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An Imaging and Histological Study on Intrahepatic Microvascular Passage of Contrast Materials in Rat Liver
Background. Lipiodol has been applied for decades in transarterial chemoembolization to treat liver malignancies, but its intrahepatic pathway through arterioportal shunt (APS) in the liver has not been histologically revealed. This rodent experiment was conducted to provide evidence for the pathway...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331418/ https://www.ncbi.nlm.nih.gov/pubmed/28293625 http://dx.doi.org/10.1155/2017/1419545 |
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author | Xia, Qian Feng, Yuanbo Yin, Ting Liu, Yewei Zhang, Guozhi Liu, Jianjun Tong, Linjun Willemyns, Robin Yu, Jie Oyen, Raymond Huang, Gang Ni, Yicheng |
author_facet | Xia, Qian Feng, Yuanbo Yin, Ting Liu, Yewei Zhang, Guozhi Liu, Jianjun Tong, Linjun Willemyns, Robin Yu, Jie Oyen, Raymond Huang, Gang Ni, Yicheng |
author_sort | Xia, Qian |
collection | PubMed |
description | Background. Lipiodol has been applied for decades in transarterial chemoembolization to treat liver malignancies, but its intrahepatic pathway through arterioportal shunt (APS) in the liver has not been histologically revealed. This rodent experiment was conducted to provide evidence for the pathway of Lipiodol delivered through the hepatic artery (HA) but found in the portal vein (PV) and to elucidate the observed unidirectional APS. Methods. Thirty rats were divided into 5 groups receiving systemic or local arterial infusion of red-stained iodized oil (RIO) or its hydrosoluble substitute barium sulfate suspension (BSS), or infusion of BSS via the PV, monitored by real-time digital radiography. Histomorphology of serial frozen and paraffin sections was performed and quantified. Results. After HA infusion, RIO and BSS appeared extensively in PV lumens with peribiliary vascular plexus (PVP) identified as the responsible anastomotic channel. After PV infusion, BSS appeared predominantly in the PV and surrounding sinusoids and to a much lesser extent in the PVP and HA (P < 0.001). Fluid mechanics well explains the one-way-valve phenomenon of APS. Conclusions. Intravascularly injected rat livers provide histomorphologic evidences: (1) the PVP exists in between the HA and PV, which is responsible to the APS of Lipiodol; and (2) the intrahepatic vascular inflow appears HA-PVP-PV unidirectional without a physical one-way valve, which can be postulated by the fluid mechanics. |
format | Online Article Text |
id | pubmed-5331418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-53314182017-03-14 An Imaging and Histological Study on Intrahepatic Microvascular Passage of Contrast Materials in Rat Liver Xia, Qian Feng, Yuanbo Yin, Ting Liu, Yewei Zhang, Guozhi Liu, Jianjun Tong, Linjun Willemyns, Robin Yu, Jie Oyen, Raymond Huang, Gang Ni, Yicheng Biomed Res Int Research Article Background. Lipiodol has been applied for decades in transarterial chemoembolization to treat liver malignancies, but its intrahepatic pathway through arterioportal shunt (APS) in the liver has not been histologically revealed. This rodent experiment was conducted to provide evidence for the pathway of Lipiodol delivered through the hepatic artery (HA) but found in the portal vein (PV) and to elucidate the observed unidirectional APS. Methods. Thirty rats were divided into 5 groups receiving systemic or local arterial infusion of red-stained iodized oil (RIO) or its hydrosoluble substitute barium sulfate suspension (BSS), or infusion of BSS via the PV, monitored by real-time digital radiography. Histomorphology of serial frozen and paraffin sections was performed and quantified. Results. After HA infusion, RIO and BSS appeared extensively in PV lumens with peribiliary vascular plexus (PVP) identified as the responsible anastomotic channel. After PV infusion, BSS appeared predominantly in the PV and surrounding sinusoids and to a much lesser extent in the PVP and HA (P < 0.001). Fluid mechanics well explains the one-way-valve phenomenon of APS. Conclusions. Intravascularly injected rat livers provide histomorphologic evidences: (1) the PVP exists in between the HA and PV, which is responsible to the APS of Lipiodol; and (2) the intrahepatic vascular inflow appears HA-PVP-PV unidirectional without a physical one-way valve, which can be postulated by the fluid mechanics. Hindawi Publishing Corporation 2017 2017-02-15 /pmc/articles/PMC5331418/ /pubmed/28293625 http://dx.doi.org/10.1155/2017/1419545 Text en Copyright © 2017 Qian Xia et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Xia, Qian Feng, Yuanbo Yin, Ting Liu, Yewei Zhang, Guozhi Liu, Jianjun Tong, Linjun Willemyns, Robin Yu, Jie Oyen, Raymond Huang, Gang Ni, Yicheng An Imaging and Histological Study on Intrahepatic Microvascular Passage of Contrast Materials in Rat Liver |
title | An Imaging and Histological Study on Intrahepatic Microvascular Passage of Contrast Materials in Rat Liver |
title_full | An Imaging and Histological Study on Intrahepatic Microvascular Passage of Contrast Materials in Rat Liver |
title_fullStr | An Imaging and Histological Study on Intrahepatic Microvascular Passage of Contrast Materials in Rat Liver |
title_full_unstemmed | An Imaging and Histological Study on Intrahepatic Microvascular Passage of Contrast Materials in Rat Liver |
title_short | An Imaging and Histological Study on Intrahepatic Microvascular Passage of Contrast Materials in Rat Liver |
title_sort | imaging and histological study on intrahepatic microvascular passage of contrast materials in rat liver |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331418/ https://www.ncbi.nlm.nih.gov/pubmed/28293625 http://dx.doi.org/10.1155/2017/1419545 |
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