Moser K M, Kidikoro Y, Marsh J, Sgroi V
J Lab Clin Med. 1978 Feb;91(2):214-22.
Highly purified A-1-A.T., prepared from blood obtained from donors of known PiZZ and PiMM phenotype, was radiolabeled with 125I or 131I and injected intravenously into dogs. The radiolabeled proteins retained their prelabel electrophoretic and trypsin-inhibitory characteristics. The biologic t1/2 of both M and Z protein in the circulation were similar, averaging 71 hr for M protein and 80 hr for Z protein. The label was shown to remain tightly bound in vivo for 2 days after injection. The material was nonpyrogenic in rabbit and dog. No arteriovenous differences in radioactivity could be detected at 2 or 20 min after injection. However, surface scanning disclosed substantial pulmonary deposition of radioactivity for the first 9 hr after injection. At 48 hr, intense radioactivity was present in the spleen, but not in the liver. These studies indicate the feasibility of similar studies in man, including noninvasive assessment of body distribution of M and Z protein by surface scanning techniques.
从已知PiZZ和PiMM表型的献血者血液中制备的高度纯化的α1-抗胰蛋白酶(A-1-A.T.),用125I或131I进行放射性标记,然后静脉注射到狗体内。放射性标记的蛋白质保留了其标记前的电泳和胰蛋白酶抑制特性。循环中M蛋白和Z蛋白的生物学半衰期相似,M蛋白平均为71小时,Z蛋白平均为80小时。注射后2天内,标记物在体内仍紧密结合。该物质对兔和狗无致热原性。注射后2分钟或20分钟未检测到放射性的动静脉差异。然而,表面扫描显示注射后最初9小时肺部有大量放射性沉积。48小时时,脾脏有强烈放射性,但肝脏没有。这些研究表明在人体进行类似研究的可行性,包括通过表面扫描技术对M蛋白和Z蛋白的体内分布进行无创评估。