Stoeckel K, Guroff G, Schwab M, Thoenen H
Brain Res. 1976 Jun 11;109(2):271-84. doi: 10.1016/0006-8993(76)90530-8.
The present study has shown that after intravenous injection of [125I]NGF the time-course of appearance of radioactivity in all organs studied with the exception of sympathetic and sensory ganglia, roughly paralleled that of the blood. The highest levels were reached immediately after injection, after which the radioactivity decayed rapidly within the firsh hour. By contrast, in the superior cervical ganglion there was a small but significant increase within the first hour. After this the radioactivity remained constant for about 4 h and then increased dramatically (7-fold) when the radioactivity in other tissues had declined to very low levels. Measuring the proportion of radioactivity in the plasma which represents immunologically active NGF, we found that within 30 min after injection all the radioactivity represented unchanged [125I]NGF. After this time the proportion of immunologically active NGF decreased gradually and reached a final level of about 10-15%. Evidence that the radioactivity accumulated in the superior cervical ganglion by retrograde axonal transport represents unchanged [125I]NGF was provided by gel electrophoresis. The results are interpreted as follows: the initial small increase in the sympathetic ganglia may result either from [125I]NGF taken up by short collateral fibres within the ganglion or from a direct accumulation of blood-borne [125I]NGF by the cell bodies of the adrenergic neurones. The dramatic increase occurring after 4 h is caused by the moiety of [125I]NGF reaching the cell body by retrograde axonal transport. This interpretation is supported by autoradiographic studies which showed that 1 h after [125I]NGF injection there was only very sparse labelling of the ganglion, whereas 24 h later virtually all the cell bodies were heavily labelled. Moreover, it could be shown that the lag period between intravenous injection and subsequent accumulation of [125I]NGF in the adrenergic cell bodies was considerably shorter after transection of the postganglionic fibres distal to the cell body [the transected fibres were allowed to regenerate for 7 days] resulting in a reduction of the distance between the site of uptake and accumulation.
本研究表明,静脉注射[125I]神经生长因子(NGF)后,除交感神经节和感觉神经节外,所有研究器官中放射性出现的时间进程大致与血液平行。注射后立即达到最高水平,之后放射性在最初1小时内迅速衰减。相比之下,颈上神经节在最初1小时内有少量但显著的增加。在此之后,放射性保持恒定约4小时,然后在其他组织中的放射性降至非常低的水平时急剧增加(7倍)。通过测量血浆中代表免疫活性NGF的放射性比例,我们发现注射后30分钟内所有放射性均代表未变化的[125I]NGF。此后,免疫活性NGF的比例逐渐降低,最终达到约10 - 15%的水平。凝胶电泳提供了证据,表明通过逆行轴突运输在颈上神经节中积累的放射性代表未变化的[125I]NGF。结果的解释如下:交感神经节中最初的少量增加可能是由于神经节内短侧支纤维摄取的[125I]NGF,或者是肾上腺素能神经元细胞体直接积累血源性[125I]NGF所致。4小时后出现的急剧增加是由通过逆行轴突运输到达细胞体的[125I]NGF部分引起的。放射自显影研究支持了这一解释,该研究表明,[125I]NGF注射1小时后神经节的标记非常稀疏,而24小时后几乎所有细胞体都被大量标记。此外,可以证明,在切断细胞体远端的节后纤维[切断的纤维允许再生7天]后,静脉注射与随后[125I]NGF在肾上腺素能细胞体中积累之间的延迟期明显缩短,导致摄取部位与积累部位之间的距离减小。