Marsault R, Vigne P, Frelin C
Institut de Pharmacologie Moléculaire et Cellulaire, Valbonne, France.
Biochem Biophys Res Commun. 1991 Sep 30;179(3):1408-13. doi: 10.1016/0006-291x(91)91729-v.
The irreversibility of the contractile action of endothelin-1 (Et) and of its binding to its receptors are usually believed to be linked in a direct manner. Rat aortic strips were exposed to 25 nM Et for short periods of time that were sufficient to irreversibly saturate membrane receptor sites and then washed of unbound Et. Under these conditions, fast and transient contractile responses were observed. They were unlike the slow and irreversible contractions observed in the continued presence of the peptide. They were as fast as KCl, angiotensin II and vasopressin contractions. It is concluded that the irreversibility of Et contractions and of its interaction with its receptors can be uncoupled. The data also suggests that recycling of endocytosed Et receptors contributes to the sustained contractile action of the peptide.
通常认为,内皮素 -1(Et)的收缩作用及其与受体结合的不可逆性以直接方式相联系。将大鼠主动脉条短时间暴露于25 nM Et中,这段时间足以使膜受体位点不可逆地饱和,然后洗去未结合的Et。在这些条件下,观察到快速且短暂的收缩反应。它们不同于在肽持续存在时观察到的缓慢且不可逆的收缩。它们与氯化钾、血管紧张素II和血管加压素引起的收缩一样快。得出的结论是,Et收缩的不可逆性及其与受体的相互作用可以解偶联。数据还表明,内吞的Et受体的再循环有助于该肽的持续收缩作用。