## Abstract Liver tumors, both primary and secondary, receive their main blood supply from the hepatic artery. Hepatic artery ligation (HAL) causes a reduction in tumor growth and tumor necrosis. In this experiment, three different experimental tumors were used to study the effect of hepatic artery
The influence of hepatic artery ligation and of vasopressin on liver tumour blood flow in rats
✍ Scribed by Peter Naredi; Per Lindér; Stig B. Holmberg; Rigmor Söderberg; Göran Carlsson; Bengt Gustavsson; Lars Jacobsson; Dr. Larsolof Hafström
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 585 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0022-4790
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The blood flow in an experimental adenocarcinoma in the rat liver was determined with the ^133^Xe‐washout technique before and after hepatic artery ligation (HAL). There was an initial reduction of the washout of 50%. This was further reduced after 1 day by 50%, which was maintained for 7 days. Seven days after HAL or sham procedures the ^133^Xe‐washout was of similar magnitude in the liver tumours, although after the sham procedure the tumours were larger (3.4 g vs. 1.5 g). The estimated tumour blood flow was then approximately 0.04 ml × min^−1^ × g^−1^. The influence on normal liver parenchyma of HAL was a reduction at 30 minutes, which was maintained for 7 days. Postacton®—a synthetic vasopressin—did not influence the ^133^Xe‐washout in normal liver parenchyma in non‐tumour, as well as in tumour‐bearing animals. There was no influence of Postacton® on the ^133^Xe‐washout in the liver tumours. Thirty minutes after HAL Postacton® gave a reduction of blood flow in normal liver parenchyma of tumour‐bearing animals, which is thus only from the portal vein. In tumours Postacton® did not significantly reduce the tumour blood flow immediately after HAL. © 1992 Wiley‐Liss, Inc.
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