Bryan L J, O'Donnell S R, Wildsoet C F
Naunyn Schmiedebergs Arch Pharmacol. 1984 Sep;327(2):133-8. doi: 10.1007/BF00500907.
In smooth muscle or cartilage preparations of guinea-pig trachea incubated in 0.1 mumol/l 3H-isoprenaline, extraneuronal uptake inhibitors (corticosterone, normetanephrine, phenoxybenzamine) caused only partial inhibition (64-75%) of the formation of 3-O-methylisoprenaline. Thus, isoprenaline appeared to be exposed to catechol-O-methyltransferase by diffusional entry as well as by extraneuronal uptake in both the smooth muscle and cartilage regions of the trachea. Fluorescence microphotometric measurements of catecholamine uptake in trachealis smooth muscle cells, when tissues were incubated in 200 or 1,200 mumol/l isoprenaline, adrenaline or noradrenaline in the absence and presence of extraneuronal uptake inhibitors (corticosterone, normetanephrine, phenoxybenzamine), showed that the contribution of diffusional entry to the uptake of the amines into the cells fitted with the order of their lipophilicities, viz. isoprenaline much greater than adrenaline greater than noradrenaline. A kinetic analysis of the uptake of isoprenaline into the trachealis smooth muscle cells was carried out in the absence and presence of 100 mumol/l corticosterone. The kinetic analysis (a) showed that the corticosterone-resistant component of total uptake was not saturable, supporting the view that it represented diffusional entry of isoprenaline into the cells, and (b) provided Km and Vmax values (112 mumol/l and 101 F/min, respectively) for the saturable extraneuronal uptake of isoprenaline into the cells. The study provided evidence for marked diffusional entry of the lipophilic amine isoprenaline into guinea-pig trachealis smooth muscle cells. The diffusional entry of adrenaline was much less and that of noradrenaline negligible.(ABSTRACT TRUNCATED AT 250 WORDS)
在豚鼠气管的平滑肌或软骨制剂中,于0.1 μmol/L 3H-异丙肾上腺素中孵育时,神经外摄取抑制剂(皮质酮、去甲变肾上腺素、酚苄明)仅引起3-O-甲基异丙肾上腺素形成的部分抑制(64 - 75%)。因此,在气管的平滑肌和软骨区域,异丙肾上腺素似乎通过扩散进入以及神经外摄取而暴露于儿茶酚-O-甲基转移酶。当组织在有无神经外摄取抑制剂(皮质酮、去甲变肾上腺素、酚苄明)的情况下于200或1200 μmol/L异丙肾上腺素、肾上腺素或去甲肾上腺素中孵育时,对气管平滑肌细胞中儿茶酚胺摄取的荧光显微光度测量表明,扩散进入对胺类进入细胞的贡献与其亲脂性顺序相符,即异丙肾上腺素远大于肾上腺素大于去甲肾上腺素。在有无100 μmol/L皮质酮的情况下对异丙肾上腺素进入气管平滑肌细胞的摄取进行了动力学分析。动力学分析(a)表明,总摄取中对皮质酮耐药的部分不饱和,支持其代表异丙肾上腺素扩散进入细胞的观点,(b)提供了异丙肾上腺素进入细胞的可饱和神经外摄取的Km和Vmax值(分别为112 μmol/L和101 F/min)。该研究为亲脂性胺异丙肾上腺素显著扩散进入豚鼠气管平滑肌细胞提供了证据。肾上腺素的扩散进入少得多,而去甲肾上腺素的扩散进入可忽略不计。(摘要截断于250字)