Hays M T, Berman M
J Nucl Med. 1977 Sep;18(9):898-904.
Using a primed infusion technique, distribution of pertechnetate was monitored in normal volunteer subjects over an 8-hr period. Two groups of subjects were studied, during hours 0-4 (n = 8) and hours 4-8 (n = 7), respectively, of the infusion. At 6.5 hr a large dose of NaI (1000 mg) was administered intravenously to the second group. Plasma, salivary, and urinary radioactivities were assayed, and external counts were made of radioactivities over the neck, thigh, and right upper abdomen. A kinetic model was developed for pertechnetate based upon the distribution data, the iodide perturbation, and known physiology for pertechnetate and iodide. The model has three major subsystems: (1) the thyroid trap; (2) a whole-body distribution, containing plasma and two extravascular compartments; and (3) the gastrointestinal tract, including the salivary, stomach (including upper small intestine), and two lower intestinal compartments. One of the latter, which turns over very slowly, is believed to represent bowel wall. The large NaI dose markedly reduced transport into compartments of the thyroid trap, the saliva, and the stomach and small intestine. This study shows that, in most respects, pertechnetate is distributed qualitatively but not quantitatively like iodide but that, unlike iodide, large bowel distribution plays an important role, especially in long-term studies.
采用预充输注技术,在8小时内对正常志愿者体内高锝酸盐的分布进行监测。分别在输注的0至4小时(n = 8)和4至8小时(n = 7)对两组受试者进行研究。在6.5小时时,对第二组受试者静脉注射大剂量的碘化钠(1000毫克)。测定血浆、唾液和尿液中的放射性,并对颈部、大腿和右上腹的放射性进行体外计数。基于分布数据、碘化物扰动以及高锝酸盐和碘化物的已知生理学特性,建立了高锝酸盐的动力学模型。该模型有三个主要子系统:(1)甲状腺捕获器;(2)全身分布,包括血浆和两个血管外隔室;(3)胃肠道,包括唾液腺、胃(包括小肠上段)和两个下段肠道隔室。后者中的一个隔室周转非常缓慢,据信代表肠壁。大剂量的碘化钠显著减少了进入甲状腺捕获器、唾液、胃和小肠隔室的转运。这项研究表明,在大多数方面,高锝酸盐的分布在定性上与碘化物相似,但在定量上不同,而且与碘化物不同的是,大肠分布起着重要作用,尤其是在长期研究中。