Blume J, Palmié S, Aue B, Spielmann R P, Sievers E, Lodemann K P, Heller M
Universitätsklinik für Radiologische Diagnostik, Klinikum, Christian-Albrechts-Universität, Kiel, Germany.
Acad Radiol. 1994 Nov;1(3):253-60. doi: 10.1016/s1076-6332(05)80725-1.
Pancreatic and hepatic contrast enhancement after different modes of administration of Mn-bis pyridoxal ethylene diamine diacetic acid (Mn-DPDP) and the influence of the hormones secretin and cholecystokinin on the uptake of this new contrast agent were studied by using magnetic resonance (MR) imaging and atomic absorption spectroscopy (AAS) examinations carried out on 13 young domestic pigs.
Mn-DPDP was administered either as bolus injection or 30-min infusion. The course of contrast enhancement was noted. MR imaging was carried out with or without pancreatic stimulation. The Mn content in pancreatic and hepatic tissue was analyzed by using AAS.
Mn-DPDP caused a significant increase (66 +/- 40.1%) in pancreatic signal intensity, an increase in hepatic signal intensity (78 +/- 23.0%), and a significantly higher Mn content on tissue samples of both organs. The results showed a wide individual range. With infusion of Mn-DPDP, pancreatic enhancement was slower, with a peak at 82 +/- 34 min compared with 54 +/- 51 min following bolus injection. The Mn content of both hepatic and pancreatic tissue determined by AAS seemed to be higher after infusion. An incomplete washout of Mn after 24 hr was demonstrated. Hormonal stimulation of the pancreas further increased pancreatic signal intensity but did not influence hepatic contrast enhancement.
Infusion is the method of choice for administering Mn-DPDP because it causes an increase in hepatic signal intensity but does not change pancreatic enhancement. Although pancreatic hormonal stimulation intensifies enhancement, the increase is not statistically significant, and this practice will not contribute to day-to-day clinical practice.
通过对13只幼年家猪进行磁共振成像(MR)和原子吸收光谱(AAS)检查,研究了双吡啶醛乙二胺二乙酸锰(Mn-DPDP)不同给药方式后的胰腺和肝脏对比增强情况,以及激素促胰液素和胆囊收缩素对这种新型造影剂摄取的影响。
Mn-DPDP采用静脉推注或30分钟输注给药。记录对比增强过程。在有或无胰腺刺激的情况下进行MR成像。使用AAS分析胰腺和肝脏组织中的锰含量。
Mn-DPDP使胰腺信号强度显著增加(66±40.1%),肝脏信号强度增加(78±23.0%),且两个器官的组织样本中锰含量显著更高。结果显示个体差异较大。输注Mn-DPDP时,胰腺增强较慢,峰值出现在82±34分钟,而静脉推注后为54±51分钟。AAS测定的肝脏和胰腺组织中的锰含量在输注后似乎更高。24小时后显示锰的清除不完全。胰腺的激素刺激进一步增加了胰腺信号强度,但不影响肝脏对比增强。
输注是给予Mn-DPDP的首选方法,因为它会增加肝脏信号强度,但不改变胰腺增强。尽管胰腺激素刺激会增强增强效果,但增加不具有统计学意义,且这种做法对日常临床实践无帮助。