Elmståhl Barbara, Nyman Ulf, Leander Peter, Chai Chun-Ming, Golman Klaes, Björk Jonas, Almén Torsten
Department of Diagnostic Radiology, Malmö University Hospital, Lund University, SE-205 02, Malmö, Sweden.
Eur Radiol. 2006 Dec;16(12):2712-20. doi: 10.1007/s00330-006-0357-4. Epub 2006 Aug 5.
A study was undertaken of the role of osmotoxicity in gadolinium (Gd) and iodine contrast media (CM) nephrotoxicity in ischemic porcine kidneys. Test solutions: mannitol iso-osmotic to 0.5 M: gadopentetate (1.96 Osm/kg H2O), 0.5 M: gadodiamide (0.78 Osm/kg H2O) and 0.5 M: iohexol (190 mg I/ml, 0.42 Osm/kg H2O). Each solution was injected [3 ml/kg body weight (BW)] into the balloon-occluded (10 min) renal artery of eight left-sided nephrectomized pigs. The plasma half-life of a glomerular filtration rate (GFR) marker was used to compare their effects on GFR 1-3 h post-injection. The median half-lives of the GFR marker after injection of gadopentetate (1,730 min) and mannitol 1.96 Osm/kg H2O (2,782 min) did not differ statistically (P = 0.28), but were significantly longer than after all other solutions (P < 0.001). There was no significant difference (P = 0.06) between gadodiamide (218 min) and mannitol 0.82 Osm/kg H2O (169 min), while there was (P = 0.03) between iohexol (181 min) and mannitol 0.43 Osm/kg H2O (148 min). The difference between gadodiamide and iohexol was significant (P = 0.01). Reduction in GFR, as a marker of nephrotoxicity, induced by gadopentetate correlated with its high osmolality, while the effect of gadodiamide and iohexol may include chemotoxicity. Iohexol molecules were less nephrotoxic than the Gd-CM molecules and contain three-times the number of attenuating atoms per molecule.
一项关于渗透毒性在缺血性猪肾中钆(Gd)和碘造影剂(CM)肾毒性中的作用的研究。测试溶液:与0.5M等渗的甘露醇:钆喷酸葡胺(1.96 Osm/kg H₂O)、0.5M:钆双胺(0.78 Osm/kg H₂O)和0.5M:碘海醇(190mg I/ml,0.42 Osm/kg H₂O)。将每种溶液[3ml/kg体重(BW)]注入八只左侧肾切除猪的球囊阻塞(10分钟)肾动脉。用肾小球滤过率(GFR)标志物的血浆半衰期来比较它们在注射后1 - 3小时对GFR的影响。注射钆喷酸葡胺(1730分钟)和1.96 Osm/kg H₂O的甘露醇(2782分钟)后GFR标志物的中位半衰期在统计学上无差异(P = 0.28),但显著长于所有其他溶液后的半衰期(P < 0.001)。钆双胺(218分钟)和0.82 Osm/kg H₂O的甘露醇(169分钟)之间无显著差异(P = 0.06),而碘海醇(181分钟)和0.43 Osm/kg H₂O的甘露醇(148分钟)之间有差异(P = 0.03)。钆双胺和碘海醇之间的差异显著(P = 0.01)。作为肾毒性标志物的GFR降低,由钆喷酸葡胺诱导,与其高渗透压相关,而钆双胺和碘海醇的作用可能包括化学毒性。碘海醇分子的肾毒性低于Gd - CM分子,且每个分子含有的衰减原子数是Gd - CM分子的三倍。