scholarly journals Triolein emulsion infusion into the hepatic artery increases vascular permeability to doxorubicin in rabbit liver

2021 ◽  
Vol 27 (2) ◽  
pp. 152-161
Author(s):  
Yong-Woo Kim ◽  
Hak Jin Kim ◽  
Byung Mann Cho ◽  
Seon Hee Choi
2006 ◽  
Vol 3 (2) ◽  
pp. 134-137 ◽  
Author(s):  
Hongxin Zhang ◽  
Wei Cao ◽  
Zhimin Wang ◽  
Weiping Guo ◽  
Daihui Ni ◽  
...  

2013 ◽  
Vol 12 (6) ◽  
pp. 622-629 ◽  
Author(s):  
Krijn P van Lienden ◽  
Lisette T Hoekstra ◽  
Jessica D van Trigt ◽  
Joris J Roelofs ◽  
Otto M van Delden ◽  
...  

1990 ◽  
Vol 24 (1) ◽  
pp. 14-24 ◽  
Author(s):  
G. W. Meijer ◽  
M. J. H. Geelen ◽  
H. Van Herck ◽  
J. W. M. A. Mullink ◽  
L. F. M. Van Zutphen ◽  
...  

We describe a method for the isolation and recirculating perfusion of rabbit livers. Livers were perfused simultaneously through the portal vein and the hepatic artery. Precise descriptions of the surgical preparation, perfusion apparatus and perfusion method are given. The viability of rabbit livers was assessed with the use of physiological, biochemical and histological parameters. We conclude that the isolated perfused rabbit livers are sufficiently viable to study their short-term metabolism.


Swiss Surgery ◽  
1999 ◽  
Vol 5 (3) ◽  
pp. 143-146 ◽  
Author(s):  
Launois ◽  
Maddern ◽  
Tay

The detailed knowledge of the segmental anatomy of the liver has led to a rapid evolution in resectional surgery based on the intrahepatic distribution of the portal trinity (the hepatic artery, hepatic duct and portal vein). The classical intrafascial or extrahepatic approach is to isolate the appropriate branch of the portal vein, hepatic artery and the hepatic duct, outside the liver substance. Another method, the extrafascial approach, is to dissect the whole sheath of the pedicle directly after division of a substantial amount of the hepatic tissue to reach the pedicle, which is surrounded by a sheath, derived from Glisson's capsule. This Glissonian sheath encloses the portal trinity. In the transfissural or intrahepatic approach, these sheaths can be approached either anteriorly (after division of the main, right or umbilical fissure) or posteriorly from behind the porta hepatis. We describe the technique for approaching the Glissonian sheath and hence the hepatic pedicle structures and their branches by the intrahepatic posterior approach that allows early delineation of the liver segment without the need for ancillary techniques. In addition, the indications for the use of this technique in the technical and oncologic settings are also discussed.


2002 ◽  
Vol 13 (4) ◽  
pp. 293-304
Author(s):  
Nancy Kemeny ◽  
Matt Galsky

1963 ◽  
Vol 10 (01) ◽  
pp. 071-080 ◽  
Author(s):  
L. B Jaques ◽  
C Mary Jaques

SummaryPreparations were made of rabbit liver globulin by the method of Jaques for heparinase and their effect on heparin studied. The results confirmed the observations of a progressive loss of anticoagulant activity with globulin in 0.9% saline, of a loss of metachromatic activity after phenol extraction and the reversal of the latter by alkali. The latter observations were due to the solubility in phenol of heparin on combination with protein. With suitable preparations, a decrease in anticoagulant activity without decrease in metachromatic activity was observed, i.e. conversion of heparin to uroheparin. Loss of heparin due to combination with protein and resulting precipitation, solubility in phenol, etc. followed a protein pH-dissociation curve. Loss of heparin anticoagulant activity due to heparinase was maximal at pH 5.4. No loss of heparin occurred at pH values more acid than 5 or more alkaline than 7.


2008 ◽  
Vol 58 (4) ◽  
pp. 399
Author(s):  
Eun Soo Kim ◽  
Kyung Mi Jang ◽  
Min Jeong Kim ◽  
Hoi Soo Yoon ◽  
Hyun Lee ◽  
...  

1960 ◽  
Vol XXXIII (IV) ◽  
pp. 532-538 ◽  
Author(s):  
H. Breuer ◽  
Gerta Pangels
Keyword(s):  

ABSTRACT The metabolism of oestrone, oestradiol-17α and oestradiol-17β has been studied in rabbit liver slices. Oestradiol-17α and oestradiol-17β were isolated as metabolites of oestrone. When oestradiol-17α17α was incubated oestrone and oestradiol-17β were formed, whereas oestradiol-17β gave rise to oestradiol-17α and oestrone. Quantitative experiments showed that after incubation of oestrone 5–8 times as much oestradiol-17β was found as oestradiol-17α.


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