Gaeta G B, Utili R, Adinolfi L E, Tripodi M F, Esposito V
Clinica Malattie Infettive, 1st Medical School, University of Naples, Italy.
J Hepatol. 1989 May;8(3):344-50. doi: 10.1016/0168-8278(89)90033-0.
The effects of amphotericin B (AmB) on the hepatic excretory function and the colloid clearance capacity were investigated in the perfused rat liver. AmB at 5 or 10 microM caused dose-dependent reductions in bile and perfusate flow rates and in biliary bile acid (BA) excretion. BA concentration in bile tended to increase, due to a prominent reduction in bile water induced by the drug. At 5 microM, AmB also caused an increase in [14C]sucrose clearance by the liver and a release of hepatocytic enzymes into the perfusate. These alterations were not related to the decrease in the perfusate flow induced by AmB. In addition, the drug, at 5 microM, caused a significant decrease in the colloidal carbon clearance by the liver. In this case also, the effect was independent of the reduction in the perfusate flow induced by the drug. The toxic effects of AmB on the rat liver could be interpreted as a derangement of the cell membrane functional integrity, which causes cholestasis, enzyme leakage and an impairment of the reticuloendothelial system function. This latter effect deserves careful evaluation of its clinical implications.
在灌注大鼠肝脏中研究了两性霉素B(AmB)对肝脏排泄功能和胶体清除能力的影响。5或10微摩尔的AmB导致胆汁和灌注液流速以及胆汁中胆汁酸(BA)排泄呈剂量依赖性降低。由于药物引起的胆汁中水的显著减少,胆汁中BA浓度趋于增加。在5微摩尔时,AmB还导致肝脏对[14C]蔗糖的清除增加以及肝细胞酶释放到灌注液中。这些改变与AmB引起的灌注液流量减少无关。此外,5微摩尔的该药物导致肝脏对胶体碳的清除显著降低。在这种情况下,该作用也与药物引起的灌注液流量减少无关。AmB对大鼠肝脏的毒性作用可解释为细胞膜功能完整性的紊乱,这会导致胆汁淤积、酶泄漏和网状内皮系统功能受损。后一种作用值得仔细评估其临床意义。