Xia Qian, Feng Yuanbo, Yin Ting, Liu Yewei, Zhang Guozhi, Liu Jianjun, Tong Linjun, Willemyns Robin, Yu Jie, Oyen Raymond, Huang Gang, Ni Yicheng
Department of Nuclear Medicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, 160 Pu Jian Road, Shanghai 200127, China; Department of Imaging and Pathology, University Hospitals, KU Leuven, Herestraat 49, 3000 Leuven, Belgium.
Department of Imaging and Pathology, University Hospitals, KU Leuven, Herestraat 49, 3000 Leuven, Belgium.
Biomed Res Int. 2017;2017:1419545. doi: 10.1155/2017/1419545. Epub 2017 Feb 15.
. 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. . 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. . 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 ( < 0.001). Fluid mechanics well explains the one-way-valve phenomenon of APS. . 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.
碘油已在经动脉化疗栓塞中应用数十年以治疗肝脏恶性肿瘤,但其在肝脏中通过动静脉分流(APS)的肝内途径尚未在组织学上得到揭示。进行这项啮齿动物实验是为了提供证据证明经肝动脉(HA)注入但在门静脉(PV)中发现的碘油的途径,并阐明观察到的单向APS。30只大鼠被分为5组,分别接受全身或局部动脉注射红色碘化油(RIO)或其水溶性替代物硫酸钡混悬液(BSS),或经PV注射BSS,通过实时数字射线摄影进行监测。对连续的冰冻和石蜡切片进行组织形态学分析并定量。HA注射后,RIO和BSS广泛出现在PV管腔中,胆小管周围血管丛(PVP)被确定为负责的吻合通道。经PV注射后,BSS主要出现在PV和周围的肝血窦中,而在PVP和HA中出现的程度要小得多(<0.001)。流体力学很好地解释了APS的单向阀现象。血管内注射大鼠肝脏提供了组织形态学证据:(1)HA和PV之间存在PVP,它是碘油APS的原因;(2)肝内血管流入呈现HA-PVP-PV单向,没有物理单向阀,这可以由流体力学推测得出。