123I-MIBG pulmonary removal: a biochemical marker of minimal lung endothelial cell lesions
123I-MIBG pulmonary removal: a biochemical marker of minimal lung endothelial cell lesions
复制标题
123I-MIBG 肺切除:最小肺内皮细胞病变的生化标志物
DOI:
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发表时间:
2005
期刊:
影响因子:
--
通讯作者:
A. Donath
中科院分区:
文献类型:
--
作者:
D. Slosman;B. Polla,;A. Donath
Circulating biogenic amines, such as serotonin or norepinephrine, are cleared by the lung and can be considered as indicators of pulmonary endothelial integrity. An iodinated norepinephrine analogue, metaiodo-benzylguanidine (MIBG), is extracted in the lung by an active, saturable transport system. In order to investigate the use of MIBG lung extraction to detect minimal,lung endothelial cell lesions, an experimental model of initial pulmonary vascular lesions was developed in rats using repeated daily intraperitoneal injection of bleomycin (BLM: 2 U/100 g body weight) over a 5-day period. At this time, a significant decrease of serum angiotensin-converting enzyme activity, an index of endothelial cell metabolism, was observed (214±11 U/ml in controls as compared with 182±11 U/ml in BLM-treated rats,P < 0.05); electron microscopy showed the presence of typical but minimal endothelial cell lesions (blebbing). MIBG extraction (%EMIBG) was measured using the isolated perfused lung model after a 10-min steady-state period and 2 min of perfusion with123I-MIBG (0.1 μCi/ml) and125I-labelled human serum albumin (HSA) (0.2 μCi/ml). Intraperitoneal administration of BLM to rats for 5 days resulted in a significant decrease in pulmonary extraction of MIBG. %EMIBG declined from a control value of 24.7%±1.1% in controls to 19.3%±1.6% in BLM-treated rats (n=27,P<0.05; -21.2%). HSA lung extraction, used as an estimate of nonspecific residual lung activity, was not different in the lungs of BLM-treated rats as compared with controls. Because measurements of MIBG lung extraction (%EMIBG) were able to demonstrate the presence of minimal endothelial cell lesions due to the BLM toxicity, MIBG is an index of pulmonary endothelial cell function.
DOI:
10.1164/ajrccm/137.1.123
发表时间:
1988
期刊:
The American review of respiratory disease
影响因子:
--
作者:
Johnson,DE;Wobken,JD;Landrum,BG
通讯作者:
Landrum,BG