Bailey S J, Lippe I T, Holzer P
Naunyn Schmiedebergs Arch Pharmacol. 1987 Mar;335(3):296-300. doi: 10.1007/BF00172800.
The effect of the tachykinin antagonist, [D-Pro4, D-Trp7,9,10] substance P-(4-11), on inositol phosphate accumulation produced by tachykinins and by histamine in strips of longitudinal muscle from the guinea-pig small intestine was investigated in the presence of 12 mM Li+. The two tachykinins substance P (SP) and kassinin (20 nM-20 microM) caused an accumulation of inositol phosphates in a concentration-dependent manner. This was seen with an agonist contact time of only 30 s. SP and kassinin were roughly equipotent in inducing inositol phosphate accumulation, which is consistent with their relative potencies in causing muscle contraction. The tachykinin antagonist (20 microM) produced a shift to the right of the dose-response curves for inositol phosphate accumulation caused by SP and kassinin. However, the effect of kassinin was inhibited much more than that of SP, which is consistent with a similar differential antagonism of the contractions induced by these agonists. The tachykinin antagonist also depressed histamine-induced accumulation of inositol phosphates whereas histamine-induced contractions had previously been found unaffected by the antagonist. These findings show that the tachykinin antagonist is not totally selective with regard to agonist-induced accumulation of inositol phosphates in intestinal smooth muscle. This may suggest that the antagonist not only acts on tachykinin receptors but also has another site of cellular action.
在12 mM Li⁺存在的情况下,研究了速激肽拮抗剂[D-脯氨酸⁴,D-色氨酸⁷,⁹,¹⁰]P物质-(4-11)对豚鼠小肠纵肌条中速激肽和组胺诱导的肌醇磷酸积累的影响。两种速激肽P物质(SP)和蛙皮素(20 nM - 20 μM)以浓度依赖性方式引起肌醇磷酸积累。这在激动剂接触时间仅为30秒时即可观察到。SP和蛙皮素在诱导肌醇磷酸积累方面大致等效,这与其引起肌肉收缩的相对效力一致。速激肽拮抗剂(20 μM)使由SP和蛙皮素引起的肌醇磷酸积累的剂量反应曲线向右移动。然而,蛙皮素的作用比SP受到的抑制要大得多,这与这些激动剂诱导的收缩的类似差异拮抗作用一致。速激肽拮抗剂还抑制组胺诱导的肌醇磷酸积累,而此前发现组胺诱导的收缩不受该拮抗剂影响。这些发现表明,速激肽拮抗剂在肠道平滑肌中对激动剂诱导的肌醇磷酸积累并非完全具有选择性。这可能表明该拮抗剂不仅作用于速激肽受体,还具有另一个细胞作用位点。