Sloof G W, Visser F C, Eenige van M J, Comans E F, Teerlink T, Herscheid J D, Van der Vusse G J, Knapp F F
Dept. of Cardiology, Free University Hospital, Amsterdam, The Netherlands.
J Nucl Med. 1993 Apr;34(4):649-57.
The kinetics of 17-[123I]iodoheptadecanoic acid (IHDA), 15-(p-[125I]iodophenyl)pentadecanoic acid (pIPPA) and 15-(p-[131I]iodophenyl)-3,3-dimethylpentadecanoic acid (DMIPPA) were investigated in normal canine myocardium. After simultaneous intravenous injection, myocardial biopsy specimens and samples of arterial blood were taken over 80 min. IHDA showed the highest myocardial uptake (995 +/- 248 dpm/mg.mCi versus pIPPA: 785 +/- 197 dpm/mg.mCi, ns) and the largest size of oxidation (74% +/- 4% versus pIPPA: 65% +/- 5%, p < 0.05). Myocardial activity of IHDA decreased with a half-time value of 11.2 min (pIPPA: 13.2 min). Phospholipids were the main lipid fraction into which IHDA was incorporated, whereas pIPPA was predominantly incorporated into triacylglycerols. DMIPPA myocardial activity remained constant during the assay period and instead of being oxidized, DMIPPA was mainly incorporated into triacylglycerols (55% +/- 12%). The myocardium-to-blood ratios of DMIPPA were greater than 10:1. The ratios at peak for IHDA and pIPPA were 4.1:1 and 3.9:1, respectively (both p < 0.0001 versus DMIPPA). In conclusion, differences have been found in the myocardial uptake, oxidation and lipid distribution of IHDA, pIPPA and DMIPPA. DMIPPA is a promising tracer for fatty acid uptake studies with single-photon emission computerized tomography because of its prolonged retention and high myocardium-to-blood ratios.
在正常犬心肌中研究了17-[123I]碘十七烷酸(IHDA)、15-(对-[125I]碘苯基)十五烷酸(pIPPA)和15-(对-[131I]碘苯基)-3,3-二甲基十五烷酸(DMIPPA)的动力学。同时静脉注射后,在80分钟内采集心肌活检标本和动脉血样本。IHDA显示出最高的心肌摄取量(995±248 dpm/mg·mCi,与pIPPA相比:785±197 dpm/mg·mCi,无显著差异)和最大的氧化量(74%±4%,与pIPPA相比:65%±5%,p<0.05)。IHDA的心肌活性以11.2分钟的半衰期下降(pIPPA:13.2分钟)。磷脂是IHDA掺入的主要脂质部分,而pIPPA主要掺入三酰甘油中。在测定期间,DMIPPA的心肌活性保持恒定,并且DMIPPA不是被氧化,而是主要掺入三酰甘油中(55%±12%)。DMIPPA的心肌与血液的比率大于10:1。IHDA和pIPPA在峰值时的比率分别为4.1:1和3.9:1(与DMIPPA相比,两者p<0.0001)。总之,在IHDA、pIPPA和DMIPPA的心肌摄取、氧化和脂质分布方面发现了差异。由于其延长的滞留时间和高心肌与血液的比率,DMIPPA是用于单光子发射计算机断层扫描脂肪酸摄取研究的一种有前景的示踪剂。