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离体大鼠肺肺泡和毛细血管空间中5-羟色胺摄取的比较。

Comparison of serotonin uptake from the alveolar and capillary spaces of isolated rat lung.

作者信息

Fisher A B, Pietra G G

出版信息

Am Rev Respir Dis. 1981 Jan;123(1):74-8. doi: 10.1164/arrd.1981.123.1.74.

DOI:10.1164/arrd.1981.123.1.74
PMID:7458089
Abstract

The role of pulmonary epithelium in the clearance of 5-hydroxytryptamine (5-HT) was evaluated by measuring uptake of the amine by the isolated rat lung during vascular perfusion or after endotracheal instillation. During perfusion with 0.5 microM of [14C]5-HT, the initial rate of uptake was 5.3 +/- 0.14 nmol/min (mean +/- SE; n = 19). Autoradiography with [3H]5-HT demonstrated localization of grains predominantly over the pulmonary endothelium with a grain density/mu2 of 0.78 compared with 0.05 to 0.21 for other structures of the alveolar septum. When 0.5 microM of [14C]5-HT was instilled into the air spaces, the rate of uptake was 0.15 +/- 0.005 nmol/min (n = 4), and increased to 0.25 +/- 0.05 nmol/min (n = 6) with instillation of 1 microM of 5-HT. Uptake from the air spaces was inhibited by 72% in the presence of 0.5 mM of imipramine. Autoradiography after instillation of [3H]5-HT into the trachea showed localization of developed silver grains over both alveolar epithelium and endothelium; the grain density/mu2 was greatest in endothelial cells, and significantly exceeded the predicted value based on uniform distribution only for this compartment. The results indicate that alveolar epithelium compared with pulmonary capillary endothelium has very limited capacity to accumulate 5-HT.

摘要

通过在血管灌注期间或气管内滴注后测量分离的大鼠肺对胺的摄取,评估肺上皮在5-羟色胺(5-HT)清除中的作用。在用0.5微摩尔[14C]5-HT灌注期间,初始摄取率为5.3±0.14纳摩尔/分钟(平均值±标准误;n = 19)。用[3H]5-HT进行放射自显影显示,颗粒主要定位于肺内皮,颗粒密度/平方微米为0.78,而肺泡隔其他结构的颗粒密度为0.05至0.21。当将0.5微摩尔[14C]5-HT滴入气腔时,摄取率为0.15±0.005纳摩尔/分钟(n = 4),滴入1微摩尔5-HT时摄取率增加至0.25±0.05纳摩尔/分钟(n = 6)。在存在0.5毫摩尔丙咪嗪的情况下,从气腔的摄取受到72%的抑制。将[3H]5-HT滴入气管后的放射自显影显示,显影的银颗粒定位于肺泡上皮和内皮;颗粒密度/平方微米在内皮细胞中最大,并且仅基于该隔室的均匀分布显著超过预测值。结果表明,与肺毛细血管内皮相比,肺泡上皮积累5-HT的能力非常有限。

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Environ Health Perspect. 1984 Apr;55:139-48. doi: 10.1289/ehp.8455139.