Waen-Safranchik V I, Deth R C
Department of Pharmaceutical Sciences, Northeastern University, Boston, Mass. 02115.
Pharmacology. 1994 Jun;48(6):349-59. doi: 10.1159/000139200.
The inhibitory effect of wortmannin (WO), a fungus-derived protein kinase inhibitor, was assessed on contractile responses elicited by phenylephrine-induced alpha 1-(alpha 1 R) and UK 14304-induced alpha 2-adrenergic receptor (alpha 2R) stimulation in the rabbit aorta and saphenous vein, respectively. In agonist dose-response studies, WO caused a noncompetitive inhibition of both alpha 1R and alpha 2R responses, but was more potent against alpha 2R. Maximally effective single-dose responses at both receptors were less sensitive to WO. The initial alpha 1R contractile response, associated with intracellular Ca2+ release and myosin light chain kinase activation, was relatively insensitive to WO, while the Ca2+ influx-dependent tonic contraction was more sensitive. Contractions induced by high K+ buffer were relatively insensitive to WO in both the aorta and saphenous vein. These results indicate that WO inhibits receptor-initiated Ca2+ influx-dependent contractile responses such as those caused by alpha 2R stimulation and the sustained phase of alpha 1R stimulation more readily than Ca2+ release-dependent responses.
渥曼青霉素(WO)是一种源自真菌的蛋白激酶抑制剂,分别评估了其对苯肾上腺素诱导的α1 - 肾上腺素能受体(α1R)和UK 14304诱导的α2 - 肾上腺素能受体(α2R)刺激在兔主动脉和隐静脉中引发的收缩反应的抑制作用。在激动剂剂量反应研究中,WO对α1R和α2R反应均产生非竞争性抑制,但对α2R的作用更强。两种受体的最大有效单剂量反应对WO的敏感性较低。与细胞内Ca2 +释放和肌球蛋白轻链激酶激活相关的初始α1R收缩反应对WO相对不敏感,而Ca2 +内流依赖性强直收缩则更敏感。高K +缓冲液诱导的收缩在主动脉和隐静脉中对WO均相对不敏感。这些结果表明,WO比Ca2 +释放依赖性反应更易抑制受体启动的Ca2 +内流依赖性收缩反应,如α2R刺激和α1R刺激的持续阶段所引起的反应。