Henseling M, Eckert E, Trendelenburg U
Naunyn Schmiedebergs Arch Pharmacol. 1976;292(3):231-41. doi: 10.1007/BF00517383.
Reserpine-pretreated or normal rabbit aortic strips (whose noradrenaline-metabolizing enzymes were inhibited by treatment with 0.5 mM pargyline and by the presence of 0.1 mM U-0521) were incubated with 1.18 muM labelled noradrenaline for 30 min. Subsequently, strips were either analysed or washed out with amine-free solution for 240 to 250 min. From the efflux curves the original distribution of radioactivity was estimated by compartmental analysis. 1. The accumulation of radioactivity in the strips was reduced by 30 muM cocaine to that observed for nerve-free strips. In reserpine-pretreated strips this was due to a partial reduction of the filling of comartment IV (characterized by a half time of efflux of 10 to 20 min; earlier evidence had already shown that part of this compartment is of neuronal origin; Hensling et al., 1976) and a pronounced decrease of the filling of compartment V (characterized by the longest half time). In normal strips the same changes were observed as well as pronounced reduction of the "bound fraction". Thus, cocaine reduced the filing of those compartments which had been identified as neuronal ones (Henseling et al., 1976). 2. When 30 muM cocaine was added to the wash out solution only, the neuronal efflux of radioactivity from reserpine-pretreated strips was accelerated, while the efflux from extraneuronal or extracellular compartments remained unaffected. This effect of cocaine was the same for (-)- and (+)noradrenaline, and its was not significaltly decreased when paired strips exposed to an inhibitor of extraneuronal uptake (86 muM corticosterone) throughout the experiment. In normal strips, cocaine had very little or no effect on the efflux of radioactivity. 3. The results are consistent with the view that cocaine impairs the influx of amine into the neurone, while block of re-uptake of unchanged amine is one of the determinants of its effect on the rate of efflux from the axoplasm. Comparison of efflux curves with corresponding relaxation curves (determined in the absence and presence of cocaine) indicates that, when both noradrenaline-metabolizing enzymes are inhibited, relaxation of the strips is accounted for by a) the efflux of unchanged amine from neuronal (and extraneuronal) stores and b) the sensitivity of the preparation to noradrenaline.
用利血平预处理或正常的兔主动脉条(其去甲肾上腺素代谢酶通过用0.5 mM优降宁处理以及存在0.1 mM U - 0521而被抑制)与1.18 μM标记的去甲肾上腺素孵育30分钟。随后,对主动脉条进行分析,或者用无胺溶液冲洗240至250分钟。根据流出曲线,通过房室分析估计放射性的原始分布。1. 30 μM可卡因使主动脉条中放射性的积累减少至无神经主动脉条所观察到的水平。在利血平预处理的主动脉条中,这是由于IV房室(其流出半衰期为10至20分钟;早期证据已表明该房室的一部分起源于神经元;亨斯林等人,1976年)的填充部分减少以及V房室(其具有最长的半衰期)的填充显著减少。在正常主动脉条中也观察到了相同的变化以及“结合部分”的显著减少。因此,可卡因减少了那些已被确定为神经元房室(亨斯林等人,1976年)的填充。2. 仅在冲洗溶液中加入30 μM可卡因时,利血平预处理的主动脉条中放射性的神经元流出加速,而神经外或细胞外房室的流出不受影响。可卡因对(-)-和(+)-去甲肾上腺素的这种作用相同,并且当配对的主动脉条在整个实验中暴露于神经外摄取抑制剂(86 μM皮质酮)时,其作用没有显著降低。在正常主动脉条中,可卡因对放射性流出几乎没有影响或没有影响。3. 这些结果与以下观点一致,即可卡因损害胺进入神经元的流入,而阻止未改变的胺的再摄取是其对轴浆流出速率影响的决定因素之一。将流出曲线与相应的舒张曲线(在有无可卡因的情况下测定)进行比较表明,如果两种去甲肾上腺素代谢酶均被抑制,主动脉条的舒张是由以下因素引起的:a)未改变的胺从神经元(和神经外)储存中的流出,以及b)制剂对去甲肾上腺素的敏感性。