Mastrangelo D, Mathison R
J Cardiovasc Pharmacol. 1983 Jan-Feb;5(1):98-101.
Three preparations of the rat hepatic portal vein, everted, noneverted, and longitudinal strip, were examined for their responsiveness to noradrenaline (NA), substance P (SP), and eledoisin (ED). The longitudinal strips and the everted veins exhibited similar sensitivities to these compounds, whereas the noneverted vein was two to four times less sensitive. The time course to generation of a maximal response was markedly slower for the noneverted vein. The poor reactivity of the noneverted vein is attributed to a reduced accessibility of the compounds to receptor sites. The myogenic responses of the longitudinal strips to NA and ED but not SP were characterized by a tonic-type contracture, whereas everted and noneverted preparations responded to the peptides, at low and intermediate concentrations, with large-amplitude and long-duration contractions. The everted vein is presented as a useful preparation for evaluation of drug-receptor interactions.
对大鼠肝门静脉的三种制剂,即外翻、未外翻和纵向条带制剂,检测了它们对去甲肾上腺素(NA)、P物质(SP)和依地多辛(ED)的反应性。纵向条带和外翻静脉对这些化合物表现出相似的敏感性,而未外翻静脉的敏感性则低两到四倍。未外翻静脉产生最大反应的时间进程明显较慢。未外翻静脉反应性差归因于化合物与受体部位的可及性降低。纵向条带对NA和ED而非SP的肌源性反应的特征是强直性挛缩,而外翻和未外翻制剂在低和中等浓度下对这些肽的反应是大幅度和长时间的收缩。外翻静脉被认为是评估药物 - 受体相互作用的有用制剂。