Lembeck F, Amann R, Barthó L
Naunyn Schmiedebergs Arch Pharmacol. 1986 Jul;333(3):290-3. doi: 10.1007/BF00512943.
Two tachykinin antagonists, [D-Pro2, D-Trp7,9]-substance P (AP-2) and [D-Arg1, D-Trp7,9, L-Leu11]-substance P (spantide) were injected or infused intraarterially into the isolated perfused rabbit ear connected to the body via the nerve only. The effects of these antagonists on venous outflow, release of histamine, and on acetylcholine-induced reflex fall in blood pressure were recorded. The effect of spantide was also investigated on cholinergic "twitch" responses to the isolated field stimulated ileum of the guinea-pig. Bolus injections of AP-2 (6.6 nmol and 20 nmol) and spantide 20 nmol and 66 nmol i.a. caused a dose-dependent reduction in venous outflow, which could mainly be explained by the release of histamine since the histamine H1 receptor blocker mepyramine inhibited this effect; release of histamine was also directly demonstrated. Injections of AP-2 (20 nmol) and spantide (66 nmol) caused nociceptor stimulation which might in part result from the histamine release. The reflex fall in blood pressure due to nociceptor stimulation by acetylcholine was reduced by less than 30% by infusion of the tachykinin antagonists in a concentration of 12 mumol l-1 but not at 2.4 mumol l-1. Spantide (up to 100 mumol l-1) did not inhibit electrically evoked "twitch" responses of the guinea-pig ileum. The local anaesthetic drug procaine (4.2-42 mumol l-1) inhibited these contractions in a concentration-dependent manner. It is concluded that the tachykinin antagonists might show effects which are not related to their specific tachykinin antagonistic action as indicated by the findings in the rabbit ear.(ABSTRACT TRUNCATED AT 250 WORDS)
将两种速激肽拮抗剂,即[D-脯氨酸2,D-色氨酸7,9]-P物质(AP-2)和[D-精氨酸1,D-色氨酸7,9,L-亮氨酸11]-P物质(速激肽拮抗剂)仅通过神经动脉内注射或输注到与身体相连的离体灌注兔耳中。记录了这些拮抗剂对静脉流出、组胺释放以及乙酰胆碱诱导的血压反射性下降的影响。还研究了速激肽拮抗剂对豚鼠离体肠段电场刺激引起的胆碱能“抽搐”反应的影响。动脉内推注AP-2(6.6纳摩尔和20纳摩尔)和速激肽拮抗剂20纳摩尔和66纳摩尔导致静脉流出呈剂量依赖性减少,这主要可由组胺释放来解释,因为组胺H1受体阻滞剂美吡拉敏可抑制这种作用;组胺释放也得到了直接证实。注射AP-2(20纳摩尔)和速激肽拮抗剂(66纳摩尔)引起伤害感受器刺激,这可能部分是由组胺释放所致。通过输注浓度为12微摩尔/升的速激肽拮抗剂,乙酰胆碱引起的伤害感受器刺激导致的血压反射性下降降低了不到30%,但在2.4微摩尔/升时则没有降低。速激肽拮抗剂(高达100微摩尔/升)并未抑制豚鼠回肠的电诱发“抽搐”反应。局部麻醉药普鲁卡因(4.2 - 42微摩尔/升)以浓度依赖性方式抑制这些收缩。得出的结论是,速激肽拮抗剂可能表现出与其在兔耳中的发现所表明的特异性速激肽拮抗作用无关的效应。(摘要截短至250字)