respectively) groups. Conclusions and Clinical Importance: Activation of the RAAS contributes to the pathophysiology of intrahepatic PH in dogs, suggesting that spironolactone may not only be effective for the treatment of ascites but also for the suppression of intrahepatic PH.
AB - Background: The renin-angiotensin-aldosterone system (RAAS) is activated in humans with portal hypertension (PH) associated with liver disease. However, involvement of RAAS in dogs with intrahepatic PH is not clear. Objective: To measure plasma renin activity (PRA) and plasma aldosterone concentration (PAC) in dogs with PH (chronic hepatitis [CH] and primary hypoplasia of the portal vein [PHPV]), dogs with extrahepatic congenital portosystemic shunt (EH-CPSS), and healthy dogs and to determine whether the RAAS is activated in dogs with PH. Animals: Twenty-seven dogs with acquired portosystemic collaterals (APSCs; 15 dogs with CH, 12 dogs with PHPV), 9 dogs with EH-CPSS, and 10 healthy dogs. Methods: Retrospective study. Plasma renin activity and PAC were measured by radioimmunoassay. Results: Plasma renin activity was significantly higher in the CH group (median, 4.4 ng/mL/h) than in the EH-CPSS (median, 1.0 ng/mL/h; P <.01) and the healthy (median, 1.1 ng/mL/h; P <.01) groups. No significant differences were found between the PHPV group (median, 2.2 ng/mL/h) and other groups. Plasma aldosterone concentration was significantly higher in the CH (median, 111.0 pg/mL) and PHPV (median, 89.5 pg/mL) groups than in the EH-CPSS (median, 1.0 pg/mL; P <.001, P <.01, respectively) and healthy (median, 14.5 pg/mL; P <.001, P <.05, respectively) groups. Conclusions and Clinical Importance: Activation of the RAAS contributes to the pathophysiology of intrahepatic PH in dogs, suggesting that spironolactone may not only be effective for the treatment of ascites but also for the suppression of intrahepatic PH.
KW - canine
KW - chronic hepatitis
KW - portal hypertension
KW - primary hypoplasia of the portal vein
KW - renin-angiotensin-aldosterone system
UR - http://www.scopus.com/inward/record.url?scp=85075454504&partnerID=8YFLogxK
U2 - 10.1111/jvim.15661
DO - 10.1111/jvim.15661
M3 - Article
C2 - 31729111
AN - SCOPUS:85075454504
SN - 0891-6640
VL - 34
SP - 139
EP - 144
JO - Journal of Veterinary Internal Medicine
JF - Journal of Veterinary Internal Medicine
IS - 1
ER -