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Liver atrophy and encephalopathy after portacaval shunt in the rat.
Eur Surg Res. 1982; 14(3):192-202.ES

Abstract

The effect of various types of portal diversion (portacaval, mesocaval and pancreatico-splenocaval anastomoses, portacaval transposition and arterialization) on liver atrophy and post-shunt encephalopathy was studied in the rat. Among all diversions, only portacaval anastomosis produced dramatic liver atrophy and encephalopathy. Moreover, portacaval anastomosis was also the only portal diversion which induced low body weight gain. There was no correlation between blood ammonia levels and encephalopathy. Liver atrophy was always correlated to a decrease of hepatic blood flow. Diminution of liver blood flow was only slight following partial (either mesenteric or pancreatico-splenic) diversion of portal blood and nil after portacaval transposition or anastomosis. These results suggest that: (1) pancreatic (insulin-rich) blood is not essential for maintenance of liver trophicity. Hemodynamic factors seem to be predominant in the pathogenesis of post-shunt liver atrophy. (2) Post-shunt encephalopathy arises only when total diversion of the portal blood and liver atrophy are associated.

Authors

No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

7117325

Citation

Castaing, D, et al. "Liver Atrophy and Encephalopathy After Portacaval Shunt in the Rat." European Surgical Research. Europaische Chirurgische Forschung. Recherches Chirurgicales Europeennes, vol. 14, no. 3, 1982, pp. 192-202.
Castaing D, Beaubernard C, Ariogul O, et al. Liver atrophy and encephalopathy after portacaval shunt in the rat. Eur Surg Res. 1982;14(3):192-202.
Castaing, D., Beaubernard, C., Ariogul, O., Gigou, M., Franco, D., & Bismuth, H. (1982). Liver atrophy and encephalopathy after portacaval shunt in the rat. European Surgical Research. Europaische Chirurgische Forschung. Recherches Chirurgicales Europeennes, 14(3), 192-202.
Castaing D, et al. Liver Atrophy and Encephalopathy After Portacaval Shunt in the Rat. Eur Surg Res. 1982;14(3):192-202. PubMed PMID: 7117325.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Liver atrophy and encephalopathy after portacaval shunt in the rat. AU - Castaing,D, AU - Beaubernard,C, AU - Ariogul,O, AU - Gigou,M, AU - Franco,D, AU - Bismuth,H, PY - 1982/1/1/pubmed PY - 1982/1/1/medline PY - 1982/1/1/entrez SP - 192 EP - 202 JF - European surgical research. Europaische chirurgische Forschung. Recherches chirurgicales europeennes JO - Eur Surg Res VL - 14 IS - 3 N2 - The effect of various types of portal diversion (portacaval, mesocaval and pancreatico-splenocaval anastomoses, portacaval transposition and arterialization) on liver atrophy and post-shunt encephalopathy was studied in the rat. Among all diversions, only portacaval anastomosis produced dramatic liver atrophy and encephalopathy. Moreover, portacaval anastomosis was also the only portal diversion which induced low body weight gain. There was no correlation between blood ammonia levels and encephalopathy. Liver atrophy was always correlated to a decrease of hepatic blood flow. Diminution of liver blood flow was only slight following partial (either mesenteric or pancreatico-splenic) diversion of portal blood and nil after portacaval transposition or anastomosis. These results suggest that: (1) pancreatic (insulin-rich) blood is not essential for maintenance of liver trophicity. Hemodynamic factors seem to be predominant in the pathogenesis of post-shunt liver atrophy. (2) Post-shunt encephalopathy arises only when total diversion of the portal blood and liver atrophy are associated. SN - 0014-312X UR - https://www.unboundmedicine.com/medline/citation/7117325/Liver_atrophy_and_encephalopathy_after_portacaval_shunt_in_the_rat_ L2 - https://www.karger.com?DOI=10.1159/000128289 DB - PRIME DP - Unbound Medicine ER -