Chang Tung-Huei, Hakamada Kenichi, Toyoki Yoshikazu, Tsuchida Shigeki, Sasaki Mutsuo
Second Department of Surgery, Hirosaki University School of Medicine, Hirosaki, Japan.
Transplantation. 2004 Jan 15;77(1):22-7. doi: 10.1097/01.TP.0000089234.93366.6D.
Small-for-size grafts often cause persistent conjugated hyperbilirubinemia in the recipient after adult-to-adult living donor liver transplantation, but the cause has not yet been clarified. In physiologic status, bilirubin is excreted from hepatocytes to the bile canaliculus by means of multidrug resistance protein (MRP) 2 and, in particular circumstances, by means of MRP3 to the sinusoidal space. The aim of this study was to research whether there is any change in bilirubin excretion pattern during liver regeneration with reference to expression of MRP2 and MRP3.
Sprague-Dawley rats underwent sham operation (n=37), 70% hepatectomy (n=38), or 90% hepatectomy (n=37). The degree of liver regeneration, total and direct bilirubin, protein synthesis, and interleukin (IL)-6 were serially assessed. Expression of MRP2 and MRP3 were semiquantified by Western blotting.
The proliferating cell nuclear antigen labeling index indicated rapid liver regeneration after 70% and 90% hepatectomy. Serum levels of total and direct bilirubin increased significantly (P<0.05), and conjugated hyperbilirubinemia was proved only in the 90% hepatectomy group. Coagulation factor VII dipped but increased as early as 12 to 24 hr postoperatively in both hepatectomy groups. Plasma IL-6 levels were significantly increased in the 90% hepatectomy group (P<0.05). Expression of MRP2 was decreased and MRP3 was expressed at 36 and 72 hr postoperatively in the 90% hepatectomy group, whereas no change was observed in MRP expression in the 70% hepatectomy group.
During liver regeneration after critical hepatectomy such as 90% hepatectomy, decrease of MRP2 and expression of MRP3 may play an important role in postoperative hyperbilirubinemia.
在成人活体肝移植术后,小体积供肝常导致受者出现持续性结合胆红素血症,但其病因尚未明确。在生理状态下,胆红素通过多药耐药蛋白(MRP)2从肝细胞排泄至胆小管,在特定情况下,通过MRP3排泄至窦状隙。本研究旨在探讨肝再生过程中胆红素排泄模式是否会因MRP2和MRP3的表达而发生变化。
将Sprague-Dawley大鼠分为假手术组(n = 37)、70%肝切除组(n = 38)或90%肝切除组(n = 37)。连续评估肝再生程度、总胆红素和直接胆红素、蛋白质合成以及白细胞介素(IL)-6水平。通过蛋白质印迹法对MRP2和MRP3的表达进行半定量分析。
增殖细胞核抗原标记指数表明,70%和90%肝切除术后肝再生迅速。总胆红素和直接胆红素的血清水平显著升高(P < 0.05),且仅在90%肝切除组证实存在结合胆红素血症。两个肝切除组的凝血因子VII均下降,但在术后12至24小时即开始升高。90%肝切除组的血浆IL-6水平显著升高(P < 0.05)。90%肝切除组术后36小时和72小时MRP2表达降低,MRP3表达,而70%肝切除组的MRP表达未见变化。
在90%肝切除等严重肝切除术后的肝再生过程中,MRP2的减少和MRP3的表达可能在术后高胆红素血症中起重要作用。