Meini S, Mak J C, Rohde J A, Rogers D F
Department of Thoracic Medicine, National Heart & Lung Institute, London, UK.
Neuropeptides. 1993 Feb;24(2):81-9. doi: 10.1016/0143-4179(93)90025-6.
The effects of synthetic tachykinin receptor agonists on mucus secretion by ferret trachea was determined in vitro in Ussing chambers using 35SO4 as a mucus marker and the synthetic peptides [Sar9,Met(O2)11]substance P (SarSP), [beta Ala8]neurokinin A-(4-10) and [MePhe7] neurokinin B which are selective for NK1, NK2 and NK3 tachykinin-receptors respectively. The bronchomotor effects of the same agonists were also studied in vitro and tachykinin receptors were localized by autoradiographic mapping. SarSP was the only synthetic agonist able to elicit a concentration-dependent increase in mucus secretion and was much more potent than SP. The EC50 for SarSP was 1.7 x 10(-6) M. Moreover, the maximal increase in release of 35SO4 produced by SarSP 10(-5) M was 95% of the increase produced by methacholine 10(-4) M indicating that this concentration of SarSP induced a near maximal secretory response. There was no significant difference in the secretory action of SP administered from the luminal or the submucosal side of the tissue. Only the NK2 agonist was able to produce a concentration-dependent contractility of bronchial ring preparations and its effect was relatively weak (EC50 6.4 x 10(-6) M). Capsaicin (10(-5) M) produced only a slight increase in tracheal mucus secretion (28 +/- 5%; n = 6) and was completely ineffective in inducing bronchoconstriction. Binding sites for [125I]-Bolton Hunter SP were more evident than sites for [125I]-NKA on submucosal glands and epithelium. In contrast, only binding sites to NKA could be observed over the smooth muscle.(ABSTRACT TRUNCATED AT 250 WORDS)
采用35SO4作为黏液标记物,在尤斯灌流小室中体外测定了合成速激肽受体激动剂对雪貂气管黏液分泌的影响,所用的合成肽[Sar9,Met(O2)11]P物质(SarSP)、[β丙氨酸8]神经激肽A-(4 - 10)和[甲基苯丙氨酸7]神经激肽B分别对NK1、NK2和NK3速激肽受体具有选择性。还在体外研究了相同激动剂的支气管运动效应,并通过放射自显影定位速激肽受体。SarSP是唯一能引起黏液分泌浓度依赖性增加的合成激动剂,且比P物质更有效。SarSP的EC50为1.7×10(-6)M。此外,10(-5)M的SarSP产生的35SO4释放最大增加量是10(-4)M乙酰甲胆碱产生增加量的95%,表明该浓度的SarSP诱导了接近最大的分泌反应。从组织的管腔侧或黏膜下侧给予P物质,其分泌作用无显著差异。只有NK2激动剂能使支气管环制剂产生浓度依赖性收缩,且其作用相对较弱(EC50为6.4×10(-6)M)。辣椒素(10(-5)M)仅使气管黏液分泌略有增加(28±5%;n = 6),且在诱导支气管收缩方面完全无效。[125I]-博尔顿·亨特P物质的结合位点在黏膜下腺和上皮细胞上比[125I]-神经激肽A的位点更明显。相反,在平滑肌上只能观察到与神经激肽A的结合位点。(摘要截短于250字)