Sugihara M, Todoki K, Okabe E
Department of Pharmacology, Kanagawa Dental College, Japan.
Nihon Yakurigaku Zasshi. 1991 Aug;98(2):63-71. doi: 10.1254/fpj.98.2_63.
The effect of intravenous injection of 10 micrograms of a lipopolysaccharide (endotoxin) extracted from E. coli to rabbits on the responses of isolated lingual arteries to des-Arg9-bradykinin (a specific kinins B1-receptor agonist) was studied. Endotoxin injection led to the appearance of the endothelium-independent contractile effect of des-Arg9-bradykinin in the arteries; endotoxin elicited this response when administered at 1, 5 or 20 hr before the experiment, in a time-interval dependent manner. The contractile response to des-Arg9-bradykinin of the arteries isolated from animals receiving endotoxin 20 hr before the experiment was attenuated by des-Arg9-[Leu8]-bradykinin (a specific inhibitor of kinins B1-receptor) or pretreatment of the animals with an inhibitor of protein synthesis (cycloheximide and actinomycin D). When compared with the effect of des-Arg9-bradykinin, bradykinin (a potent kinin B2-receptor, but weak B1-receptor stimulant) caused slight contraction of the arteries; however, this effect was not endotoxin-dependent and was not modified by des-Arg9-[Leu8]-bradykinin. Effect of in vitro preincubation with endotoxin of the arteries isolated from animals receiving saline 20 hr before the experiment was further studied. The preincubation (for 1 and 5 hr) with endotoxin of the arteries in the presence or absence of plasma had no effect on the sensitivity of the arteries to des-Arg9-bradykinin; the sensitivity was also unaffected in the presence or absence of endotoxin, thus suggesting that there is no interaction between endotoxin and some plasma-related factors with the appearance of the contraction in response to the kinin B1-receptor agonist in the arteries in vitro.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了给家兔静脉注射10微克从大肠杆菌中提取的脂多糖(内毒素)对离体舌动脉对去-精氨酸9-缓激肽(一种特异性激肽B1受体激动剂)反应的影响。注射内毒素导致动脉中去-精氨酸9-缓激肽出现非内皮依赖性收缩效应;在内毒素于实验前1、5或20小时给药时,会以时间间隔依赖性方式引发这种反应。对于在实验前20小时接受内毒素的动物所分离出的动脉,其对去-精氨酸9-缓激肽的收缩反应会被去-精氨酸9-[亮氨酸8]-缓激肽(一种激肽B1受体特异性抑制剂)或用蛋白质合成抑制剂(环己酰亚胺和放线菌素D)对动物进行预处理所减弱。与去-精氨酸9-缓激肽的作用相比,缓激肽(一种强效激肽B2受体激动剂,但对B1受体刺激作用较弱)会引起动脉轻微收缩;然而,这种效应不依赖于内毒素,且不受去-精氨酸9-[亮氨酸8]-缓激肽的影响。进一步研究了对在实验前20小时接受生理盐水的动物所分离出的动脉进行内毒素体外预孵育的效果。在有或无血浆存在的情况下,动脉与内毒素预孵育(1和5小时)对动脉对去-精氨酸9-缓激肽的敏感性没有影响;在有或无内毒素存在时敏感性也不受影响,因此表明在内毒素与一些血浆相关因子之间不存在相互作用,从而不会在体外引发动脉对激肽B1受体激动剂的收缩反应。(摘要截短于250字)