Vigne P, Lazdunski M, Frelin C
Centre de Biochimie, Centre National de la Recherche Scientifique, Nice, France.
FEBS Lett. 1989 Jun 5;249(2):143-6. doi: 10.1016/0014-5793(89)80611-8.
Endothelin-1 induces a positive inotropic response in isolated left atria of the rat with an IC50 value of 20 nM. The contractile effect of endothelin is larger than that of other inotropic hormones such as phenylephrine and epinephrine and smaller than that of Bay K8644. In the spontaneously active right atria, endothelin induces a positive inotropic effect with no chronotropic effect. Endothelin does not modify intracellular levels of cAMP under basal conditions or after stimulation with isoproterenol but stimulates the formation of inositol phosphates. Mobilization of inositol phospholipids is observed in the same range of concentrations as for the contractile action of endothelin. The contractile action of endothelin is not mediated by protein kinase C. It is antagonized by blockers of L-type Ca2+ channels, low external Ca2+ concentrations and drugs such as caffeine and ryanodine that interfere with Ca2+ release by the sarcoplasmic reticulum.
内皮素-1在大鼠离体左心房中可诱导正性肌力反应,半数抑制浓度(IC50)值为20 nM。内皮素的收缩作用大于其他正性肌力激素,如去氧肾上腺素和肾上腺素,小于Bay K8644。在自发活动的右心房中,内皮素可诱导正性肌力作用,而无变时作用。在基础条件下或用异丙肾上腺素刺激后,内皮素不会改变细胞内cAMP水平,但会刺激肌醇磷酸的形成。在与内皮素收缩作用相同的浓度范围内观察到肌醇磷脂的动员。内皮素的收缩作用不是由蛋白激酶C介导的。它可被L型钙通道阻滞剂、低细胞外钙浓度以及干扰肌浆网钙释放的药物(如咖啡因和ryanodine)所拮抗。